09651
1-氯丁烷
biotech. grade, ≥99.8%
别名:
丁基氯
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关于此项目
线性分子式:
CH3(CH2)3Cl
化学文摘社编号:
分子量:
92.57
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-696-6
Beilstein/REAXYS Number:
1730909
MDL number:
Assay:
≥99.8%
Form:
liquid
产品名称
1-氯丁烷, biotech. grade, ≥99.8%
InChI key
VFWCMGCRMGJXDK-UHFFFAOYSA-N
InChI
1S/C4H9Cl/c1-2-3-4-5/h2-4H2,1H3
SMILES string
CCCCCl
grade
biotech. grade
vapor density
3.2 (vs air)
vapor pressure
80.1 mmHg ( 78.4 °C)
assay
≥99.8%
form
liquid
autoignition temp.
860 °F
expl. lim.
10.1 %
impurities
≤0.01% water (Karl Fischer)
evapn. residue
≤0.0003%
refractive index
n20/D 1.402 (lit.)
n20/D 1.402
bp
77-78 °C (lit.)
mp
−123 °C (lit.)
density
0.886 g/mL at 25 °C (lit.)
suitability
corresponds for Infrared spectrum
in accordance for sequence analysis test
functional group
alkyl halide
chloro
storage temp.
2-8°C
Quality Level
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Packaging
专用 200ml 包装，可直接用于常用测序仪。
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 3 - Asp. Tox. 1 - Flam. Liq. 2
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
10.4 °F - closed cup
flash_point_c
-12 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Benjamin Erable et al.
Chemosphere, 65(7), 1146-1152 (2006-05-26)
Five bacterial strains were compared for halogenated compounds conversion in aqueous media. Depending on the strain, the optimal temperature for dehalogenase activity of resting cells varied from 30 to 45 degrees C, while optimal pH raised from 8.4 to 9.0.
M E Alburges et al.
Journal of analytical toxicology, 19(6), 381-386 (1995-10-01)
Ibogaine, an indolamine derivative, is currently being investigated as a potential agent in the treatment of stimulant and opiate addiction. We developed a rapid, sensitive, and specific method for the analysis of ibogaine and its putative active metabolite, 12-hydroxy-ibogamine (12-OH-ibogamine).
D B Janssen et al.
Applied and environmental microbiology, 53(3), 561-566 (1987-03-01)
A 1,6-dichlorohexane-degrading strain of Acinetobacter sp. was isolated from activated sludge. The organism could grow with and quantitatively release halide from 1,6-dichlorohexane, 1,9-dichlorononane, 1-chloropentane, 1-chlorobutane, 1-bromopentane, ethylbromide, and 1-iodopropane. Crude extracts contained an inducible novel dehalogenase that liberated halide from
C Chebli et al.
Pharmaceutical research, 16(9), 1436-1440 (1999-09-25)
Amylose derivatives form an important group of polymers, and many of them can be used as drug sustained-release systems. Substituted amylose can be prepared in a 1-step reaction with substituent(s) in a basic medium. The substituents can be represented as
T Yokota et al.
Journal of bacteriology, 169(9), 4049-4054 (1987-09-01)
A haloalkane dehalogenase was purified to electrophoretic homogeneity from cell extracts of a 1-chlorobutane-utilizing strain, m15-3, which was identified as a Corynebacterium sp. The enzyme hydrolyzed C2 to C12 mono- and dihalogenated alkanes, some haloalcohols, and haloacids. The Km value
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