125903
1,3-二溴丙烷
99%, liquid, ReagentPlus®
别名:
三亚甲基二溴
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关于此项目
线性分子式:
Br(CH2)3Br
化学文摘社编号:
分子量:
201.89
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
203-690-3
MDL number:
Beilstein/REAXYS Number:
635662
产品名称
1,3-二溴丙烷, ReagentPlus®, 99%
InChI key
VEFLKXRACNJHOV-UHFFFAOYSA-N
InChI
1S/C3H6Br2/c4-2-1-3-5/h1-3H2
SMILES string
BrCCCBr
vapor density
7 (vs air)
product line
ReagentPlus®
assay
99%
form
liquid
refractive index
n20/D 1.524 (lit.)
bp
167 °C (lit.)
mp
−34 °C (lit.)
density
1.989 g/mL at 25 °C (lit.)
Quality Level
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Application
1,3-二溴丙烷可用于制备手性孪生双阳离子离子液体 和 1,3-双（1-7′-氯-4-喹啉基-4-哌嗪基）丙烷。3
General description
1,3-二溴丙烷是一种二卤代丙烷。在碳电极表面的聚合物膜中，它分别被电生液相镍 (I) 手性和镍 (I) 手性催化还原生成环丙烷和丙烯。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Flam. Liq. 3 - Skin Irrit. 2
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
129.2 °F - closed cup
flash_point_c
54 °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
Synthesis of Chiral Geminal Dicationic Ionic Liquid from Amino Acids.
Yin A, et al.
Asian Journal of Chemistry, 25(12), 6721-6721 (2013)
Catalytic reduction of α,ω-dihaloalkanes with nickel (I) salen as a homogeneous-phase and polymer-bound mediator.
Dahm CE and Peters DG.
Journal of Electroanalytical Chemistry, 406(1), 119-129 (1996)
A R Jones et al.
Xenobiotica; the fate of foreign compounds in biological systems, 11(8), 541-546 (1981-08-01)
1. The metabolism of 1,3-dibromopropane had been investigated in the rat. Two conjugated metabolites have been isolated from the urine and identified as S-(3-hydroxypropyl)cysteine and N-acetyl-S-(3-hydroxypropyl)cysteine. 2. An oxidation product, identified as beta-bromolactic acid, has been isolated as a urinary
Rasmus Y Brogaard et al.
The journal of physical chemistry. A, 112(42), 10481-10486 (2008-09-30)
We have conducted wave packet simulations of excited-state dynamics of 1,3-dibromopropane (DBP) with the aim of reproducing the experimental results of the gas-phase pump-probe experiment by Kotting et al. [ Kotting, C. ; Diau, E. W.-G. ; Sølling, T. I.
Sang Kyu Lee et al.
Journal of toxicology and environmental health. Part A, 70(15-16), 1381-1390 (2007-07-27)
To determine a possible role of glutathione (GSH) conjugation in 1,3-dibromopropane (1,3-DBP)-induced hepatotoxicity and immunotoxicity, female BALB/c mice were treated orally with 1,3-DBP. Based on the liquid chromatography/electrospray ionization-tandem mass spectrometry (LC/ESI-MS) analyses, two forms of S-bromopropyl GSH were observed
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