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Supelco

2,3,5-Trichlorophenol

analytical standard

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About This Item

Empirical Formula (Hill Notation):
C6H3Cl3O
CAS Number:
Molecular Weight:
197.45
Beilstein/REAXYS Number:
2046862
EC Number:
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:

grade

analytical standard

CofA

current certificate can be downloaded

packaging

ampule of 100 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

environmental

format

neat

storage temp.

2-30°C

SMILES string

Oc1cc(Cl)cc(Cl)c1Cl

InChI

1S/C6H3Cl3O/c7-3-1-4(8)6(9)5(10)2-3/h1-2,10H

InChI key

WWGQHTJIFOQAOC-UHFFFAOYSA-N

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General description

2,3,5-Trichlorophenol belongs to the class of substituted phenol compounds. They are widely used in industrial applications such as synthesis of pesticides, dyes, drugs, plastics, etc. They are found in the environment as pollutant due to their extensive usage.

Application

2,3,5-Trichlorophenol may be used as an analytical reference standard for the determination of the analyte in landfill leachates, aqueous samples, and environmental samples by various chromatographic techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

Exclamation markEnvironment

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Customers Also Viewed

L Drummond et al.
British journal of industrial medicine, 45(7), 493-497 (1988-07-01)
Plasma gamma-hexachlorocyclohexane (gamma-HCH) and three urinary trichlorophenols were measured in forestry workers who were engaged in planting seedlings treated with gamma-HCH. These two procedures were assessed as potential biological monitoring methods and the data were compared with reported clinical symptoms.
P T Charles et al.
Bioconjugate chemistry, 6(6), 691-694 (1995-11-01)
A synthetic scheme has been developed for the preparation of a dye-labeled analog of polychlorinated biphenyls. The reaction of 2,3,5-trichlorophenol with 3-bromopropylamine hydrobromide under basic conditions was used to introduce a free primary amine group into the parent compound by
V S Bondar et al.
FEMS microbiology letters, 181(1), 73-82 (1999-11-24)
The regiospecificity of hydroxylation of C2-halogenated phenols by Rhodococcus opacus 1G was investigated. Oxidative defluorination at the C2 position ortho with respect to the hydroxyl moiety was preferred over hydroxylation at the non-fluorinated C6 position for all 2-fluorophenol compounds studied.
Evaluation of a dedicated gas chromatography-mass spectrometry method for the analysis of phenols in water.
Vermeulen A, et al.
Journal of Chromatography A, 1071(1-2), 41-46 (2005)
Amita Limaye et al.
Toxicology letters, 179(1), 23-28 (2008-05-20)
Chlorophenols and their derivatives are a major component of environmental pollutants that are potential immunotoxicants. Deaminase assay performed on peripheral blood mononuclear cells (PBMCs) exposed to chlorophenolic compounds and its derivatives demonstrated a decreased proliferation rate and cell death. Chlorophenolic

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