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Ethyl bromopyruvate

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Ethyl bromopyruvate manufacturers

  • Ethyl bromopyruvate
  • Ethyl bromopyruvate pictures
  • $75.00
  • 2026-08-25
  • CAS:70-23-5
  • Min. Order: 10kg
  • Purity: 0.99
  • Supply Ability: 20tons
Ethyl bromopyruvate Basic information
Product Name:Ethyl bromopyruvate
Synonyms:ETHYL BROMOPYRUVATE;BROMOPYRUVIC ACID ETHYL ESTER;beta-Bromopyruvic acid ethyl ester;Pyruvic acid, bromo-, ethyl ester;Ethylbromopyruvate (Tech);Propanoic acid, 3-bromo-2-oxo-, ethyl ester;ETHYL3-BROMO-2-OXOPROPANOATE(ETHYLBROMOPYRUVATE);Ethyl 3-bromopyruvate, tech. 90%
CAS:70-23-5
MF:C5H7BrO3
MW:195.01
EINECS:200-729-6
Product Categories:Aliphatics;Esters;Aromatic Esters;Building Blocks;C2 to C5;Carbonyl Compounds;C2 to C5;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks
Mol File:70-23-5.mol
Ethyl bromopyruvate Structure
Ethyl bromopyruvate Chemical Properties
Boiling point 98-100 °C10 mm Hg(lit.)
density 1.554 g/mL at 25 °C(lit.)
refractive index n20/D 1.469(lit.)
Fp 210 °F
storage temp. 2-8°C
solubility Difficult to mix.
form Liquid
color Clear yellow to pink-red
Sensitive Moisture Sensitive
BRN 1760158
InChI1S/C5H7BrO3/c1-2-9-5(8)4(7)3-6/h2-3H2,1H3
InChIKeyVICYTAYPKBLQFB-UHFFFAOYSA-N
SMILESCCOC(=O)C(=O)CBr
LogP0.861 (est)
CAS DataBase Reference70-23-5(CAS DataBase Reference)
NIST Chemistry ReferencePropanoic acid, 3-bromo-2-oxo-, ethyl ester(70-23-5)
EPA Substance Registry SystemPropanoic acid, 3-bromo-2-oxo-, ethyl ester (70-23-5)
Safety Information
Hazard Codes Xi,T
Risk Statements 36/37/38-33-23/24
Safety Statements 26-36-24/25
RIDADR 3265
WGK Germany 3
8-9-21
Hazard Note Irritant
TSCA TSCA listed
HazardClass 8
PackingGroup II
HS Code 29183000
Storage Class10 - Combustible liquids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
Ethyl bromopyruvate English
SigmaAldrich English
ACROS English
ALFA English
Ethyl bromopyruvate Usage And Synthesis
Chemical PropertiesClear yellow to pink-red liquid
UsesEthyl 3-bromopyruvate is employed in a synthesis of thioxothiazolidines from primary amines and carbon disulfide.
UsesEmployed in a synthesis of thioxothiazolidines from primary amines and carbon disulfide.1
HazardSevere poison, lachrymator, irritant.
Purification MethodsThe most likely impurity is free acid (bromopyruvic or bromoacetic acids). Dissolve the ester in dry Et2O or dry CHCl3, stir with CaCO3 until effervescence ceases, filter, (may wash with a little H2O rapidly), dry (MgSO4) and distil it at least twice. The 2,4-dinitrophenylhydrazone has m 144-145o. [Burros & Holland J Chem Soc 672 1947, Letsinger & Laco J Org Chem 21 764 1956, Kruse et al. J Am Chem Soc 76 5796 1954, Beilstein 3 IV 1519.] LACHRYMATORY.
References[1] Justus Liebigs Annalen der Chemie, 1949, vol. 564, p. 35
[2] Journal of the Chemical Society, 1947, p. 670
[3] Journal of the American Chemical Society, 1944, vol. 66, p. 1658
[4] Journal of the Chemical Society, 1947, p. 1372,1374
[5] Recueil des Travaux Chimiques des Pays-Bas, 1941, vol. 60, p. 495,500
Tag:Ethyl bromopyruvate(70-23-5) Related Product Information
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