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442285

Supelco

2,3,5-Trichlorophenol

analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C6H3Cl3O
Número de CAS:
933-78-8
Peso molecular:
197.45
Beilstein:
2046862
Número CE:
213-272-2
Número MDL:
MFCD00002164
Código UNSPSC:
12000000
ID de la sustancia en PubChem:
24867781

grado

analytical standard

CofA

current certificate can be downloaded

envase

ampule of 100 mg

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

environmental

Formato

neat

temp. de almacenamiento

2-30°C

cadena SMILES

Oc1cc(Cl)cc(Cl)c1Cl

InChI

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

Clave InChI

WWGQHTJIFOQAOC-UHFFFAOYSA-N

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Descripción general

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.[1]

Aplicación

2,3,5-Trichlorophenol may be used as an analytical reference standard for the determination of the analyte in landfill leachates,[2] aqueous samples,[1][3][4][5] and environmental samples[6] 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.

Pictogramas

Exclamation markEnvironment
GHS07,GHS09

Palabra de señalización

Warning

Frases de peligro

H302,H315,H319,H335,H410

Clasificaciones de peligro

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

Órganos de actuación

Respiratory system

Código de clase de almacenamiento

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

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

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

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Certificados de análisis (COA)

Lot/Batch Number
LC26367V
LC25778V
LC23868V
LC22796V
LC10565V

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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
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.
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.
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
Development and optimization of a method for the analysis of phenols and chlorophenols from aqueous samples by gas chromatography-mass spectrometry, after solid-phase extraction and trimethylsilylation.
Kovacs A, et al.
Microchemical Journal, Devoted to the Application of Microtechniques in All Branches of Science, 99(1), 125-131 (2011)
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