蒸汽密度
3.2 (vs air)
蒸汽压
80.1 mmHg ( 78.4 °C)
等级
purum
方案
≥99.0% (GC)
自燃温度
860 °F
expl. lim.
10.1 %
杂质
≤1% benzene
折射率
n20/D 1.402 (lit.)
n20/D 1.402
沸点
77-78 °C (lit.)
mp
−123 °C (lit.)
密度
0.886 g/mL at 25 °C (lit.)
SMILES字符串
CCCCCl
InChI
1S/C4H9Cl/c1-2-3-4-5/h2-4H2,1H3
InChI key
VFWCMGCRMGJXDK-UHFFFAOYSA-N
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Danger
危险声明
危险分类
Aquatic Chronic 3 - Asp. Tox. 1 - Flam. Liq. 2
储存分类代码
3 - Flammable liquids
WGK
WGK 2
闪点(°F)
10.4 °F - closed cup
闪点(°C)
-12 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
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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).
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.
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
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
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
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