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线性分子式:
ClCH2CHClCH2OH
化学文摘社编号:
分子量:
128.99
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-470-0
Beilstein/REAXYS Number:
1732060
MDL number:
Assay:
≥97.0% (GC)
InChI key
ZXCYIJGIGSDJQQ-UHFFFAOYSA-N
InChI
1S/C3H6Cl2O/c4-1-3(5)2-6/h3,6H,1-2H2
SMILES string
OCC(Cl)CCl
assay
≥97.0% (GC)
density
1.360 g/mL at 20 °C (lit.)
functional group
chloro, hydroxyl
Quality Level
General description
2,3-Dichloro-1-propanol belongs to the group of chloropropanols. Inhibitory effects of 2,3-dichloro-1-propanol on T cell both in vivo and in vitro is reported. Improved enantioselective resolution of (R,S)-2,3-dichloro-1-propanol to (S)-2, 3-dichloro-1-propanol by whole cells of a recombinant Escherichia coli in n-heptane-aqueous biphasic system is reported.
Application
2,3-Dichloro-1-propanol may be employed as carbon and energy supplement for the growth of Pseudomonas putida strain (MC4).
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Dermal - Acute Tox. 3 Oral - Eye Irrit. 2
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
199.4 °F
flash_point_c
93 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
A J Effendi et al.
Applied and environmental microbiology, 66(7), 2882-2887 (2000-07-06)
2,3-Dichloro-1-propanol is more chemically stable than its isomer, 1, 3-dichloro-2-propanol, and is therefore more difficult to degrade. The isolation of bacteria capable of complete mineralization of 2, 3-dichloro-1-propanol was successful only from enrichments at high pH. The bacteria thus isolated
C Aguilar et al.
Journal of chromatography. A, 867(1-2), 207-218 (2000-02-12)
On-line combination of equilibrium sorptive enrichment and gas chromatography is used for the analysis of a group of pollutants varying widely in polarity and volatility in aqueous samples at trace levels. For the ESE process open-tubular traps were used. The
Jing Lu et al.
International immunopharmacology, 17(2), 321-328 (2013-07-16)
2,3-Dichloro-1-propanol (2,3-DCP) is a member of a group of chemicals known as chloropropanols. Currently, immunotoxicity of 2,3-DCP has not been reported. In the present study, we studied its inhibitory effects on T cell both in vivo and in vitro. The
A H Hammond et al.
Chemico-biological interactions, 122(2), 107-115 (1999-10-21)
The effect of aldehyde dehydrogenase inhibition by cyanamide pre-treatment in vitro on dichloropropanol-dependent toxicity and glutathione depletion was investigated in 24 h rat hepatocyte cultures. Cyanamide pre-treatment had no effect on nitrophenol hydroxylase, 7-methoxy-, 7-ethoxy- or 7-benzyloxyresorufin O-dealkylase activities in
M Koga et al.
Journal of UOEH, 14(1), 13-22 (1992-03-01)
Urinary metabolites of dichloropropanols in rats were analyzed by gas chromatography-mass spectrometry (GC/MS). Solutions of dichloropropanols consisting of 1, 3-dichloro-2-propanol (DC2P) and 2, 3-dichloro-1-propanol (DC1P) were diluted in a saline at the concentration of 100 mg/ml, and 0.1 ml of
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