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 complex combination of hydrocarbons obtained from a benzene recovery unit. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65°C to 230°C (149°F to 446°F). This stream may contain 3 vol. % or more benzene.
272-889-5
68919-15-3
The complex combination of hydrocarbons obtained from a benzene recovery unit. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65°C to 230°C (149°F to 446°F). This stream may contain 3 vol. % or more benzene.
Details
The complex combination of hydrocarbons obtained by the thermal decomposition (at 399°C (750°F) or higher) of kerogen. It consists of hydrocarbons and heterocyclic compounds containing nitrogen, sulfur or oxygen.
269-646-0
68308-34-9
The complex combination of hydrocarbons obtained by the thermal decomposition (at 399°C (750°F) or higher) of kerogen. It consists of hydrocarbons and heterocyclic compounds containing nitrogen, sulfur or oxygen.
Details
The complex combination of hydrocarbons obtained by the pyrolysis fractionation at 816°C (1500°F) of naphtha and raffinate. It consists predominantly of hydrocarbons having a carbon number of C9 and boiling at approximately 204°C (400°F).
270-344-6
68425-29-6
The complex combination of hydrocarbons obtained by the pyrolysis fractionation at 816°C (1500°F) of naphtha and raffinate. It consists predominantly of hydrocarbons having a carbon number of C9 and boiling at approximately 204°C (400°F).
Details
The complex combination of hydrocarbons obtained by the hydroformylation of ethylene and propylene. Contains alcohols, esters, ethers, acetals, ketones, aldehydes and hydrocarbons.
273-553-0
68989-33-3
The complex combination of hydrocarbons obtained by the hydroformylation of ethylene and propylene. Contains alcohols, esters, ethers, acetals, ketones, aldehydes and hydrocarbons.
Details
The complex combination of hydrocarbons obtained by the hydration of ethylene. It contains primarily alcohols, aldehydes and ethers.
273-502-2
68987-66-6
The complex combination of hydrocarbons obtained by the hydration of ethylene. It contains primarily alcohols, aldehydes and ethers.
Details
The complex combination of hydrocarbons obtained by the fractionation of reaction products of diethylene glycol and ammonia. It may contain such compounds as bis(2-aminoethyl) ether, (methoxyethyl)morpholine, 2-(2-aminoethoxy)ethanol, and (aminoethyl)morpholine.
272-711-6
68909-76-2
The complex combination of hydrocarbons obtained by the fractionation of reaction products of diethylene glycol and ammonia. It may contain such compounds as bis(2-aminoethyl) ether, (methoxyethyl)morpholine, 2-(2-aminoethoxy)ethanol, and (aminoethyl)morpholine.
Details
The complex combination of hydrocarbons obtained by the dehydrogenation and extractive distillation of an isoamylene feed. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C8.
273-303-0
68956-47-8
The complex combination of hydrocarbons obtained by the dehydrogenation and extractive distillation of an isoamylene feed. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C8.
Details
The complex combination of hydrocarbons obtained by the dealkylation of toluene. It consists primarily of benzene and toluene with various small amounts of aromatic hydrocarbons having carbon numbers predominantly greater than C8.
273-225-7
68953-80-0
The complex combination of hydrocarbons obtained by the dealkylation of toluene. It consists primarily of benzene and toluene with various small amounts of aromatic hydrocarbons having carbon numbers predominantly greater than C8.
Details
The complex combination of hydrocarbons obtained by the catalytic alkylation of benzene with propylene. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C6 and boiling in the range of approximately -40°C to 70°C (-40°F to 158°F). This stream may contain 1 to 20 vol. % of benzene.
272-890-0
68919-16-4
The complex combination of hydrocarbons obtained by the catalytic alkylation of benzene with propylene. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C6 and boiling in the range of approximately -40°C to 70°C (-40°F to 158°F). This stream may contain 1 to 20 vol. % of benzene.
Details
The complex combination of hydrocarbons obtained by the catalytic alkylation of benzene with propylene. It consists of hydrocarbons having carbon numbers predominantly in the range of C12 through C20 and boiling in the range of approximately 250°C to 350°C (482°F to 662°F).
272-891-6
68919-17-5
The complex combination of hydrocarbons obtained by the catalytic alkylation of benzene with propylene. It consists of hydrocarbons having carbon numbers predominantly in the range of C12 through C20 and boiling in the range of approximately 250°C to 350°C (482°F to 662°F).
Details
The complex combination of hydrocarbons obtained by the aldol condensation of C4 aldehydes. It consists primarily of alcohols, esters, ethers, ketones, aldehydes and hydrocarbons.
273-585-5
68990-21-6
The complex combination of hydrocarbons obtained by the aldol condensation of C4 aldehydes. It consists primarily of alcohols, esters, ethers, ketones, aldehydes and hydrocarbons.
Details
The complex combination of hydrocarbons obtained by the acid isomerization of linalool. It consists primarily of monoterpenes, terpene alcohols and oxygenated cyclic compounds.
277-225-8
73018-51-6
The complex combination of hydrocarbons obtained by the acid isomerization of linalool. It consists primarily of monoterpenes, terpene alcohols and oxygenated cyclic compounds.
Details
The complex combination of hydrocarbons obtained as a raffinate from a Lurgi separation unit. It consists predominantly of non-aromatic hydrocarbons with various small amounts of aromatic hydrocarbons having carbon numbers predominantly in the range of C6 through C8.
270-349-3
68425-35-4
The complex combination of hydrocarbons obtained as a raffinate from a Lurgi separation unit. It consists predominantly of non-aromatic hydrocarbons with various small amounts of aromatic hydrocarbons having carbon numbers predominantly in the range of C6 through C8.
Details
The complex combination of hydrocarbons from the distillation of the products from the thermal cracking of ethane and propane. This lower boiling fraction consists predominantly of C5-C7 aromatic hydrocarbons with some unsaturated aliphatic hydrocarbons having a carbon number predominantly of C5. This stream may contain benzene.
267-565-5
67891-80-9
The complex combination of hydrocarbons from the distillation of the products from the thermal cracking of ethane and propane. This lower boiling fraction consists predominantly of C5-C7 aromatic hydrocarbons with some unsaturated aliphatic hydrocarbons having a carbon number predominantly of C5. This stream may contain benzene.
Details
The complex combination of hydrocarbons from the distillation of the products from the thermal cracking of ethane and propane. This higher boiling fraction consists predominantly of C5-C7 aromatic hydrocarbons with some unsaturated aliphatic hydrocarbons having carbon number predominantly of C5. This stream may contain benzene.
267-563-4
67891-79-6
The complex combination of hydrocarbons from the distillation of the products from the thermal cracking of ethane and propane. This higher boiling fraction consists predominantly of C5-C7 aromatic hydrocarbons with some unsaturated aliphatic hydrocarbons having carbon number predominantly of C5. This stream may contain benzene.
Details
The complex combination of hydrocarbons from the distillation of the products from catalytic cracked distillates and catalytic cracked naphtha. It consists predominantly of hydrocarbons having carbon numbers in the range of C1 through C4.
269-617-2
68307-98-2
The complex combination of hydrocarbons from the distillation of the products from catalytic cracked distillates and catalytic cracked naphtha. It consists predominantly of hydrocarbons having carbon numbers in the range of C1 through C4.
Details
The complex combination of hydrocarbons from the distillation of catalytic reformer fractionator residue. It boils approximately below 288°C (550°F).
270-722-0
68477-31-6
The complex combination of hydrocarbons from the distillation of catalytic reformer fractionator residue. It boils approximately below 288°C (550°F).
Details
The complex combination of dry gases from a gas concentration unit. It consists of hydrogen, hydrogen sulfide and hydrocarbons having carbon numbers predominantly in the range of C1 through C3.
270-774-4
68477-92-9
The complex combination of dry gases from a gas concentration unit. It consists of hydrogen, hydrogen sulfide and hydrocarbons having carbon numbers predominantly in the range of C1 through C3.
Details
The complex combination of diglycerides of fatty acids linked to the choline ester of phosphoric acid.
232-307-2
8002-43-5
The complex combination of diglycerides of fatty acids linked to the choline ester of phosphoric acid.
Details
The complex combination of alkanolamines from the distillation of reaction products of ammonia and oxirane. It consists predominantly of triethanolamine, diethanolamine and higher amines from the reaction of triethanolamine and oxirane.
273-224-1
68953-70-8
The complex combination of alkanolamines from the distillation of reaction products of ammonia and oxirane. It consists predominantly of triethanolamine, diethanolamine and higher amines from the reaction of triethanolamine and oxirane.
Details
The complex combination obtained from the depentanizer stabilization of hydrotreated kerosine. It consists primarily of hydrogen, methane, ethane, and propane with various small amounts of nitrogen, hydrogen sulfide, carbon monoxide and hydrocarbons having carbon numbers predominantly in the range of C4 through C5.
272-775-5
68911-58-0
The complex combination obtained from the depentanizer stabilization of hydrotreated kerosine. It consists primarily of hydrogen, methane, ethane, and propane with various small amounts of nitrogen, hydrogen sulfide, carbon monoxide and hydrocarbons having carbon numbers predominantly in the range of C4 through C5.
Details
The complex combination obtained by the reaction of acetaldehyde with formaldehyde. Contains pentaerythritol oligomers and their acetals, formals, hemiacetals and hemiformals.
270-480-6
68442-60-4
The complex combination obtained by the reaction of acetaldehyde with formaldehyde. Contains pentaerythritol oligomers and their acetals, formals, hemiacetals and hemiformals.
Details
The complex combination obtained by boiling the vegetable oil deodorizer distillate with mineral acid and optionally, further separating the oil phase from the aqueous phase.
273-216-8
68953-54-8
The complex combination obtained by boiling the vegetable oil deodorizer distillate with mineral acid and optionally, further separating the oil phase from the aqueous phase.
Details
The complex combination consisting primarily of phosphatides, neutral oil and water obtained by hydration of soybean oil with water, salt solutions, or dilute acids followed by recovery of precipitated gum.
272-212-3
68783-89-1
The complex combination consisting primarily of phosphatides, neutral oil and water obtained by hydration of soybean oil with water, salt solutions, or dilute acids followed by recovery of precipitated gum.
Details
The combination primarily 1,6-hexanediol and 1,5-pentanediol obtained by hydrogenolysis of mixed esters in the production of 1,6-hexanediol and boiling in the range of 200°C to 245°C (392°F to 473°F).
273-164-6
68952-17-0
The combination primarily 1,6-hexanediol and 1,5-pentanediol obtained by hydrogenolysis of mixed esters in the production of 1,6-hexanediol and boiling in the range of 200°C to 245°C (392°F to 473°F).
Details
The combination of wastes formed by the coking of bituminous coal tar pitch. It consists predominantly of carbon.
295-549-8
92062-34-5
The combination of wastes formed by the coking of bituminous coal tar pitch. It consists predominantly of carbon.
Details
The combination of phenols extracted, using isobutyl acetate, from the ammonia liquor condensed from the gas evolved in low-temperature (less than 700°C (1292°F)) destructive distillation of coal. It consists predominantly of a mixture of monohydric and dihydric phenols.
284-881-9
84988-93-2
The combination of phenols extracted, using isobutyl acetate, from the ammonia liquor condensed from the gas evolved in low-temperature (less than 700°C (1292°F)) destructive distillation of coal. It consists predominantly of a mixture of monohydric and dihydric phenols.
Details
The char resulting from processing coal in a closed reactor using an exothermic reaction and controlling the feed and air supply. Composed primarily of carbon. May contain varying amounts of ash, sulfur, volatile material and moisture.
270-070-7
68409-95-0
The char resulting from processing coal in a closed reactor using an exothermic reaction and controlling the feed and air supply. Composed primarily of carbon. May contain varying amounts of ash, sulfur, volatile material and moisture.
Details
The cellular carbonaceous mass resulting from the high temperature (greater than 700°C (1292°F)) destructive distillation of coal. Composed primarily of carbon. May contain varying amounts of sulfur and ash.
266-010-4
65996-77-2
The cellular carbonaceous mass resulting from the high temperature (greater than 700°C (1292°F)) destructive distillation of coal. Composed primarily of carbon. May contain varying amounts of sulfur and ash.
Details
The carbon-containing residue from the low-temperature carbonization coking of pitch from high-temperature coal tar. Consists primarily of carbon. Also contains small amounts of sulfur and ash.
310-274-6
140413-61-2
The carbon-containing residue from the low-temperature carbonization coking of pitch from high-temperature coal tar. Consists primarily of carbon. Also contains small amounts of sulfur and ash.
Details
The carbon containing residue from the mutual coking of coal and pitch at high temperature (above 700°C or 1272°F). Consists chiefly of carbon, can also contain heteroatoms and ash.
310-222-2
140203-13-0
The carbon containing residue from the mutual coking of coal and pitch at high temperature (above 700°C or 1272°F). Consists chiefly of carbon, can also contain heteroatoms and ash.
Details
The carbon containing residue from the carbonization coking of pitch from high temperature (>700°C or >1272°F) coal tar. Consists primarily of carbon. Also contains small amounts of sulfur and ash.
310-221-7
140203-12-9
The carbon containing residue from the carbonization coking of pitch from high temperature (>700°C or >1272°F) coal tar. Consists primarily of carbon. Also contains small amounts of sulfur and ash.
Details
The by-product from the destructive distillation of coal. Almost black semisolid. A complex combination of aromatic hydrocarbons, phenolic compounds, nitrogen bases and thiophene.
232-361-7
8007-45-2
The by-product from the destructive distillation of coal. Almost black semisolid. A complex combination of aromatic hydrocarbons, phenolic compounds, nitrogen bases and thiophene.
Details
The brown polymeric product from the decomposition of organic matter, particularly dead plants. This combination of polymers may contain aromatic and heterocyclic structures, carboxy groups, and nitrogen.
215-809-6
1415-93-6
The brown polymeric product from the decomposition of organic matter, particularly dead plants. This combination of polymers may contain aromatic and heterocyclic structures, carboxy groups, and nitrogen.
Details
The bottoms from fractionation boiling approximately above 360°C (680°F).
271-073-6
68515-32-2
The bottoms from fractionation boiling approximately above 360°C (680°F).
Details
The barium salt of the substance is identified in the Colour Index by Colour Index Constitution Number, C.I. 50420.
270-933-8
68510-98-5
The barium salt of the substance is identified in the Colour Index by Colour Index Constitution Number, C.I. 50420.
Details
The aqueous solution resulting from the reaction of lignocellulosic substances (wood or other agricultural fiber sources) with one or more pulping chemicals including those used in the kraft, sulfite, semichemical or other pulping processes. Composition is highly variable and includes excess pulping chemicals, dissolved and degraded cellulose, hemicellulose and lignin.
266-111-3
66071-92-9
The aqueous solution resulting from the reaction of lignocellulosic substances (wood or other agricultural fiber sources) with one or more pulping chemicals including those used in the kraft, sulfite, semichemical or other pulping processes. Composition is highly variable and includes excess pulping chemicals, dissolved and degraded cellulose, hemicellulose and lignin.
Details
The aqueous solution obtained by the distillation and extraction of oxidized alkaline lignin liquor.
271-021-2
68514-06-7
The aqueous solution obtained by the distillation and extraction of oxidized alkaline lignin liquor.
Details
The aqueous slurry produced when anthracene is contacted with water in a cooling tower. It consists primarily of anthracene.
270-058-1
68409-72-3
The aqueous slurry produced when anthracene is contacted with water in a cooling tower. It consists primarily of anthracene.
Details
The aqueous liquor produced during the desulfurization of coke-oven gas by the Stretford process (high temperature destructive distillation). Consists primarily of an alkaline solution of sodium thiocyanate and sodium thiosulfate with traces of vanadium and suspended sulfur.
293-802-7
91082-87-0
The aqueous liquor produced during the desulfurization of coke-oven gas by the Stretford process (high temperature destructive distillation). Consists primarily of an alkaline solution of sodium thiocyanate and sodium thiosulfate with traces of vanadium and suspended sulfur.
Details
The aqueous layer formed by the acidulation of vegetable-oil soap during the production of vegetable-oil. Composed primarily of sodium sulfate with minor amounts of vegetable-oil and neutral materials of vegetable origins.
272-793-3
68911-90-0
The aqueous layer formed by the acidulation of vegetable-oil soap during the production of vegetable-oil. Composed primarily of sodium sulfate with minor amounts of vegetable-oil and neutral materials of vegetable origins.
Details
The aqueous layer formed by acidulation of tall-oil soap with sulfuric acid during the production of tall oil. Composed primarily of a solution of sodium sulfate, the remaining being lignin and tall oil.
266-038-7
65997-02-6
The aqueous layer formed by acidulation of tall-oil soap with sulfuric acid during the production of tall oil. Composed primarily of a solution of sodium sulfate, the remaining being lignin and tall oil.
Details
The aqueous extract produced by an acidic wash of alkali-washed napthalene oil. Composed primarily of acid salts of various aromatic nitrogen bases including pyridine, quinoline and their alkyl derivatives.
292-623-1
90641-00-2
The aqueous extract produced by an acidic wash of alkali-washed napthalene oil. Composed primarily of acid salts of various aromatic nitrogen bases including pyridine, quinoline and their alkyl derivatives.
Details
The aqueous extract produced by an acidic wash of alkali-washed carbolic oil. Composed primarily of acid salts of various aromatic nitrogen bases including pyridine, quinoline and their alkyl derivatives.
292-622-6
90640-99-6
The aqueous extract produced by an acidic wash of alkali-washed carbolic oil. Composed primarily of acid salts of various aromatic nitrogen bases including pyridine, quinoline and their alkyl derivatives.
Details
The aqueous extract from naphthalene oil produced by an alkaline wash such as aqueous sodium hydroxide. Composed primarily of the alkali salts of various phenolic compounds.
292-611-6
90640-89-4
The aqueous extract from naphthalene oil produced by an alkaline wash such as aqueous sodium hydroxide. Composed primarily of the alkali salts of various phenolic compounds.
Details
The aqueous extract from carbolic oil produced by an alkaline wash such as aqueous sodium hydroxide. Composed primarily of the alkali salts of various phenolic compounds.
292-610-0
90640-88-3
The aqueous extract from carbolic oil produced by an alkaline wash such as aqueous sodium hydroxide. Composed primarily of the alkali salts of various phenolic compounds.
Details
The aqueous extract from alkali-washed low-temperature coal tar middle oil produced by an acidic wash, such as aqueous sulfuric acid. An aqueous solution containing primarily the acid salts of various aromatic nitrogen bases.
310-295-0
141785-67-3
The aqueous extract from alkali-washed low-temperature coal tar middle oil produced by an acidic wash, such as aqueous sulfuric acid. An aqueous solution containing primarily the acid salts of various aromatic nitrogen bases.
Details
The anthracene-rich solid obtained by the crystallization and centrifuging of anthracene oil. It is composed primarily of anthracene, carbazole and phenanthrene.
292-603-2
90640-81-6
The anthracene-rich solid obtained by the crystallization and centrifuging of anthracene oil. It is composed primarily of anthracene, carbazole and phenanthrene.
Details
The anthracene oil fraction obtained from the fractional distillation of high temperature coal tar is debased using sulfuric acid, and subsequently neutralized with aqueous ammonia to obtain free bases. Contains chiefly acridine, carbazole, and higher boiling bases. It distills in the range 325°C to 365°C (619°F to 689°F).
310-242-1
140203-31-2
The anthracene oil fraction obtained from the fractional distillation of high temperature coal tar is debased using sulfuric acid, and subsequently neutralized with aqueous ammonia to obtain free bases. Contains chiefly acridine, carbazole, and higher boiling bases. It distills in the range 325°C to 365°C (619°F to 689°F).
Details
The alcoholic solution of macerated Vanilla planifolia.
232-463-1
8047-24-3
The alcoholic solution of macerated Vanilla planifolia.
Details
The acqueous extract from creosote oil produced by an acidic wash such as aqueous sulfuric acid. Composed primarily of acid salts of quinoline and isoquinoline.
310-212-8
91995-30-1
The acqueous extract from creosote oil produced by an acidic wash such as aqueous sulfuric acid. Composed primarily of acid salts of quinoline and isoquinoline.
Details
447-000-0
-
THBP
Details
THANCAT AN 20
407-360-1
116230-20-7
THANCAT AN 20
Details
THANCAT AN 10
404-810-9
4524-95-2
THANCAT AN 10
Details
431-120-5
-
TGBMA MONOMER
Details
TG-SA
411-570-9
41481-66-7
TG-SA
Details
453-520-9
-
TFXOH
Details
458-390-7
6226-25-1
TFOL-TF
Details
435-890-3
652-18-6
TFBA
Details
TFA-4713
418-960-8
-
TFA-4713
Details
TFA LYS-PRO TOSYLATE; TFA LYSYL PROLINE PARA-TOLUENE SULPHONATE
402-160-0
-
TFA LYS-PRO TOSYLATE; TFA LYSYL PROLINE PARA-TOLUENE SULPHONATE
Details
453-420-5
-
TETT
Details
TETRAMYL
421-930-7
-
TETRAMYL
Details
TETRAMMINE PALLADIUM SULFATE
426-980-3
13601-06-4
TETRAMMINE PALLADIUM SULFATE
Details
TETRAFLUOROQUINOLONE
406-710-0
-
TETRAFLUOROQUINOLONE
Details
TETRACONAZOLE
407-760-6
112281-77-3
TETRACONAZOLE
Details
TETRACHLOROTEREPHTHALONITRILE
401-550-8
1897-41-2
TETRACHLOROTEREPHTHALONITRILE
Details
449-410-5
-
TETRABENZYLCYCLEN
Details
426-730-3
123439-82-7
TETRAAMMIN-PLATIN(II)-DIHYDROGENCARBONAT; TETRAMMINE PLATINUM HYDROGEN CARBONATE; TETRAAMMINE PLATINUM (II) HYDROGEN CARBONATE
Details
425-270-0
134620-00-1
TETRAAMMIN-PALLADIUM-DIHYDROGENCARBONAT; TETRAMMINE PALLADIUM HYDROGEN CARBONATE; TETRAAMMINE PALLADIUM (II) HYDROGEN CARBONATE
Details
458-640-5
-
TETRAALLYLSILAN
Details
TERTIARYBUTYLPHOSPHINE; TERTIÄRBUTYLPHOSPHIN
423-330-0
-
TERTIARYBUTYLPHOSPHINE; TERTIÄRBUTYLPHOSPHIN
Details
TERTIARYBUTYLARSINE; TERTIÄRBUTYLARSIN
423-320-6
4262-43-5
TERTIARYBUTYLARSINE; TERTIÄRBUTYLARSIN
Details
437-440-1
-
TERT-AMYL OXALATE
Details
429-810-6
-
TERRESTRAL
Details
436-900-9
39290-90-9
TERRACESS P
Details
445-620-6
39318-30-4
TERRACESS L
Details
427-830-1
-
TERON N-718K
Details
TEPIC-H
423-400-0
59653-74-6
TEPIC-H
Details
423-030-1
-
TELEPHOTO 1
Details
447-860-7
144177-62-8
TELAM
Details
427-760-1
-
TEGUDORPHINE
Details
460-100-9
342573-75-5
TEGO IL IMES
Details
TEGO ANTIFOAM C2600
400-960-4
-
TEGO ANTIFOAM C2600
Details
459-280-1
388603-24-5
TED-15L
Details
429-390-4
-
TECHMORE VG 3101L
Details
TEBUCONAZOLE RESP. HWG 1608
403-640-2
107534-96-3
TEBUCONAZOLE RESP. HWG 1608
Details
TDEAT
437-500-7
4419-47-0
TDEAT
Details
432-830-8
-
TCPY
Details
434-220-7
-
TCPM
Details
434-390-2
-
TCPC
Details
446-820-6
-
TCO; TRICYCLIC DIHYDROQUINOLINE; TRICYCLIC OLEFIN; TRICYCLIQUE DIHYDRO QUINOLEINE; TRICYCLONE
Details
427-360-5
-
TCO 197
Details
421-300-1
138564-59-7
TCN INTERMEDIATE
Details
420-970-2
-
TCDO; TETRACHLORODEKAOXID-KOMPLEX IN WÄSSRIGER LÖSUNG
Details
418-030-1
-
TCD-DI-HEA
Details
TCD EMULGATOR
407-410-2
-
TCD EMULGATOR
Details
423-440-9
-
TBYT
Details
TBUAP
450-360-1
82560-12-1
TBUAP
Details
TBTU
423-040-4
125700-67-6
TBTU
Details

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