UNII:M69LGV465C

Modify Date: 2024-01-04 07:20:19

UNII:M69LGV465C Structure
UNII:M69LGV465C structure
Common Name UNII:M69LGV465C
CAS Number 565-74-2 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 39-42 °C(lit.)
MSDS Chinese USA Flash Point 107.2±0.0 °C
Symbol GHS05 GHS07
GHS05, GHS07
Signal Word Danger

 Names

Name 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 39-42 °C(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

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
ES8055000
CHEMICAL NAME :
Butyric acid, 2-bromo-3-methyl-
CAS REGISTRY NUMBER :
565-74-2
LAST UPDATED :
199710
DATA ITEMS CITED :
5
MOLECULAR FORMULA :
C5-H9-Br-O2

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
769 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
EPASR* United States Environmental Protection Agency, Office of Pesticides and Toxic Substances. (U.S. Environmental Protection Agency, 401 M St., SW, Washington, DC 20460) History unknown. Volume(issue)/page/year: 8EHQ-0188-0714
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Administration onto the skin
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
1410 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
EPASR* United States Environmental Protection Agency, Office of Pesticides and Toxic Substances. (U.S. Environmental Protection Agency, 401 M St., SW, Washington, DC 20460) History unknown. Volume(issue)/page/year: 8EHQ-0188-0714 ** OTHER MULTIPLE DOSE TOXICITY DATA **
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
17600 mg/kg/4W-I
TOXIC EFFECTS :
Related to Chronic Data - death
REFERENCE :
EPASR* United States Environmental Protection Agency, Office of Pesticides and Toxic Substances. (U.S. Environmental Protection Agency, 401 M St., SW, Washington, DC 20460) History unknown. Volume(issue)/page/year: 8EHQ-0188-0714

 Safety Information

Symbol GHS05 GHS07
GHS05, GHS07
Signal Word Danger
Hazard Statements H302 + H312-H314
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 R21/22;R34
Safety Phrases S26-S36/37/39-S45
RIDADR UN 3261 8/PG 2
WGK Germany 3
RTECS ES8055000
Packaging Group III
Hazard Class 8
HS Code 29159080

 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%

 Articles4

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

DL-2-Bromoisovaleric acid
2-Bromo-3-methylbutyric acid
Butanoic acid, 2-bromo-3-methyl-
dl-2-bromo-3-methylbutyric acid
2-BROMOISOVALERIC ACID
(±)-2-BROMO-3-METHYLBUTYRIC ACID
α-Bromoisovaleric acid
A-BROMOISOVALERIC ACID
2-broMo acid
EINECS 209-291-0
MFCD00004210
Isovaleric acid, α-bromo-
2-BROMOISOPENTANOIC ACID
2-Bromo-3-methylbutanoic acid
2-Bromo-iso-acid
a-Bromoisopentanoic acid
UNII:M69LGV465C
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