EG-förteckningen

EG-förteckningen

Kapslade applikationer

EG-förteckningen

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.
 
233-400-0
10140-96-2
C8H15ClO2
Details
309-936-7
101403-98-9
Details
PROJET 780 NP; SUBSTANCE SC101756
407-700-9
101408-30-4
PROJET 780 NP; SUBSTANCE SC101756
Details
233-401-6
10141-00-1
Cr.2H2O4S.K
Details
233-402-1
10141-05-6
Co.2HNO3
Details
233-403-7
10142-37-7
C14H13N3O3.Na
Details
233-404-2
10142-78-6
C37H27N5O6S2.2Na
Details
233-405-8
10143-03-0
C25H25NO6
Details
233-406-3
10143-07-4
C13H10N2O3.Na
Details
233-407-9
10143-22-3
C6H13NO5
Details
233-408-4
10143-32-5
C8H18O3
Details
233-410-5
10143-38-1
Dy.3HNO3
Details
233-411-0
10143-53-0
C8H16O3
Details
233-412-6
10143-60-9
C16H34O
Details
233-413-1
10144-81-7
C30H20N4O4
Details
FLUFENOXURON
417-680-3
101463-69-8
FLUFENOXURON
Details
233-414-7
10147-36-1
C3H7ClO2S
Details
233-415-2
10147-37-2
C3H7ClO2S
Details
233-416-8
10147-40-7
C12H25ClO2S
Details
233-417-3
10147-41-8
C18H37ClO2S
Details
233-418-9
10149-98-1
C18H16N4O12S3
Details
213-803-8
1015-55-0
C12H14O3
Details
213-804-3
1015-89-0
C13H9NO
Details
309-937-2
101500-43-0
Details
233-419-4
10151-02-7
C9H19NO
Details
233-421-5
10151-78-7
C10H13NO2
Details
3,5-DICHLORO-2,4-DIFLUOROBENZOYLFLUORIDE
401-800-6
101513-70-6
3,5-DICHLORO-2,4-DIFLUOROBENZOYLFLUORIDE
Details
233-422-0
10152-76-8
C4H8S
Details
451-260-0
10152-77-9
CORPS TRUFFE
Details
233-423-6
10153-83-0
C9H14O4
Details
233-424-1
10154-75-3
C9H9NO2S
Details
233-425-7
10154-97-9
C13H12O4
Details
233-426-2
10155-47-2
C18H22N2O3
Details
233-427-8
10155-48-3
C18H21BrN2O3
Details
233-428-3
10155-49-4
C19H24N2O4
Details
233-429-9
10155-52-9
C19H17ClN6O5
Details
213-805-9
1016-05-3
C12H8O2S
Details
213-806-4
1016-58-6
C9H11NO5
Details
213-808-5
1016-77-9
C13H9BrO
Details
213-809-0
1016-78-0
C13H9ClO
Details
233-430-4
10160-87-9
C7H12O2
Details
233-432-5
10161-34-9
C20H24O3
Details
233-433-0
10163-15-2
FH2O3P.2Na
Details
233-434-6
10163-62-9
C8H19O3PS
Details
A complex combination of hydrocarbons obtained by distillation of catalytic 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).
309-938-8
101631-13-4
A complex combination of hydrocarbons obtained by distillation of catalytic 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
A complex combination of hydrocarbons obtained by distillation of steam cracking heavy residues. It consists predominantly of highly alkylated heavy aromatic hydrocarbons boiling in the range of approximately 250°C to 400°C (482°F to 752°F).
309-939-3
101631-14-5
A complex combination of hydrocarbons obtained by distillation of steam cracking heavy residues. It consists predominantly of highly alkylated heavy aromatic hydrocarbons boiling in the range of approximately 250°C to 400°C (482°F to 752°F).
Details
A complex combination of hydrocarbons obtained by distillation of steam 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).
309-940-9
101631-15-6
A complex combination of hydrocarbons obtained by distillation of steam 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
309-941-4
101631-17-8
Details
The recovered oil obtained by skimming all plant oil bearing water streams. It consists predominantly of lubricating oil, oil additives and intermediates.
309-943-5
101631-18-9
The recovered oil obtained by skimming all plant oil bearing water streams. It consists predominantly of lubricating oil, oil additives and intermediates.
Details
A complex combination of hydrocarbons obtained from the distillation of petroleum and subsequent hydrotreatment. It consists predominantly of alkanes, cycloalkanes and alkylbenzenes having carbon numbers predominantly in the range of C12 through C16 and boiling in the range of approximately 230°C to 270°C (446°F to 518°F).
309-944-0
101631-19-0
A complex combination of hydrocarbons obtained from the distillation of petroleum and subsequent hydrotreatment. It consists predominantly of alkanes, cycloalkanes and alkylbenzenes having carbon numbers predominantly in the range of C12 through C16 and boiling in the range of approximately 230°C to 270°C (446°F to 518°F).
Details
A complex combination of hydrocarbons obtained from a distillation process of crude petroleum. It consists predominantly of hydrocarbons having carbon numbers in the range of C8 through C12 and boiling in the range of approximately 130°C to 210°C (266°F to 410°F).
309-945-6
101631-20-3
A complex combination of hydrocarbons obtained from a distillation process of crude petroleum. It consists predominantly of hydrocarbons having carbon numbers in the range of C8 through C12 and boiling in the range of approximately 130°C to 210°C (266°F to 410°F).
Details
A complex combination of compounds obtained by the fractional distillation of residual oils which are obtained during the pyrolytic recovery of alkenes and alkynes from mineral oil products or natural gas. It consists predominantly of mono- and dinuclear aromatic hydrocarbons boiling in the range of approximately 130°C to 215°C (266°F to 419°F).
309-946-1
101631-21-4
A complex combination of compounds obtained by the fractional distillation of residual oils which are obtained during the pyrolytic recovery of alkenes and alkynes from mineral oil products or natural gas. It consists predominantly of mono- and dinuclear aromatic hydrocarbons boiling in the range of approximately 130°C to 215°C (266°F to 419°F).
Details
309-947-7
101631-22-5
Details
309-948-2
101631-23-6
Details
309-949-8
101631-24-7
Details
309-950-3
101631-25-8
Details
233-435-1
10164-64-4
C9H24BN3O3
Details
AROCY M-10
405-790-4
101657-77-6
AROCY M-10
Details
UC-132
406-840-8
101664-25-9
UC-132
Details
233-436-7
10168-80-6
Er.3HNO3
Details
233-437-2
10168-81-7
Gd.3HNO3
Details
233-438-8
10168-82-8
HNO3.1/3Ho
Details
233-439-3
10169-02-5
C32H22N4O8S2.2Na
Details
233-440-9
10169-29-6
C42H24N2O24S6.6Na
Details
233-441-4
10169-52-5
C20H12ClNO8S3.2Na
Details
233-443-5
10169-55-8
C14H12OS
Details
484-020-9
1016902-02-5
Details
471-980-9
1016986-95-0
Details
213-810-6
1017-56-7
C6H12N6O3
Details
233-444-0
10170-03-3
C48H54N4O16
Details
233-445-6
10170-69-1
C10Mn2O10
Details
233-446-1
10171-38-7
C3H8O2
Details
426-370-7
1017183-70-8
SOLE 3
Details
233-447-7
10172-89-1
C11H13NO3
Details
233-448-2
10175-15-2
C7H16MgO
Details
233-449-8
10175-95-8
C19H33O4P.1/2Zn
Details
233-450-3
10176-39-3
C46H64O19
Details
309-951-9
101794-70-1
Details
A complex combination of hydrocarbons obtained from mixed aromatic oil-polyethylene-polypropylene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 30°C to 140°C (86°F to 184°F) according to DIN 52025.
309-952-4
101794-71-2
A complex combination of hydrocarbons obtained from mixed aromatic oil-polyethylene-polypropylene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 30°C to 140°C (86°F to 184°F) according to DIN 52025.
Details
A complex combination of hydrocarbons obtained from mixed aromatic oil-polyethylene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 30°C to 140°C (86°F to 284°F) according to DIN 52025.
309-954-5
101794-72-3
A complex combination of hydrocarbons obtained from mixed aromatic oil-polyethylene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 30°C to 140°C (86°F to 284°F) according to DIN 52025.
Details
A complex combination of hydrocarbons obtained from mixed aromatic oil-polystyrene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 30°C to 140°C (86°F to 284°F) according to DIN 52025.
309-955-0
101794-73-4
A complex combination of hydrocarbons obtained from mixed aromatic oil-polystyrene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 30°C to 140°C (86°F to 284°F) according to DIN 52025.
Details
A complex combination hydrocarbons obtained from mixed coal tar pitch-polyethylene-polypropylene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 100°C to 220°C (212°F to 428°F) according to DIN 52025.
309-956-6
101794-74-5
A complex combination hydrocarbons obtained from mixed coal tar pitch-polyethylene-polypropylene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 100°C to 220°C (212°F to 428°F) according to DIN 52025.
Details
A complex combination of hydrocarbons obtained from mixed coal tar pitch-polyethylene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 100°C to 220°C (212°F to 428°F) according to DIN 52025.
309-957-1
101794-75-6
A complex combination of hydrocarbons obtained from mixed coal tar pitch-polyethylene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 100°C to 220°C (212°F to 428°F) according to DIN 52025.
Details
A complex combination of hydrocarbons obtained from mixed coal tar pitch-polystyrene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 100°C to 220°C (212°F to 428°F) according to DIN 52025.
309-958-7
101794-76-7
A complex combination of hydrocarbons obtained from mixed coal tar pitch-polystyrene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 100°C to 220°C (212°F to 428°F) according to DIN 52025.
Details
309-959-2
101794-77-8
Details
309-960-8
101794-78-9
Details
The dusts from an electrostatic filter obtained during the combustion of waste substances from the preparation of acrylonitrile according to the Sohio process. Composed primarily of carbonates and sulfates of antimony and molybdenum.
309-961-3
101794-79-0
The dusts from an electrostatic filter obtained during the combustion of waste substances from the preparation of acrylonitrile according to the Sohio process. Composed primarily of carbonates and sulfates of antimony and molybdenum.
Details
309-962-9
101794-80-3
Details
Extractives and their physically modified derivatives such as proteins, carbohydrates, lipids, nucleic acids, inorganic ions, etc. obtained from Protaminobacter ruber, Methylomonadaceae.
309-963-4
101794-81-4
Extractives and their physically modified derivatives such as proteins, carbohydrates, lipids, nucleic acids, inorganic ions, etc. obtained from Protaminobacter ruber, Methylomonadaceae.
Details
Substance obtained by acidic, alkaline, or enzymatic hydrolysis of fusarium graminearum 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.
309-965-5
101794-82-5
Substance obtained by acidic, alkaline, or enzymatic hydrolysis of fusarium graminearum 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.
Details
309-966-0
101794-83-6
Details
309-967-6
101794-84-7
Details
309-968-1
101794-85-8
Details
309-969-7
101794-86-9
Details
The dilute aqueous solution condensed from the gas evolved in the low-temperature destructive distillation of coal. Composed primarily of ammonium carbonate and other ammonium salts.
309-970-2
101794-87-0
The dilute aqueous solution condensed from the gas evolved in the low-temperature destructive distillation of coal. Composed primarily of ammonium carbonate and other ammonium salts.
Details
A distillate from the fractional distillation of high temperature coal tar. Composed primarily of alkyl-substituted one ring aromatic hydrocarbons boiling in the range of approximately 135°C to 210°C (275°F to 410°F). May also include unsaturated hydrocarbons such as indene and coumarone.
309-971-8
101794-90-5
A distillate from the fractional distillation of high temperature coal tar. Composed primarily of alkyl-substituted one ring aromatic hydrocarbons boiling in the range of approximately 135°C to 210°C (275°F to 410°F). May also include unsaturated hydrocarbons such as indene and coumarone.
Details
A distillate from the fractional distillation of high temperature coal tar. Composed primarily of indole and methylnaphthalene boiling in the range of approximately 235°C to 255°C (455°F to 491°F).
309-972-3
101794-91-6
A distillate from the fractional distillation of high temperature coal tar. Composed primarily of indole and methylnaphthalene boiling in the range of approximately 235°C to 255°C (455°F to 491°F).
Details
A complex combination of compounds obtained by catalytic hot air oxidation of a petroleum fraction having carbon numbers predominantly in the range of C19 through C40 and boiling in the range of approximately 390°C to 550°C (734°F to 1022°F).
309-973-9
101794-94-9
A complex combination of compounds obtained by catalytic hot air oxidation of a petroleum fraction having carbon numbers predominantly in the range of C19 through C40 and boiling in the range of approximately 390°C to 550°C (734°F to 1022°F).
Details
A complex combination of hydrocarbons obtained by distillation of products from a catalytic cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C8 through C12 and boiling in the range of approximately 140°C to 210°C (284°F to 410°F).
309-974-4
101794-97-2
A complex combination of hydrocarbons obtained by distillation of products from a catalytic cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C8 through C12 and boiling in the range of approximately 140°C to 210°C (284°F to 410°F).
Details
A complex combination of hydrocarbons obtained by subjecting a petroleum naphtha to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C8 and boiling in the range of approximately 20°C to 130°C (68°F to 266°F).
309-976-5
101795-01-1
A complex combination of hydrocarbons obtained by subjecting a petroleum naphtha to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C8 and boiling in the range of approximately 20°C to 130°C (68°F to 266°F).
Details
By-products obtained from treatment of phosphate rock with phosphoric acid, caustic soda and other chemicals in the purification of phosphoric acid for technical phosphate production.
309-977-0
101795-04-4
By-products obtained from treatment of phosphate rock with phosphoric acid, caustic soda and other chemicals in the purification of phosphoric acid for technical phosphate production.
Details
213-811-1
1018-36-6
C10H13N3O2S
Details
213-812-7
1018-71-9
C10H6Cl2N2O2
Details
233-451-9
10181-37-0
C19H15N3.HNO3
Details
233-452-4
10181-46-1
C17H9NO4.2H2O3S.2Na
Details
309-978-6
101810-92-8
C21H32N4O4
Details
233-454-5
10182-92-0
C17H38N
Details
233-455-0
10183-49-0
C14H8Cl2O4
Details
309-979-1
101836-91-3
C32H20CrN8O8.H4N
Details
233-456-6
10184-66-4
C4H11O4P
Details
233-457-1
10187-52-7
C13H10Cl2O2.Na
Details
233-458-7
10189-42-1
C23H26Cl2N5O2S.Cl
Details
309-980-7
101896-21-3
C19H24F19N2O8P
Details
309-981-2
101896-22-4
C26H18F38NO6P
Details
309-982-8
101896-23-5
C15H30O
Details
309-983-3
101896-25-7
C20H26N3O.ClO4
Details
A residue from the distillation of crude benzole to remove benzole fronts. Composed primarily of benzene, toluene and xylenes boiling in the range of approximately 75°C to 200°C (167°F to 392°F).
309-984-9
101896-26-8
A residue from the distillation of crude benzole to remove benzole fronts. Composed primarily of benzene, toluene and xylenes boiling in the range of approximately 75°C to 200°C (167°F to 392°F).
Details
A distillate from the fractional distillation of high temperature coal tar. Composed primarily of substituted two ring aromatic hydrocarbons and aromatic nitrogen bases boiling in the range of approximately 225°C to 255°C (437°F to 491°F).
309-985-4
101896-27-9
A distillate from the fractional distillation of high temperature coal tar. Composed primarily of substituted two ring aromatic hydrocarbons and aromatic nitrogen bases boiling in the range of approximately 225°C to 255°C (437°F to 491°F).
Details
309-987-5
101896-28-0
Details
309-988-0
101896-29-1
Details
Extractives and their physically modified derivatives such as tinctures, concretes, absolutes, essential oils, oleoresins, terpenes, terpene-free fractions, distillates, residues, etc., obtained from Polygala paucifolia, Polygalaceae.
309-989-6
101896-30-4
Extractives and their physically modified derivatives such as tinctures, concretes, absolutes, essential oils, oleoresins, terpenes, terpene-free fractions, distillates, residues, etc., obtained from Polygala paucifolia, Polygalaceae.
Details
309-990-1
101896-31-5
Details
213-813-2
1019-45-0
C13H18N2O
Details
213-814-8
1019-52-9
C7H4N2O7
Details
233-459-2
10190-55-3
MoO4Pb
Details
233-460-8
10190-66-6
C12H12N4O3S.Na
Details
233-461-3
10190-68-8
C25H22N4O9S3.2Na
Details
233-462-9
10190-69-9
C31H23N5O5S3.Na
Details
233-463-4
10190-99-5
C17H11NO7.Na
Details
233-465-5
10191-18-1
C6H15NO5S
Details
233-466-0
10191-41-0
C29H50O2
Details
233-467-6
10191-60-3
C4H6N2S2
Details
233-468-1
10192-29-7
ClHO3.H3N
Details
233-469-7
10192-30-0
H3N.H2O3S
Details
233-470-2
10192-32-2
C24H48
Details
233-471-8
10192-46-8
BH3O3.3/2Zn
Details
233-472-3
10192-62-8
C19H20O4
Details
233-473-9
10192-85-5
C3H4O2.K
Details
233-474-4
10192-93-5
C20H26
Details
233-476-5
10193-26-7
C12H12O3
Details
233-477-0
10193-36-9
H4O4Si
Details
233-478-6
10193-62-1
C14H10N6
Details
233-479-1
10193-95-0
C8H14O4S2
Details
233-480-7
10193-96-1
C12H20O6S3
Details
233-481-2
10193-98-3
C11H18O6S3
Details
233-482-8
10193-99-4
C13H20O8S4
Details
233-483-3
10194-00-0
C10H18O4S2
Details
309-991-7
101940-06-1
Details
309-992-2
101940-07-2
Details
309-993-8
101940-08-3
Details
309-994-3
101940-09-4
Details
309-995-9
101940-10-7
Details
309-996-4
101940-11-8
Details
309-998-5
101940-12-9
Details
309-999-0
101940-13-0
Details
SIF7E; VPS 8271
435-230-4
101947-16-4
SIF7E; VPS 8271
Details
233-484-9
10196-04-0
H3N.1/2H2O3S
Details
233-485-4
10196-13-1
C22H22N4O4
Details
233-487-5
10196-49-3
C6H15NOSi
Details
233-488-0
10196-66-4
C14H28O2.1/2Ba
Details
233-489-6
10196-67-5
C14H28O2.1/2Cd
Details
233-490-1
10196-68-6
C11H14O2.1/2Ba
Details
233-491-7
10196-69-7
C18H36O2.1/2Sr
Details
233-492-2
10196-75-5
C9H18N2O
Details
233-493-8
10197-71-4
C8H6O4.xNa
Details
233-494-3
10198-23-9
C12H20O2
Details
233-495-9
10199-34-5
C36H30Cl2P2Pt
Details
233-496-4
10199-89-0
C6H2ClN3O3
Details
202-996-4
102-01-2
C10H11NO2
Details
202-998-5
102-02-3
C8H11N5
Details
202-999-0
102-03-4
C9H10N2O2
Details
203-000-0
102-04-5
C15H14O
Details
203-001-6
102-05-6
C15H17N
Details
203-002-1
102-06-7
C13H13N3
Details
203-003-7
102-07-8
C13H12N2O
Details
203-004-2
102-08-9
C13H12N2S
Details
203-005-8
102-09-0
C13H10O3
Details
203-006-3
102-11-4
C11H18N2
Details
203-007-9
102-13-6
C12H16O2
Details
203-008-4
102-16-9
C15H14O2
Details
203-010-5
102-17-0
C16H16O3
Details
203-011-0
102-18-1
C18H24N2
Details
203-012-6
102-19-2
C13H18O2
Details
203-013-1
102-20-5
C16H16O2
Details
203-014-7
102-22-7
C18H24O2
Details
203-015-2
102-23-8
C12H11N3O3S
Details
203-016-8
102-24-9
C3H9B3O6
Details
203-017-3
102-25-0
C12H18
Details
203-018-9
102-26-1
C9H21N3
Details
203-019-4
102-27-2
C9H13N
Details
203-021-5
102-28-3
C8H10N2O
Details
203-022-0
102-29-4
C8H8O3
Details
203-023-6
102-30-7
C21H36Cl2N.Cl
Details
203-024-1
102-32-9
C8H8O4
Details
203-025-7
102-33-0
C8H10N2O2
Details
203-026-2
102-36-3
C7H3Cl2NO
Details
203-027-8
102-39-6
C10H10O6
Details
203-028-3
102-40-9
C10H14O4
Details
203-029-9
102-41-0
C9H13NO
Details
203-030-4
102-42-1
C8H11NO3S
Details

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