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Safety Information

307572

Sigma-Aldrich

Propionyl bromide

97%

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About This Item

Linear Formula:
CH3CH2COBr
CAS Number:
Molecular Weight:
136.98
Beilstein:
1736651
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

liquid

refractive index

n20/D 1.455 (lit.)

bp

103-104 °C (lit.)

density

1.521 g/mL at 25 °C (lit.)

functional group

acyl bromide

SMILES string

CCC(Br)=O

InChI

1S/C3H5BrO/c1-2-3(4)5/h2H2,1H3

InChI key

RIBFXMJCUYXJDZ-UHFFFAOYSA-N

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Pictograms

FlameCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Flam. Liq. 3 - Skin Corr. 1B

Supplementary Hazards

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

125.6 °F - closed cup

Flash Point(C)

52 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

307572-BULK:
307572-25G:
307572-5G:
307572-VAR:


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Molecular structure, composition, and energy and entropy differences between conformers of propionyl bromide as determined by gas-phase electron diffraction.
The Journal of Physical Chemistry, 91(15), 3977-3981 (1987)
Aniruddha Pal et al.
International journal of biological macromolecules, 119, 954-961 (2018-08-05)
Dextrin and poly (N-vinyl caprolactam) based amphiphilic graft copolymer has recently been developed using RAFT polymerization. The prepared graft copolymer has been characterized in details using FTIR and 1H NMR spectral analyses, GPC, TGA, FESEM, TEM and DLS analyses. GPC
Hasmik Grigoryan et al.
Carcinogenesis, 39(5), 661-668 (2018-03-15)
Although benzene has long been recognized as a cause of human leukemia, the mechanism by which this simple molecule causes cancer has been problematic. A complicating factor is benzene metabolism, which produces many reactive intermediates, some specific to benzene and

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