545899
3,5-Dichlorocatechol
97%
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About This Item
Linear Formula:
Cl2C6H2(OH)2
CAS Number:
Molecular Weight:
179.00
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
InChI
1S/C6H4Cl2O2/c7-3-1-4(8)6(10)5(9)2-3/h1-2,9-10H
SMILES string
Oc1cc(Cl)cc(Cl)c1O
InChI key
XSXYVLIPQMXCBV-UHFFFAOYSA-N
assay
97%
mp
79.5-84.5 °C (lit.)
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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S N Gorlatov et al.
Journal of basic microbiology, 32(3), 177-184 (1992-01-01)
Effects of aromatic and nonaromatic cosubstrates on the rate of 2,4-dichlorophenol degradation by R. erythropolis 1CP were studied under growth and nongrowth conditions. Glucose and maltose were found to accelerate 2,4-dichlorophenol (initial conc. 50 mg/l) dechlorination from 11 days to
Stefan G Huber et al.
Environmental science & technology, 41(22), 7802-7806 (2007-12-14)
The formation of volatile compounds during abiotic degradation processes of aromatic compounds in soil has been the subject of many experimental studies but should be examined further. In this context, the present work investigates the natural formation of carbon suboxide
Monika Thiel et al.
Archives of microbiology, 183(2), 80-94 (2005-02-03)
The genes responsible for the degradation of 2,4-dichlorophenoxyacetate (2,4-D) by alpha-Proteobacteria have previously been difficult to detect by using gene probes or polymerase chain reaction (PCR) primers. PCR products of the chlorocatechol 1,2-dioxygenase gene, tfdC, now allowed cloning of two
S Liu et al.
Gene, 268(1-2), 207-214 (2001-05-23)
The modified-ortho pathway genes responsible for the degradation of chlorocatechols produced from 3- and 4-chlorobenzoate in Burkholderia sp. NK8 were cloned and analyzed. The five genes predicted to encode a LysR-type transcriptional regulator, chlorocatechol 1,2-dioxygenase, chloromuconate cycloisomerase, dienelactone hydrolase, and
Dirk Benndorf et al.
Proteomics, 6(11), 3319-3329 (2006-04-26)
Pseudomonas putida KT2440 is often used as a model to investigate toxicity mechanisms and adaptation to hazardous chemicals in bacteria. The objective of this paper was to test the impact of the chlorophenoxy herbicides 2,4-dichlorophenoxyacetic acid (2,4-D) and 2-(2,4-dichlorophenoxy)propanoic acid
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