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Merck
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Key Documents

235393

Sigma-Aldrich

2,4,6-Trichloroanisole

99%

Synonym(s):

2,4,6-Trichloro-1-methoxybenzene

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About This Item

Linear Formula:
Cl3C6H2OCH3
CAS Number:
Molecular Weight:
211.47
Beilstein:
2329219
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

bp

132 °C/28 mmHg (lit.)

mp

60-62 °C (lit.)

solubility

benzene: soluble(lit.)
cyclohexanone: soluble(lit.)
dioxane: soluble(lit.)
methanol: soluble(lit.)
water: insoluble (practically)(lit.)

SMILES string

COc1c(Cl)cc(Cl)cc1Cl

InChI

1S/C7H5Cl3O/c1-11-7-5(9)2-4(8)3-6(7)10/h2-3H,1H3

InChI key

WCVOGSZTONGSQY-UHFFFAOYSA-N

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General description

2,4,6-Trichloroanisole (TCA) is responsible for the cork taint in wines. TCA has been quantitated in bark cork stoppers by supercritical fluid extraction (SFE) method. Degradation of TCA catalyzed by raw bauxite via ozonation in water has been investigated.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 4 - Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Fei Qi et al.
Journal of hazardous materials, 168(1), 246-252 (2009-03-11)
A kind of inexpensive and environmental friendly mineral, the raw bauxite has been used successfully as a catalyst combined with ozonation in the degradation of 2,4,6-trichloroanisole (TCA). The catalyst was characterized by using various analytical techniques. X-ray powder diffraction (XRD)
M K Taylor et al.
Journal of agricultural and food chemistry, 48(6), 2208-2211 (2000-07-11)
2,4,6-Trichloroanisole (TCA) is the compound most often associated with cork taint in wines and has been shown to have a very low sensory threshold ( approximately 5 ng/L in wine). A supercritical fluid extraction (SFE) method for TCA in bark

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