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D70007

Sigma-Aldrich

2,5-Dichlorophenol

98%

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About This Item

Linear Formula:
Cl2C6H3OH
CAS Number:
Molecular Weight:
163.00
Beilstein:
1907692
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Pricing and availability is not currently available.

Assay

98%

form

chunks
powder or crystals

bp

211 °C (lit.)

mp

54-57 °C (lit.)

SMILES string

Oc1cc(Cl)ccc1Cl

InChI

1S/C6H4Cl2O/c7-4-1-2-5(8)6(9)3-4/h1-3,9H

InChI key

RANCECPPZPIPNO-UHFFFAOYSA-N

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Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 2

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Pao-Kuei Hsiao et al.
International archives of occupational and environmental health, 82(9), 1077-1085 (2009-02-28)
To investigate the effects of 1,4-dichlorobenzene (1,4-DCB) on kidney, liver, and hematological functions of workers in insect repellent factories in Taiwan. A cross-sectional study was performed comparing 46 exposed workers and 29 non-exposed workers. Health information was collected using questionnaires
J C Spain et al.
Applied and environmental microbiology, 55(10), 2648-2652 (1989-10-01)
Pseudomonas putida F1 contains a multicomponent enzyme system, toluene dioxygenase, that converts toluene and a variety of substituted benzenes to cis-dihydrodiols by the addition of one molecule of molecular oxygen. Toluene-grown cells of P. putida F1 also catalyze the monohydroxylation
K Tegethoff et al.
Mutation research, 470(2), 161-167 (2000-10-12)
The genotoxic potential of 1,4-dichlorobenzene (1,4-DCB) has been extensively evaluated in vitro and in vivo. The majority of the studies demonstrated the absence of a genotoxic potential for 1, 4-DCB. At variance are a bone marrow micronucleus test (MNT) after
N Díaz-Alejo et al.
Journal of chromatography, 622(2), 179-186 (1993-12-22)
O-Hexyl O-2,5-dichlorophenyl phosphoramidate (HDCP) is a chiral organophosphorus compound that undergoes enzymatic hydrolysis in the rat and hen. Studies of the stereospecificity of its biodegradation are necessary to establish HDCP toxicity. To this effect, methods have been developed for the
Xiaoyun Ye et al.
Environment international, 35(8), 1160-1163 (2009-08-12)
In humans, the metabolism of environmental phenols may include the formation of conjugated species (e.g., glucuronides and sulfates), but the free species-not the conjugated forms-are considered biologically active. Therefore, information on the concentration of these free species in blood or

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