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Merck
CN

34958

1-氯丁烷

suitable for HPLC, ≥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:
41116105
NACRES:
NA.04
PubChem Substance ID:
EC Number:
203-696-6
Beilstein/REAXYS Number:
1730909
MDL number:
Assay:
≥99.8%
Grade:
HPLC grade
Technique(s):
HPLC: suitable
Bp:
77-78 °C (lit.)
Vapor pressure:
80.1 mmHg ( 78.4 °C)
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产品名称

1-氯丁烷, suitable for HPLC, ≥99.8%

InChI

1S/C4H9Cl/c1-2-3-4-5/h2-4H2,1H3

InChI key

VFWCMGCRMGJXDK-UHFFFAOYSA-N

SMILES string

CCCCCl

grade

HPLC 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 %

technique(s)

HPLC: suitable

impurities

≤0.0002% free alkali (as NH3)
≤0.001% free acid (as HCl)
≤0.001% non-volatile matter
≤0.01% water (Karl Fischer)

transmittance

230 nm, ≥65%
240 nm, ≥95%
250 nm, ≥98%

refractive index

n20/D 1.402 (lit.)

bp

77-78 °C (lit.)

mp

−123 °C (lit.)

density

0.886 g/mL at 25 °C (lit.)

application(s)

food and beverages

Quality Level

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Application

1-氯丁烷可用于合成离子液体 1-丁基-3-甲基咪唑硫酸氢盐 ([Bmim]+[HSO4]-) 和 1-丁基-3-甲基咪唑磷酸二氢盐 ([Bmim]+[H2PO4]-)。

General description

1-氯丁烷是一种卤代烷烃。它与纳米晶 MgO 在 200-350℃ 下通过脱氯化氢反应得到丁烷异构体和 MgCl 2

Other Notes

发现适用于高效液相色谱液相色谱-质谱分析的理想试剂

Packaging

溶剂用M瓶(M-Bottle for Solvents)
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pictograms

FlameHealth hazard

signalword

Danger

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

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Mannich reaction using acidic ionic liquids as catalysts and solvents.
Zhao G, et al.
Green Chemistry, 6(2), 75-77 (2004)
Changes in texture and catalytic activity of nanocrystalline MgO during its transformation to MgCl2 in the reaction with 1-chlorobutane.
Fenelonov VB, et al.
The Journal of Physical Chemistry B, 105(18), 3937-3941 (2001)
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

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