Saltar al contenido
Merck

239607

Sigma-Aldrich

Bromoetano

ReagentPlus®, ≥99%

Sinónimos:

Bromuro de etilo

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización


About This Item

Fórmula empírica (notación de Hill):
C2H5Br
Número de CAS:
Peso molecular:
108.97
Beilstein/REAXYS Number:
1209224
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21

vapor density

~3.75 (vs air)

Quality Level

vapor pressure

25.32 psi ( 55 °C)
7.54 psi ( 20 °C)

product line

ReagentPlus®

assay

≥99%

form

liquid

autoignition temp.

952 °F

expl. lim.

11.25 %

refractive index

n20/D 1.425 (lit.)

bp

37-40 °C (lit.)

mp

−119 °C (lit.)

density

1.46 g/mL at 25 °C (lit.)

SMILES string

CCBr

InChI

1S/C2H5Br/c1-2-3/h2H2,1H3

InChI key

RDHPKYGYEGBMSE-UHFFFAOYSA-N

¿Está buscando productos similares? Visita Guía de comparación de productos

Application

  • Inhibition of hydrogen-air mixtures by using chemical vapor additives: Compares the effectiveness of bromoethane and other brominated hydrocarbons in minimizing hydrogen hazards (SK Das et al., 2024).

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Flam. Liq. 2 - Ozone 1

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

-9.4 °F - closed cup

flash_point_c

-23 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves


Elija entre una de las versiones más recientes:

Certificados de análisis (COA)

Lot/Batch Number

¿No ve la versión correcta?

Si necesita una versión concreta, puede buscar un certificado específico por el número de lote.

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

Microwave Spectrum, Structure, and Quadrupole Coupling Constant Tensor of Ethyl Bromide.
Flanagan C and Pierce L.
J. Chem. Phys. , 38(12), 2963-2969 (1963)
J R Bucher et al.
Toxicology and applied pharmacology, 130(1), 169-173 (1995-01-01)
Chloroethane and bromoethane have been shown to cause a marked uterine tumor response in B6C3F1 mice exposed for 2 years. These chemicals are nearly unique in this regard among the nearly 400 chemicals studied by the National Toxicology Program, and
Mónica Martínez-Avilés et al.
The journal of physical chemistry. A, 111(45), 11652-11660 (2007-10-19)
A mechanism for the atmospheric oxidation of bromoethane is proposed from an ab initio study. Using CCSD(T)/6-311++G(2df,2p)//MP2/6-31G(d) level of theory, the structure and energetics of the 35 species and transition states involved in the atmospheric oxidation of bromoethane are examined.
Paula Teper-Bamnolker et al.
Plant physiology, 158(4), 2053-2067 (2012-03-01)
Potato (Solanum tuberosum) tuber, a swollen underground stem, is used as a model system for the study of dormancy release and sprouting. Natural dormancy release, at room temperature, is initiated by tuber apical bud meristem (TAB-meristem) sprouting characterized by apical
Kenneth C Westaway et al.
The journal of physical chemistry. A, 112(41), 10264-10273 (2008-09-26)
Nucleophile (11)C/ (14)C [ k (11)/ k (14)] and secondary alpha-deuterium [( k H/ k D) alpha] kinetic isotope effects (KIEs) were measured for the S N2 reactions between tetrabutylammonium cyanide and ethyl iodide, bromide, chloride, and tosylate in anhydrous

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico