UNII:M69LGV465C

Modify Date: 2024-01-02 17:09:32

UNII:M69LGV465C Structure
UNII:M69LGV465C structure
Common Name UNII:M69LGV465C
CAS Number 76792-22-8 Molecular Weight 181.028
Density 1.5±0.1 g/cm3 Boiling Point 230.0±0.0 °C at 760 mmHg
Molecular Formula C5H9BrO2 Melting Point 35-40ºC(lit.)
MSDS Chinese USA Flash Point 107.2±0.0 °C
Symbol GHS05 GHS07
GHS05, GHS07
Signal Word Danger

 Names

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

 Chemical & Physical Properties

Density 1.5±0.1 g/cm3
Boiling Point 230.0±0.0 °C at 760 mmHg
Melting Point 35-40ºC(lit.)
Molecular Formula C5H9BrO2
Molecular Weight 181.028
Flash Point 107.2±0.0 °C
Exact Mass 179.978592
PSA 37.30000
LogP 1.73
Vapour Pressure 0.0±0.9 mmHg at 25°C
Index of Refraction 1.487

 Safety Information

Symbol GHS05 GHS07
GHS05, GHS07
Signal Word Danger
Hazard Statements H302-H312-H314-H332
Precautionary Statements P280-P305 + P351 + P338-P310
Personal Protective Equipment Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard Codes C
Risk Phrases R20/21/22
Safety Phrases 26-27-28-36/37/39-45
RIDADR UN 3261 8/PG 2
WGK Germany 3.0
Hazard Class 8.0
HS Code 2915900090

 Customs

HS Code 2915900090
Summary 2915900090 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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