125903
1,3-Dibromopropane
ReagentPlus®, 99%
Synonym(s):
Trimethylene dibromide
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
Linear Formula:
Br(CH2)3Br
CAS Number:
Molecular Weight:
201.89
Beilstein:
635662
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21
Recommended Products
vapor density
7 (vs air)
Quality Level
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.)
SMILES string
BrCCCBr
InChI
1S/C3H6Br2/c4-2-1-3-5/h1-3H2
InChI key
VEFLKXRACNJHOV-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Related Categories
General description
1,3-Dibromopropane is a dihalogenated propane. It undergoes reduction catalyzed by electrogenerated solution-phase nickel(I) salen and nickel(I) salen confined in a polymer film on the surface of a carbon electrode to afford cyclopropane and propylene, respectively.
Application
1,3-Dibromopropane may be used in the preparation of chiral geminal dicationic ionic liquid and 1,3-bis(1-7′-chloro-4-quinolyl-4- piperazinyl)propane.3
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Flam. Liq. 3 - Skin Irrit. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point(F)
129.2 °F - closed cup
Flash Point(C)
54 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service