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Supelco

2,3,5-Trichlorophenol

analytical standard

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About This Item

Formula empirica (notazione di Hill):
C6H3Cl3O
Numero CAS:
933-78-8
Peso molecolare:
197.45
Beilstein:
2046862
Numero CE:
213-272-2
Numero MDL:
MFCD00002164
Codice UNSPSC:
12000000
ID PubChem:
24867781

Grado

analytical standard

CdA

current certificate can be downloaded

Confezionamento

ampule of 100 mg

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

environmental

Formato

neat

Temperatura di conservazione

2-30°C

Stringa SMILE

Oc1cc(Cl)cc(Cl)c1Cl

InChI

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

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Descrizione generale

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]

Applicazioni

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.

Pittogrammi

Exclamation markEnvironment
GHS07,GHS09

Avvertenze

Warning

Indicazioni di pericolo

H302,H315,H319,H335,H410

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
LC26367V
LC25778V
LC23868V
LC22796V
LC10565V

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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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