CAS 76792-22-8|UNII:M69LGV465C

Introduction:Basic information about CAS 76792-22-8|UNII:M69LGV465C, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameUNII:M69LGV465C
CAS Number76792-22-8Molecular Weight181.028
Density1.5±0.1 g/cm3Boiling Point230.0±0.0 °C at 760 mmHg
Molecular FormulaC5H9BrO2Melting Point35-40ºC(lit.)
MSDSChineseUSAFlash Point107.2±0.0 °C
Symbol
GHS05, GHS07
Signal WordDanger

Names

Name(R)-(+)-2-Bromo-3-Methylbutyric Acid
SynonymMore Synonyms

Chemical & Physical Properties

Density1.5±0.1 g/cm3
Boiling Point230.0±0.0 °C at 760 mmHg
Melting Point35-40ºC(lit.)
Molecular FormulaC5H9BrO2
Molecular Weight181.028
Flash Point107.2±0.0 °C
Exact Mass179.978592
PSA37.30000
LogP1.73
Vapour Pressure0.0±0.9 mmHg at 25°C
Index of Refraction1.487
InChIKeyUEBARDWJXBGYEJ-SCSAIBSYSA-N
SMILESCC(C)C(Br)C(=O)O

Safety Information

Symbol
GHS05, GHS07
Signal WordDanger
Hazard StatementsH302-H312-H314-H332
Precautionary StatementsP280-P305 + P351 + P338-P310
Personal Protective EquipmentFaceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard CodesC
Risk PhrasesR20/21/22
Safety Phrases26-27-28-36/37/39-45
RIDADRUN 3261 8/PG 2
WGK Germany3.0
Hazard Class8.0
HS Code2915900090

Customs

HS Code2915900090
Summary2915900090 other saturated acyclic monocarboxylic acids and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:5.5% General tariff:30.0%

Articles3

More Articles
Glutathione conjugation of the alpha-bromoisovaleric acid enantiomers in the rat in vivo and its stereoselectivity. Pharmacokinetics of biliary and urinary excretion of the glutathione conjugate and the mercapturate.

Biochem. Pharmacol. 38(22) , 3957-62, (1989)

The glutathione (GSH) conjugation of (R)-and (S)-alpha-bromoisovaleric acid (BI) in the rat in vivo, and its stereoselectivity, have been characterized. After administration of racemic [1-14C]BI two r...

Stereoselectivity of rat liver glutathione transferase isoenzymes for alpha-bromoisovaleric acid and alpha-bromoisovalerylurea enantiomers.

Biochem. J. 252(1) , 137-42, (1988)

The stereoselectivity of purified rat GSH transferases towards alpha-bromoisovaleric acid (BI) and its amide derivative alpha-bromoisovalerylurea (BIU) was investigated. GSH transferase 2-2 was the on...

Stereoselective conjugation of 2-bromocarboxylic acids and their urea derivatives by rat liver glutathione transferase 12-12 and some other isoforms.

Biochem. Pharmacol. 44(7) , 1249-53, (1992)

Glutathione (GSH) conjugation of the separate enantiomers of five 2-bromocarboxylic acids and some of their urea derivatives by rat liver GSH transferases (GSTs) was studied. The liver cytosolic fract...

Synonyms

MFCD00210113
R-2-Bromo-3-methylbutyric acid
2-Bromo-3-methylbutyric acid
Butanoic acid, 2-bromo-3-methyl-
α-Bromoisovaleric acid
(±)-2-BROMO-3-METHYLBUTYRIC ACID
(R)-(+)-2-Bromo-3-methylbutyric acid
α-BROMOISOVALERIC ACID, (R)-
(2R)-2-bromo-3-methyl-butanoic acid
Isovaleric acid, α-bromo-
2-Bromo-3-methylbutanoic acid
(2R)-2-Bromo-3-methylbutanoic acid
Butanoic acid, 2-bromo-3-methyl-, (2R)-
(R)-(+)-2-BROMO 3-METHYLBUTANOIC ACID
UNII:M69LGV465C
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