UNII:M69LGV465C structure
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Common Name | UNII:M69LGV465C | ||
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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 |
Signal Word | Danger |
Name | (R)-(+)-2-Bromo-3-Methylbutyric Acid |
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Synonym | More Synonyms |
Density | 1.5±0.1 g/cm3 |
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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 |
Symbol |
GHS05, GHS07 |
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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 |
HS Code | 2915900090 |
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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% |
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... |
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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... |
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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... |
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 |