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MilliporeSigma

140961

1,2-Dibromopropane

97%

Synonym(s):

Propylene dibromide

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100 G

$32.47

$32.47

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About This Item

Linear Formula:
CH3CHBrCH2Br
CAS Number:
Molecular Weight:
201.89
Beilstein/REAXYS Number:
1718884
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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assay

97%

form

liquid

refractive index

n20/D 1.519 (lit.)

bp

140-142 °C (lit.)

mp

−55 °C (lit.)

solubility

organic solvents: miscible
water: slightly soluble

density

1.937 g/mL at 25 °C (lit.)

SMILES string

CC(Br)CBr

InChI

1S/C3H6Br2/c1-3(5)2-4/h3H,2H2,1H3

InChI key

XFNJYAKDBJUJAJ-UHFFFAOYSA-N

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Application

Photodissociation dynamics of 1,2-dibromopropane at 234 and 265 nm has been investigated by using velocity map ion imaging method[1]. 1,2-Dibromopropane was used to study the effect of reductant concentration, reductant contact time and suspension pH on reductive dechlorination of carbon tetrachloride by soil manipulated with Fe(II) andHS-[2]. It was used as internal standard during the determination of nitrogenous disinfection byproduct trichloronitromethane by gas chromatography mass spectrometry[3].

Biochem/physiol Actions

1,2-Dibromopropane induces hepatotoxicity and immunotoxicity in female BALB/c mice[4].

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Warning

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

122.0 °F - closed cup

flash_point_c

50 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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C E Zoetemelk et al.
Drug metabolism and disposition: the biological fate of chemicals, 14(5), 601-607 (1986-09-01)
1,2-Dibromopropane was administered orally in doses of 50-350 mg/kg to male Wistar rats. Four mercapturic acids were identified in urine by GC/MS, viz. N-acetyl-S-(2-oxopropyl)-L-cysteine (I), N-acetyl-S-(2-hydroxypropyl)-L-cysteine (II), N-acetyl-S-(1-carboxyethyl)-L-cysteine (III), and N-acetyl-S-(2-bromo-2-propenyl)-L-cysteine (IV). Mercapturic acid IV was a minor metabolite which
Chun-Sheng Ding et al.
Huan jing ke xue= Huanjing kexue, 34(8), 3113-3118 (2013-11-07)
A novel method is described in this paper, which uses methyl tertiary butyl ether (MTBE) as extractant and 1,2-dibromopropane as internal standard for the determination of nitrogenous disinfection byproduct trichloronitromethane (TCNM) by gas chromatography mass spectrometry (GC-MS). The formation process
Renato Bonora et al.
Nanomaterials (Basel, Switzerland), 10(1) (2020-01-18)
In this paper we studied the combination of advanced oxidation processes (AOPs), i.e., TiO2-based photocatalysis and photo-Fenton process, on the degradation of aqueous solutions containing a low (90 ppm) concentration of formaldehyde. Heterogeneous nanostructured catalysts, supported on polymeric nanofibers, were
Kyunghoon Choi et al.
Journal of hazardous materials, 172(2-3), 623-630 (2009-08-08)
Batch and column tests were conducted to investigate the effect of reductant concentration, reductant contact time, and suspension pH on reductive dechlorination of carbon tetrachloride (CT) by soil manipulated with Fe(II) and HS(-). Kinetic rate constants for the reductive dechlorination
Maria Valdivia-Garcia et al.
Scientific reports, 9(1), 9967-9967 (2019-07-12)
Quantitative predictions of impacts on public water supplies are essential for planning climate change adaptations. Monitoring data from five full-scale Scottish drinking water treatment plants (DWTPs) showed that significant correlations exist between conditionally carcinogenic trihalomethanes (THMs) levels, water temperature (r = 0.812

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