(S)-(-)-2-Bromo-3-methylbutyric acid
Names
[ CAS No. ]:
26782-75-2
[ Name ]:
(S)-(-)-2-Bromo-3-methylbutyric acid
[Synonym ]:
MFCD00210114
α-BROMOISOVALERIC ACID, (S)-
(2S)-2-bromo-3-methyl-butanoic acid
2-Bromo-3-methylbutyric acid
Butanoic acid, 2-bromo-3-methyl-
2S-2-bromo-3-methylbutanoic acid
(2S)-2-Bromo-3-methylbutanoic acid
α-Bromoisovaleric acid
(±)-2-BROMO-3-METHYLBUTYRIC ACID
(S)-2-Bromoisovaleric acid
Isovaleric acid, α-bromo-
2-Bromo-3-methylbutanoic acid
(S)-2-Bromo-3-methylbutyric acid
Butanoic acid, 2-bromo-3-methyl-, (2S)-
(S)-(-)-2-Bromo-3-methylbutyric acid
S-2-Bromo-3-methyl-butyric acid
UNII:M69LGV465C
Chemical & Physical Properties
[ Density]:
1.5±0.1 g/cm3
[ Boiling Point ]:
230.0±0.0 °C at 760 mmHg
[ Melting Point ]:
39-44ºC
[ 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
[ Signal Word ]:
Danger
[ Hazard Statements ]:
H302-H312-H314-H332
[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310
[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges
[ Hazard Codes ]:
C: Corrosive;
[ Risk Phrases ]:
R20/21/22;R34
[ Safety Phrases ]:
S26-S27-S28-S36/37/39-S45
[ RIDADR ]:
UN 3261
[ HS Code ]:
2915900090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
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%
Articles
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...