<Suppliers Price>

Sodium 2-oxobutanoate

Names

[ CAS No. ]:
2013-26-5

[ Name ]:
Sodium 2-oxobutanoate

[Synonym ]:
Butanoic acid, 2-oxo-, sodium salt (1:1)
Butanoic acid,2-oxo-,sodium salt
sodium 2-ketobutyric acid
SodiuM 2-Oxobutyrate
MFCD00064194
2-Oxobutanoic acid sodium salt
BUTYRIC ACID,2-OXO-,SODIUM SALT
2-oxobuttersaeure,natrium salz
Sodium 2-Ketobutyrate
EINECS 217-937-8
2-Oxobutyric Acid Sodium Salt
2-Ketobutyric Acid Sodium Salt
Sodium 2-oxobutanoate
2-oxobutyric acid,sodium salt
Alpha-Ketobutyric Acid Sodium Salt

Biological Activity

[Description]:

Sodium 2-oxobutanoate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Chemical & Physical Properties

[ Density]:
1.182g/cm3

[ Boiling Point ]:
177.8ºC at 760mmHg

[ Melting Point ]:
210°C

[ Molecular Formula ]:
C4H5NaO3

[ Molecular Weight ]:
124.071

[ Flash Point ]:
65ºC

[ Exact Mass ]:
124.013641

[ PSA ]:
57.20000

[ Appearance of Characters ]:
powder | white

[ Vapour Pressure ]:
0.0331mmHg at 25°C

[ Storage condition ]:
2-8°C

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
ET5955900
CHEMICAL NAME :
Butyric acid, 2-oxo-, sodium salt
CAS REGISTRY NUMBER :
2013-26-5
LAST UPDATED :
199701
DATA ITEMS CITED :
3
MOLECULAR FORMULA :
C4-H5-O3.Na
MOLECULAR WEIGHT :
124.08
WISWESSER LINE NOTATION :
OVV2 &-NA-

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
2960 mg/kg
TOXIC EFFECTS :
Behavioral - somnolence (general depressed activity)
REFERENCE :
FATOAO Farmakologiya i Toksikologiya (Moscow). For English translation, see PHTXA6 and RPTOAN. (V/O Mezhdunarodnaya Kniga, 113095 Moscow, USSR) V.2- 1939- Volume(issue)/page/year: 42,221,1979 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - X9819 No. of Facilities: 147 (estimated) No. of Industries: 1 No. of Occupations: 2 No. of Employees: 2044 (estimated) No. of Female Employees: 1461 (estimated)

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ RTECS ]:
ET5955900

[ HS Code ]:
2918300090

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2918300090

[ Summary ]:
2918300090 other carboxylic acids with aldehyde or ketone function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

Articles

Kinetic resolution of 2-hydroxybutanoate racemic mixtures by NAD-independent L-lactate dehydrogenase.

Bioresour. Technol. 102(7) , 4595-9, (2011)

Optically active D-2-hydroxybutanoate is an important building block intermediate for medicines and biodegradable poly(2-hydroxybutanoate). Kinetic resolution of racemic 2-hydroxybutanoate may be a gr...

Transaminase-catalyzed asymmetric synthesis of L-2-aminobutyric acid from achiral reactants.

Biotechnol. Lett. 31 , 1595-1599, (2009)

Asymmetric synthesis of an unnatural amino acid was demonstrated by omega-transaminase from Vibrio fluvialis JS17. L-2-Aminobutyric acid was synthesized from 2-oxobutyric acid and benzylamine with an ...

Expanding metabolism for total biosynthesis of the nonnatural amino acid L-homoalanine.

Proc. Natl. Acad. Sci. U. S. A. 107(14) , 6234-9, (2010)

The dramatic increase in healthcare cost has become a significant burden to the world. Many patients are denied the accessibility of medication because of the high price of drugs. Total biosynthesis o...


More Articles


Related Compounds

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.