Skip to Content
Merck
All Photos(1)

Documents

167118

Sigma-Aldrich

Ethyl 4-bromobutyrate

95%

Synonym(s):

γ-Bromobutyric acid ethyl ester, 1-Bromo-3-(carboethoxy)propane, 3-(Ethoxycarbonyl)propyl bromide, 4-Bromobutanoic acid ethyl ester, 4-Bromobutyric acid ethyl ester, Ethyl γ-bromobutyrate, Ethyl 4-bromobutanoate

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
Br(CH2)3COOC2H5
CAS Number:
Molecular Weight:
195.05
Beilstein:
1749700
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

95%

form

liquid

refractive index

n20/D 1.456 (lit.)

bp

80-82 °C/10 mmHg (lit.)

density

1.363 g/mL at 25 °C (lit.)

SMILES string

CCOC(=O)CCCBr

InChI

1S/C6H11BrO2/c1-2-9-6(8)4-3-5-7/h2-5H2,1H3

InChI key

XBPOBCXHALHJFP-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Ethyl 4-bromobutyrate was used in Enzyme-linked immunosorbent assay for zilpaterol. It was used in the synthesis of isosteric thieno[2,3-b]-azepin-4-ones, having anti-tumor activity. It was also used in the synthesis of poly(2,6-dimethyl-1,4-phenylene oxide).

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

195.8 °F - closed cup

Flash Point(C)

91 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

R F Koebel et al.
Journal of medicinal chemistry, 18(2), 192-194 (1975-02-11)
In view of the antitumor activity reported for 7,8-dimethylbenzo[b]azepine-2,5-dione, new isosteric thieno[2,3-b]-azepin-4-ones have been prepared by a Dieckmann ring closure reaction. Substituted 2-amino-3-carbethoxythiophenes were tosylated, or benzoylated, and the corresponding sodium salt was alkylated with ethyl 4-bromobutyrate. The resulting product
Prithidipa Sahoo et al.
Bioorganic chemistry, 71, 315-324 (2017-03-14)
Naphthyridine-based fluorescent probe H1 was synthesized and characterized for the quantification and selective detection of Uric Acid (UA) in live cell. In presence of UA, H1 forms the specific host-guest complex mainly through intermolecular hydrogen bonding and aromatic stacking which
Weilin L Shelver et al.
Journal of agricultural and food chemistry, 52(8), 2159-2166 (2004-04-15)
Zilpaterol is an beta-adrenergic agonist approved for use in cattle in South Africa and Mexico as a growth promoter. It is not currently approved for use in the EU, USA, or Asia. Here, we report the development of an ELISA
Xingdong Yang et al.
Scientific reports, 8(1), 16680-16680 (2018-11-14)
A lateral flow immunochromatographic strip test (LFIST) based on a competitive format was developed for rapid and sensitive on-site detection of oseltamivir phosphate (OP) residues in poultry product. The sensitivity (half inhibitory concentration, IC50) of the LFIST in the detection
Evan Wenbo Zhao et al.
Journal of the American Chemical Society, 143(4), 1885-1895 (2021-01-22)
We report the development of in situ (online) EPR and coupled EPR/NMR methods to study redox flow batteries, which are applied here to investigate the redox-active electrolyte, 2,6-dihydroxyanthraquinone (DHAQ). The radical anion, DHAQ3-•, formed as a reaction intermediate during the

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