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232750

Sigma-Aldrich

1-Bromo-2-chloroethane

98%

Synonym(s):

Ethylene bromochloride, Ethylene chlorobromide

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1 KIT
$896.00

About This Item

Linear Formula:
ClCH2CH2Br
CAS Number:
Molecular Weight:
143.41
Beilstein:
605265
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

form:
liquid
Assay:
98%

$896.00


Estimated to ship onMarch 29, 2025


Request a Bulk Order

Quality Level

Assay

98%

form

liquid

refractive index

n20/D 1.488 (lit.)

bp

106-107 °C (lit.)

mp

−18-−14 °C (lit.)

solubility

water: soluble

density

1.723 g/mL at 25 °C (lit.)

functional group

bromo
chloro

SMILES string

ClCCBr

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This Item
RAB1784RAB1789RAB1780
assay range

inter-assay cv: <12%
intra-assay cv: <10%

assay range

inter-assay cv: <12%
intra-assay cv: <10%

assay range

inter-assay cv: <12%
intra-assay cv: <10%

assay range

inter-assay cv: <12%
intra-assay cv: <10%

technique(s)

ELISA: suitable

technique(s)

ELISA: suitable

technique(s)

ELISA: suitable

technique(s)

ELISA: suitable

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

shipped in

wet ice

shipped in

wet ice

shipped in

wet ice

shipped in

wet ice

General description

Dissociative double ionization and multi-photon ionization of 1-bromo-2-chloroethane (BCE) irradiated by the 800nm femtosecond laser field has been investigated by dc-slice imaging technology[1]. Conformational properties of BCE in several zeolites such as silicalite-1, siliceous Y, Na-Y and zeolite L have been investigated by FT-Raman spectroscopy[2].

Application

1-Bromo-2-chloroethane was used in regio- and diastereoselective synthesis of 2-alkylidenetetrahydrofurans[3].

Pictograms

Skull and crossbonesHealth hazard

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Carc. 1B - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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    Haiyan Wang et al.
    Langmuir : the ACS journal of surfaces and colloids, 25(14), 8042-8050 (2009-04-21)
    The conformational properties of 1-bromo-2-chloroethane (BCE) in several representative zeolites including silicalite-1, siliceous Y (Si-Y), Na-Y, and zeolite L have been investigated by FT-Raman spectroscopy in combination with thermogravimetric analysis. The results indicate that the conformational and dynamic behavior of
    P Langer et al.
    The Journal of organic chemistry, 66(18), 6057-6063 (2001-09-01)
    The domino C,O-cyclodialkylation reaction of dilithiated 1,3-dicarbonyl compounds with 1,4-dibromo-2-butene resulted in regio- and diastereoselective formation of 2-alkylidene-5-vinyltetrahydrofurans. The cyclization of 1,3-dicarbonyl dianions with 1-bromo-2-chloroethane regio- and diastereoselectively afforded 2-alkylidenetetrahydrofurans under thermodynamic reaction control.
    Yan Yang et al.
    The Journal of chemical physics, 135(6), 064303-064303 (2011-08-17)
    The dissociative double ionization and multi-photon ionization of 1-bromo-2-chloroethane (BCE) irradiated by the 800 nm femtosecond laser field have been investigated by dc-slice imaging technology. The charged parent ion ratio [BCE(2+)]/[BCE(+)] was measured, and the corresponding ionization process including non-sequential
    Y Oda et al.
    Carcinogenesis, 17(2), 297-302 (1996-02-01)
    The Escherichia coli mu operon was subcloned into a pKK233-2 vector containing rat glutathione S-transferase (GST) 5-5 cDNA and the plasmid thus obtained was introduced into Salmonella typhimurium TA1535. The newly developed strain S.typhimurium NM5004, was found to have 52-fold
    R D Storer et al.
    Carcinogenesis, 4(11), 1491-1494 (1983-11-01)
    Hepatic DNA damage was demonstrated by alkaline DNA unwinding/hydroxylapatite batch chromatography in male B6C3F1 mice treated with non-necrogenic doses of 1,2-dichloroethane, 1-bromo-2-chloroethane, and 1,2-dibromoethane. Intraperitoneal administration of 0.5 mmol/kg of 1-bromo-2-chloroethane and 1,2-dibromoethane produced similar levels of DNA damage. A

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