D70007
2,5-Dichlorophenol
98%
Sign Into View Organizational & Contract Pricing
Select a Size
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
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
Looking for similar products? Visit Product Comparison Guide
Signal Word
Warning
Hazard Statements
Precautionary 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
Regulatory Information
危险化学品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Effects of occupational exposure to 1,4-dichlorobenzene on hematologic, kidney, and liver functions.
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
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
R H Hill et al.
Archives of environmental health, 50(4), 277-280 (1995-07-01)
p-Dichlorobenzene is used widely in the United States as a room deodorizer, a moth repellent, and a precursor for a polymer. In a previous study of selected children in Arkansas, we found that 96% of the children had detectable urinary
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service