Inventario de la UE
Inventario de la UE
Aplicaciones anidadas
Inventario de la UE
The EC inventory published below is a copy as received from the JRC in 2008 on the founding of ECHA. It is comprised of the following lists:
- EINECS (European INventory of Existing Commercial chemical Substances) as published in O.J. C 146A, 15.6.1990. EINECS is an inventory of substances that were deemed to be on the European Community market between 1 January 1971 and 18 September 1981. EINECS was drawn up by the European Commission in the application of Article 13 of Directive 67/548/EEC, as amended by Directive 79/831/EEC, and in accordance with the detailed provisions of Commission Decision 81/437/EEC. Substances listed in EINECS are considered phase-in substances under the REACH Regulation.
- ELINCS (European LIst of Notified Chemical Substances) in support of Directive 92/32/EEC, the 7th amendment to Directive 67/548/EEC. ELINCS lists those substances which were notified under Directive 67/548/EEC, the Dangerous Substances Directive Notification of New Substances (NONS) that became commercially available after 18 September 1981.
- NLP (No-Longer Polymers). The definition of polymers was changed in April 1992 by Council Directive 92/32/EEC amending Directive 67/548/EEC, with the result that substances previously considered to be polymers were no longer excluded from regulation. Thus the No-longer Polymers (NLP) list was drawn up, consisting of such substances that were commercially available between 18 September 1981 and 31 October 1993.
Database contains 106212 unique substances/entries.
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The List does not contain any Substances.
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233-324-8
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10119-53-6
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C18H36O2.xCe
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Details | ||
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213-789-3
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1012-12-0
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C10H14O2Si
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Details | ||
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213-790-9
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1012-72-2
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C14H22
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Details | ||
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213-791-4
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1012-91-5
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C12H18N2
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Details | ||
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233-325-3
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10120-28-2
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C7D14
|
Details | ||
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309-813-8
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101200-45-7
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Details | |||
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309-814-3
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101200-46-8
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Details | |||
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309-815-9
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101200-47-9
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Details | |||
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401-190-1
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101200-48-0
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L5300
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Details | ||
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405-230-9
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101205-02-1
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CYCLOXYDIM
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Details | ||
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233-326-9
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10121-91-2
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C17H25N3O2S
|
Details | ||
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443-150-6
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101226-85-1
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ECS-ESTER
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Details | ||
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309-816-4
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101226-95-3
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Details | |||
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309-818-5
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101226-96-4
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Details | |||
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309-819-0
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101226-97-5
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Details | |||
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309-820-6
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101226-98-6
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Details | |||
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309-821-1
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101226-99-7
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Details | |||
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309-822-7
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101227-00-3
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Details | |||
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309-823-2
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101227-01-4
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Details | |||
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309-824-8
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101227-02-5
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Details | |||
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309-825-3
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101227-03-6
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Details | |||
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309-826-9
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101227-04-7
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Details | |||
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309-827-4
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101227-05-8
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Details | |||
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309-829-5
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101227-06-9
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Details | |||
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309-830-0
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101227-07-0
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Details | |||
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309-831-6
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101227-08-1
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Details | |||
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309-832-1
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101227-09-2
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Details | |||
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309-833-7
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101227-10-5
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Details | |||
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309-834-2
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101227-11-6
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Details | |||
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309-835-8
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101227-12-7
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Details | |||
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The oil obtained from the heat treatment of polystyrene with aromatic oils. It consists predominantly of naphthalene and its homologs, 1,3-diphenylpropane and other polynuclear aromatic hydrocarbons boiling in a range of approximately 200°C to 400°C (392°F to 752°F).
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309-836-3
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101227-13-8
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The oil obtained from the heat treatment of polystyrene with aromatic oils. It consists predominantly of naphthalene and its homologs, 1,3-diphenylpropane and other polynuclear aromatic hydrocarbons boiling in a range of approximately 200°C to 400°C (392°F to 752°F).
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Details | |
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The oil obtained from the heat treatment of polyethylene with aromatic oils. It consists predominantly of naphthalene and its homologs, 1,3-diphenylpropane and other polynuclear aromatic hydrocarbons boiling in a range of approximately 200°C to 400°C (392°F to 752°F).
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309-837-9
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101227-14-9
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The oil obtained from the heat treatment of polyethylene with aromatic oils. It consists predominantly of naphthalene and its homologs, 1,3-diphenylpropane and other polynuclear aromatic hydrocarbons boiling in a range of approximately 200°C to 400°C (392°F to 752°F).
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Details | |
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309-838-4
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101227-15-0
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Substance obtained by acidic, alkaline, or enzymatic hydrolysis of corynebacterium melassecola composed primarily of amino acids, peptides, and proteins. It may contain impurities consisting chiefly of carbohydrates and lipids along with smaller quantities of miscellaneous organic substances of biological origin.
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309-840-5
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101227-16-1
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Substance obtained by acidic, alkaline, or enzymatic hydrolysis of corynebacterium melassecola composed primarily of amino acids, peptides, and proteins. It may contain impurities consisting chiefly of carbohydrates and lipids along with smaller quantities of miscellaneous organic substances of biological origin.
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Details | |
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Substance obtained by acidic, alkaline, or enzymatic hydrolysis of methylophilus methylotrophus composed primarily of amino acids, peptides, and proteins. It may contain impurities consisting chiefly of carbohydrates and lipids along with smaller quantities of miscellaneous organic substances of biological origin.
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309-841-0
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101227-17-2
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Substance obtained by acidic, alkaline, or enzymatic hydrolysis of methylophilus methylotrophus composed primarily of amino acids, peptides, and proteins. It may contain impurities consisting chiefly of carbohydrates and lipids along with smaller quantities of miscellaneous organic substances of biological origin.
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Details | |
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The material having low solids concentration in water obtained by biological oxidation of wastewater from hydroxyethylcellulose manufacturing by aerobic or anaerobic paths.
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309-842-6
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101227-18-3
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The material having low solids concentration in water obtained by biological oxidation of wastewater from hydroxyethylcellulose manufacturing by aerobic or anaerobic paths.
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Details | |
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The material having low solids concentration in water obtained by biological oxidation of wastewater from rosin derivative manufacturing by aerobic or anaerobic paths.
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309-843-1
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101227-19-4
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The material having low solids concentration in water obtained by biological oxidation of wastewater from rosin derivative manufacturing by aerobic or anaerobic paths.
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Details | |
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Extractives and their physically modified derivatives such as proteins, carbohydrates, lipids, nucleic acids, inorganic ions, etc. obtained from Clupea sprattus.
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309-844-7
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101227-20-7
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Extractives and their physically modified derivatives such as proteins, carbohydrates, lipids, nucleic acids, inorganic ions, etc. obtained from Clupea sprattus.
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Details | |
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309-845-2
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101227-22-9
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309-846-8
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101227-23-0
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Details | |||
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The oil obtained from the pyrolysis of automobile shredder wastes at 600°C to 800°C (1112°F to 1472°F). It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C6 through C28, substituted aromatic hydrocarbons, heteroaromatics and other organic compounds boiling in the range of approximately 50°C to 500°C (122°F to 932°F).
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309-847-3
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101227-24-1
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The oil obtained from the pyrolysis of automobile shredder wastes at 600°C to 800°C (1112°F to 1472°F). It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C6 through C28, substituted aromatic hydrocarbons, heteroaromatics and other organic compounds boiling in the range of approximately 50°C to 500°C (122°F to 932°F).
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Details | |
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233-327-4
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10123-62-3
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C7H14NO3P
|
Details | ||
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233-329-5
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10124-29-5
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Al.xH2O4S
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Details | ||
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233-330-0
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10124-31-9
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H3N.xH3O4P
|
Details | ||
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233-331-6
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10124-36-4
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Cd.H2O4S
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Details | ||
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233-332-1
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10124-37-5
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Ca.2HNO3
|
Details | ||
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233-333-7
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10124-41-1
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Ca.H2O3S2
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233-334-2
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10124-43-3
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Co.H2O4S
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Details | ||
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233-335-8
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10124-48-8
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ClH2HgN
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Details | ||
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233-336-3
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10124-49-9
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Fe.xH2O4S
|
Details | ||
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233-337-9
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10124-50-2
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AsH3O3.xK
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Details | ||
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233-338-4
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10124-52-4
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H4O7P2.xK
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Details | ||
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233-340-5
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10124-53-5
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H2O3S2.Mg
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Details | ||
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233-341-0
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10124-54-6
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H3O4P.xMn
|
Details | ||
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233-342-6
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10124-55-7
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H2O4S.xMn
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Details | ||
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233-343-1
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10124-56-8
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H6O18P6.6Na
|
Details | ||
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233-344-7
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10124-65-9
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C12H24O2.K
|
Details | ||
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233-345-2
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10124-68-2
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C11H21NO
|
Details | ||
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233-346-8
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10124-98-8
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C10H16
|
Details | ||
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233-347-3
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10126-68-8
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C36H68O2
|
Details | ||
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233-348-9
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10126-87-1
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C20H18O10S4.2Na
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Details | ||
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233-349-4
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10126-90-6
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C29H18N2O17S4.4Na
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Details | ||
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233-351-5
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10126-92-8
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C18H13ClO9S4.2Na
|
Details | ||
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233-352-0
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10126-97-3
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C18H11Cl3O8S4.2Na
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Details | ||
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233-353-6
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10127-02-3
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C17H19N3.xCl2Zn.ClH
|
Details | ||
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233-354-1
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10127-03-4
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C48H36N6O6
|
Details | ||
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233-355-7
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10127-05-6
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C18H13CrN4O10S2.2Na
|
Details | ||
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233-356-2
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10127-06-7
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C43H28CuN9O13S3.3Na
|
Details | ||
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233-357-8
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10127-27-2
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C16H11CrN5O8S.Na
|
Details | ||
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233-358-3
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10127-36-3
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C17H21N4O.Cl
|
Details | ||
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233-359-9
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10128-36-6
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C10H15NO2
|
Details | ||
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233-360-4
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10128-55-9
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C24H16N2O4S
|
Details | ||
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233-362-5
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10129-44-9
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C8H10N.Br
|
Details | ||
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233-363-0
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10129-71-2
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C21H17N
|
Details | ||
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233-364-6
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10129-78-9
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C8H6Br2O3
|
Details | ||
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213-793-5
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1013-20-3
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C10H8N2O2.H3N
|
Details | ||
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213-794-0
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1013-22-5
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C12H18N2
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Details | ||
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213-795-6
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1013-25-8
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C12H18N2
|
Details | ||
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213-796-1
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1013-75-8
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C11H15NO2
|
Details | ||
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213-797-7
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1013-76-9
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C12H18N2
|
Details | ||
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440-870-2
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1013-88-3
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BPI
|
Details | ||
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233-365-1
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10130-29-7
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C24H20N4O5S2.Na
|
Details | ||
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233-366-7
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10130-48-0
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C25H22N4O10S3.2Na
|
Details | ||
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233-367-2
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10130-89-9
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C7H5ClO4S
|
Details | ||
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233-368-8
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10131-46-1
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C13H13N
|
Details | ||
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478-380-6
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1013116-84-1
|
Details | |||
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309-848-9
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101316-43-2
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Details | |||
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309-849-4
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101316-44-3
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Details | |||
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A complex combination of hydrocarbons obtained as a redistillate from the distillation of wash oil. It consists predominantly of 2-ringed aromatic and heterocyclic hydrocarbons boiling in the range of approximately 260°C to 290°C (500°F to 554°F).
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309-851-5
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101316-45-4
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A complex combination of hydrocarbons obtained as a redistillate from the distillation of wash oil. It consists predominantly of 2-ringed aromatic and heterocyclic hydrocarbons boiling in the range of approximately 260°C to 290°C (500°F to 554°F).
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Details | |
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309-852-0
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101316-46-5
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Details | |||
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309-854-1
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101316-48-7
|
Details | |||
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The oil obtained from condensation of the vapors from the heat treatment of pitch. Composed primarily of two- to four-ring aromatic compounds boiling in the range of 200°C to greater than 400°C (392°F to greater than 752°F).
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309-855-7
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101316-49-8
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The oil obtained from condensation of the vapors from the heat treatment of pitch. Composed primarily of two- to four-ring aromatic compounds boiling in the range of 200°C to greater than 400°C (392°F to greater than 752°F).
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Details | |
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A complex combination of hydrocarbons obtained by the distillation of residual oils obtained during the pyrolytic production of alkenes and alkynes from petroleum products or natural gas. It consists predominantly of aromatic hydrocarbons having two and three rings and boiling in the range of approximately 230°C to 310°C (446°F to 590°F).
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309-856-2
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101316-50-1
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A complex combination of hydrocarbons obtained by the distillation of residual oils obtained during the pyrolytic production of alkenes and alkynes from petroleum products or natural gas. It consists predominantly of aromatic hydrocarbons having two and three rings and boiling in the range of approximately 230°C to 310°C (446°F to 590°F).
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Details | |
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A complex combination of hydrocarbons obtained by the distillation of residual oils obtained during the pyrolytic production of alkenes and alkynes from petroleum products or natural gas. It consists predominantly of aromatic hydrocarbons having three or more rings and boiling in the range of approximately 270°C to 420°C (518°F to 788°F).
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309-857-8
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101316-51-2
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A complex combination of hydrocarbons obtained by the distillation of residual oils obtained during the pyrolytic production of alkenes and alkynes from petroleum products or natural gas. It consists predominantly of aromatic hydrocarbons having three or more rings and boiling in the range of approximately 270°C to 420°C (518°F to 788°F).
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Details | |
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A complex combination of hydrocarbons obtained by the distillation of residual oils obtained during the pyrolytic production of alkenes and alkynes from petroleum products or natural gas. It consists predominantly of substituted aromatic hydrocarbons having two or more rings and boiling in the range of 225°C to 255°C (437°F to 491°F).
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309-858-3
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101316-52-3
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A complex combination of hydrocarbons obtained by the distillation of residual oils obtained during the pyrolytic production of alkenes and alkynes from petroleum products or natural gas. It consists predominantly of substituted aromatic hydrocarbons having two or more rings and boiling in the range of 225°C to 255°C (437°F to 491°F).
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Details | |
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A complex combination of hydrocarbons obtained by the distillation of residual oils obtained during the pyrolytic production of alkenes and alkynes from petroleum products or natural gas. It consists predominantly of aromatic hydrocarbons having two or more rings and boiling in the range of approximately 210°C to 225°C (410°F to 437°F).
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309-859-9
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101316-53-4
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A complex combination of hydrocarbons obtained by the distillation of residual oils obtained during the pyrolytic production of alkenes and alkynes from petroleum products or natural gas. It consists predominantly of aromatic hydrocarbons having two or more rings and boiling in the range of approximately 210°C to 225°C (410°F to 437°F).
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Details | |
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A complex combination of alkylbenzenes obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists predominantly of alkylbenzenes having carbon numbers predominantly in the range of C12 through C14 and boiling in the range of 200°C to 250°C (392°F to 482°F).
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309-860-4
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101316-54-5
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A complex combination of alkylbenzenes obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists predominantly of alkylbenzenes having carbon numbers predominantly in the range of C12 through C14 and boiling in the range of 200°C to 250°C (392°F to 482°F).
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Details | |
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A complex combination of hydrocarbons obtained by the distillation of petroleum light fraction, hydrodesulfurized and dearomatized. It consists predominantly of hydrocarbons having carbon numbers in the range of C7 through C9, predominantly C8 paraffins and cycloparaffins, boiling in the range of approximately 120°C to 130°C (248°F to 266°F).
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309-862-5
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101316-56-7
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A complex combination of hydrocarbons obtained by the distillation of petroleum light fraction, hydrodesulfurized and dearomatized. It consists predominantly of hydrocarbons having carbon numbers in the range of C7 through C9, predominantly C8 paraffins and cycloparaffins, boiling in the range of approximately 120°C to 130°C (248°F to 266°F).
|
Details | |
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A complex combination of hydrocarbons obtained by treating a petroleum stock with hydrogen. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C9 through C25 and boiling in the range of approximately 150°C to 400°C (302°F to 752°F).
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309-863-0
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101316-57-8
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A complex combination of hydrocarbons obtained by treating a petroleum stock with hydrogen. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C9 through C25 and boiling in the range of approximately 150°C to 400°C (302°F to 752°F).
|
Details | |
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A complex combination of hydrocarbons obtained by fractionation from hydrodesulphurised coker distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C8 through C16 and boiling in the range of approximately 120°C to 283°C (248°F to 541°F).
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309-864-6
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101316-58-9
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A complex combination of hydrocarbons obtained by fractionation from hydrodesulphurised coker distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C8 through C16 and boiling in the range of approximately 120°C to 283°C (248°F to 541°F).
|
Details | |
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A complex combination of hydrocarbons obtained by fractionation from hydrodesulphurised coker distillate stocks. It consists of hydrocarbons having carbon numbers predominantly in the range of C12 through C21 and boiling in the range of approximately 200°C to 360°C (392°F to 680°F).
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309-865-1
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101316-59-0
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A complex combination of hydrocarbons obtained by fractionation from hydrodesulphurised coker distillate stocks. It consists of hydrocarbons having carbon numbers predominantly in the range of C12 through C21 and boiling in the range of approximately 200°C to 360°C (392°F to 680°F).
|
Details | |
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A complex combination of hydrocarbons obtained by distillation of thermal-cracking heavy tars. It consists predominantly of highly alkylated aromatic hydrocarbons boiling in the range of approximately 100°C to 250°C (212°F to 482°F).
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309-866-7
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101316-61-4
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A complex combination of hydrocarbons obtained by distillation of thermal-cracking heavy tars. It consists predominantly of highly alkylated aromatic hydrocarbons boiling in the range of approximately 100°C to 250°C (212°F to 482°F).
|
Details | |
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309-867-2
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101316-62-5
|
Details | |||
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A complex combination of hydrocarbons obtained by the redistillation of the distillate of high temperature coal tar (tar acid and tar base free). It consists predominantly of unsubstituted and substituted mononuclear aromatic hydrocarbons boiling in the range of 85°C-195°C (185°F-383°F).
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309-868-8
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101316-63-6
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A complex combination of hydrocarbons obtained by the redistillation of the distillate of high temperature coal tar (tar acid and tar base free). It consists predominantly of unsubstituted and substituted mononuclear aromatic hydrocarbons boiling in the range of 85°C-195°C (185°F-383°F).
|
Details | |
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A complex combination of chemical compounds separated from steam cracker gas by scrubbing with diethanolamine. It consists predominantly of hydrogen sulfide and carbon dioxide.
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309-869-3
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101316-64-7
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A complex combination of chemical compounds separated from steam cracker gas by scrubbing with diethanolamine. It consists predominantly of hydrogen sulfide and carbon dioxide.
|
Details | |
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A complex combination of hydrocarbons obtained during the sorptions of toluene from a hydrocarbon fraction from cracked gasoline treated with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C8 and boiling in the range of approximately 80°C to 135°C (176°F to 275°F).
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309-870-9
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101316-66-9
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A complex combination of hydrocarbons obtained during the sorptions of toluene from a hydrocarbon fraction from cracked gasoline treated with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C8 and boiling in the range of approximately 80°C to 135°C (176°F to 275°F).
|
Details | |
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A complex combination of hydrocarbons obtained by distillation of hydrotreated naphtha followed by solvent extraction. It consists predominantly of saturated hydrocarbons and boiling in the range of approximately 65°C to 70°C (149°F to 158°F).
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309-871-4
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101316-67-0
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A complex combination of hydrocarbons obtained by distillation of hydrotreated naphtha followed by solvent extraction. It consists predominantly of saturated hydrocarbons and boiling in the range of approximately 65°C to 70°C (149°F to 158°F).
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Details | |
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A complex combination of alkylbenzenes obtained by the catalytic reforming of kerosine. It consists predominantly of alkylbenzenes having carbon numbers predominantly in the range of C8 through C15 and boiling in the range of approximately 160°C to 260°C (320°F to 500°F).
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309-873-5
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101316-68-1
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A complex combination of alkylbenzenes obtained by the catalytic reforming of kerosine. It consists predominantly of alkylbenzenes having carbon numbers predominantly in the range of C8 through C15 and boiling in the range of approximately 160°C to 260°C (320°F to 500°F).
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Details | |
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A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of vacuum distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C25 and produces a finished oil with a viscosity in the order of 32cSt to 37cSt at 100°C (212°F).
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309-874-0
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101316-69-2
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A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of vacuum distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C25 and produces a finished oil with a viscosity in the order of 32cSt to 37cSt at 100°C (212°F).
|
Details | |
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A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of atmospheric distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C32 and produces a finished oil with a viscosity in the order of 17cSt to 23cSt at 40°C (104°F).
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309-875-6
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101316-70-5
|
A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of atmospheric distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C32 and produces a finished oil with a viscosity in the order of 17cSt to 23cSt at 40°C (104°F).
|
Details | |
|
A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of atmospheric distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C35 and produces a finished oil with a viscosity in the order of 37cSt to 44cSt at 40°C (104°F).
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309-876-1
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101316-71-6
|
A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of atmospheric distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C35 and produces a finished oil with a viscosity in the order of 37cSt to 44cSt at 40°C (104°F).
|
Details | |
|
A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of atmospheric distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C24 through C50 and produces a finished oil with a viscosity in the order of 16cSt to 75cSt at 40°C (104°F).
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309-877-7
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101316-72-7
|
A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of atmospheric distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C24 through C50 and produces a finished oil with a viscosity in the order of 16cSt to 75cSt at 40°C (104°F).
|
Details | |
|
A complex combination of hydrocarbons obtained by refining waste oils without catalytic treatment with hydrogen. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100°F (19cSt at 40°C).
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309-878-2
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101316-73-8
|
A complex combination of hydrocarbons obtained by refining waste oils without catalytic treatment with hydrogen. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100°F (19cSt at 40°C).
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Details | |
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A complex combination of hydrocarbons obtained by fractionation from hydrodesulphurised coker distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 to C11 and boiling in the range of approximately 23°C to 196°C (73°F to 385°F).
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309-879-8
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101316-76-1
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A complex combination of hydrocarbons obtained by fractionation from hydrodesulphurised coker distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 to C11 and boiling in the range of approximately 23°C to 196°C (73°F to 385°F).
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Details | |
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309-880-3
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101316-78-3
|
Details | |||
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A complex combination of hydrocarbons obtained by the distillation of hydrocracked petroleum distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 235°C to 290°C (455°F to 554°F).
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309-881-9
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101316-80-7
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A complex combination of hydrocarbons obtained by the distillation of hydrocracked petroleum distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 235°C to 290°C (455°F to 554°F).
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Details | |
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A complex combination of hydrocarbons obtained by the catalytic hydrodesulfurization of a petroleum fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C10 through C13 and boiling in the range of approximately 180°C to 240°C (356°F to 464°F).
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309-882-4
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101316-81-8
|
A complex combination of hydrocarbons obtained by the catalytic hydrodesulfurization of a petroleum fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C10 through C13 and boiling in the range of approximately 180°C to 240°C (356°F to 464°F).
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Details | |
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A complex combination of hydrocarbons obtained by the catalytic hydrodesulfurization of a petroleum fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C10 through C13 and boiling in the range of approximately 175°C to 220°C (347°F to 428°F).
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309-884-5
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101316-82-9
|
A complex combination of hydrocarbons obtained by the catalytic hydrodesulfurization of a petroleum fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C10 through C13 and boiling in the range of approximately 175°C to 220°C (347°F to 428°F).
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Details | |
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An oil distilled from brown-coal tar. Composed primarily of aliphatic, naphthenic and one- to three-ring aromatic hydrocarbons, their alkyl derivatives, heteroaromatics and one- and two-ring phenols boiling in the range of approximately 150°C to 360°C (302°F to 680°F).
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309-885-0
|
101316-83-0
|
An oil distilled from brown-coal tar. Composed primarily of aliphatic, naphthenic and one- to three-ring aromatic hydrocarbons, their alkyl derivatives, heteroaromatics and one- and two-ring phenols boiling in the range of approximately 150°C to 360°C (302°F to 680°F).
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Details | |
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A tar obtained from low temperature carbonization and low temperature gasification of brown coal. Composed primarily of aliphatic, naphthenic and cyclic aromatic hydrocarbons, heteroaromatic hydrocarbons and cyclic phenols.
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309-886-6
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101316-84-1
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A tar obtained from low temperature carbonization and low temperature gasification of brown coal. Composed primarily of aliphatic, naphthenic and cyclic aromatic hydrocarbons, heteroaromatic hydrocarbons and cyclic phenols.
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Details | |
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Residues from fractional distillation of low temperature coal tar to remove oils that boil in a range up to approximately 300°C (572°F). Composed primarily of aromatic compounds.
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309-887-1
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101316-85-2
|
Residues from fractional distillation of low temperature coal tar to remove oils that boil in a range up to approximately 300°C (572°F). Composed primarily of aromatic compounds.
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Details | |
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An acidified alkaline extract of brown coal tar distillate. Composed primarily of phenol and phenol homologs.
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309-888-7
|
101316-86-3
|
An acidified alkaline extract of brown coal tar distillate. Composed primarily of phenol and phenol homologs.
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Details | |
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A distillate from low-temperature coal tar. Composed primarily of hydrocarbons, phenolic compounds and aromatic nitrogen bases boiling in the range of approximately 160°C to 340°C (320°F to 644°F).
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309-889-2
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101316-87-4
|
A distillate from low-temperature coal tar. Composed primarily of hydrocarbons, phenolic compounds and aromatic nitrogen bases boiling in the range of approximately 160°C to 340°C (320°F to 644°F).
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Details | |
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233-369-3
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10132-07-7
|
C4H3Cl2N3
|
Details | ||
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233-370-9
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10132-80-6
|
C28H18N4O3S4.Na
|
Details | ||
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233-371-4
|
10132-98-6
|
C16H10ClN3O7S.Na
|
Details | ||
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233-373-5
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10132-99-7
|
C16H12ClN5O7S.Na
|
Details | ||
|
500-286-1
|
101325-00-2
|
Details | |||
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233-374-0
|
10134-33-5
|
C36H25N7O10S3.3Na
|
Details | ||
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233-375-6
|
10134-35-7
|
C20H11BrClNO8S3.2Na
|
Details | ||
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309-890-8
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101356-94-9
|
Details | |||
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309-891-3
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101356-95-0
|
Details | |||
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309-892-9
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101356-96-1
|
Details | |||
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309-893-4
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101356-97-2
|
Details | |||
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309-895-5
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101356-98-3
|
Details | |||
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309-896-0
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101356-99-4
|
Details | |||
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309-897-6
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101357-00-0
|
Details | |||
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309-898-1
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101357-01-1
|
Details | |||
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309-899-7
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101357-02-2
|
Details | |||
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309-900-0
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101357-03-3
|
Details | |||
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309-901-6
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101357-04-4
|
Details | |||
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309-902-1
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101357-05-5
|
Details | |||
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309-903-7
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101357-06-6
|
Details | |||
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309-904-2
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101357-07-7
|
Details | |||
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309-905-8
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101357-08-8
|
Details | |||
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309-906-3
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101357-09-9
|
Details | |||
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309-907-9
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101357-10-2
|
Details | |||
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309-908-4
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101357-11-3
|
Details | |||
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309-910-5
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101357-12-4
|
Details | |||
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309-911-0
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101357-13-5
|
Details | |||
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309-912-6
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101357-15-7
|
Details | |||
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309-913-1
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101357-16-8
|
Details | |||
|
309-914-7
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101357-17-9
|
Details | |||
|
309-915-2
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101357-18-0
|
Details | |||
|
309-916-8
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101357-19-1
|
Details | |||
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309-917-3
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101357-20-4
|
Details | |||
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309-918-9
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101357-21-5
|
Details | |||
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309-919-4
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101357-22-6
|
Details | |||
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309-921-5
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101357-23-7
|
Details | |||
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309-922-0
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101357-24-8
|
Details | |||
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309-923-6
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101357-25-9
|
Details | |||
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309-924-1
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101357-26-0
|
Details | |||
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309-925-7
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101357-27-1
|
Details | |||
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309-926-2
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101357-28-2
|
Details | |||
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309-927-8
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101357-29-3
|
Details | |||
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309-928-3
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101357-30-6
|
Details | |||
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309-929-9
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101357-31-7
|
Details | |||
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309-930-4
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101357-32-8
|
Details | |||
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309-932-5
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101357-33-9
|
Details | |||
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309-933-0
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101357-35-1
|
Details | |||
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233-376-1
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10136-65-9
|
C10H16O2
|
Details | ||
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233-377-7
|
10137-69-6
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C6H9Cl3Si
|
Details | ||
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233-378-2
|
10137-74-3
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Ca.2ClHO3
|
Details | ||
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233-379-8
|
10137-90-3
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C11H20O
|
Details | ||
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309-934-6
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101377-33-7
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C33H58O18
|
Details | ||
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309-935-1
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101377-34-8
|
C24H42O13
|
Details | ||
|
233-380-3
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10138-01-9
|
Eu.3HNO3
|
Details | ||
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233-381-9
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10138-02-0
|
C14H30N2O
|
Details | ||
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233-382-4
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10138-04-2
|
Fe.H3N.2H2O4S
|
Details | ||
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233-384-5
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10138-21-3
|
C4H8Cl2Si
|
Details | ||
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430-700-5
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10138-36-0
|
SANSOCIZER E-PS
|
Details | ||
|
233-385-0
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10138-41-7
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Cl3Er
|
Details | ||
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233-386-6
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10138-52-0
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Cl3Gd
|
Details | ||
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233-387-1
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10138-62-2
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Cl3Ho
|
Details | ||
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233-388-7
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10138-79-1
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C6H13Cl3O3Si
|
Details | ||
|
233-389-2
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10138-93-9
|
C6H15N.xH3O4P
|
Details | ||
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233-390-8
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10138-94-0
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C4H6O6U.Zn
|
Details | ||
|
233-391-3
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10139-01-2
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C14H18N2O8
|
Details | ||
|
233-392-9
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10139-02-3
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C14H18N2O8
|
Details | ||
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233-393-4
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10139-04-5
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C14H19NO6
|
Details | ||
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233-395-5
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10139-18-1
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C6H14O12P2
|
Details | ||
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233-396-0
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10139-47-6
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I2Zn
|
Details | ||
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233-397-6
|
10139-58-9
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HNO3.1/3Rh
|
Details | ||
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213-798-2
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1014-05-7
|
C12H18N2
|
Details | ||
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213-799-8
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1014-66-0
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C9H13NO3Si
|
Details | ||
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213-800-1
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1014-69-3
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C8H15N5S
|
Details | ||
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213-801-7
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1014-70-6
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C8H15N5S
|
Details | ||
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213-802-2
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1014-81-9
|
C8H5F3O3
|
Details | ||
|
233-398-1
|
10140-87-1
|
C4H6Cl2O2
|
Details | ||
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233-399-7
|
10140-89-3
|
C3H4Cl2O
|
Details | ||