alpha-HYDROXY-ISOBUTYRIC ACID

PRODUCT IDENTIFICATION

CAS NO. 594-61-6

alpha-HYDROXY-ISOBUTYRIC ACID

EINECS NO. 209-848-8
FORMULA (CH3)2C(OH)COOH
MOL WT. 104.11
H.S. CODE  
TOXICITY  
SYNONYMS 2-Hydroxy-2-methylpropanoic acid; 2-Methyllactic acid;
2-Hydroxy-2-methylpropionic acid; 2-Hydroxyisobutyric acid; Acetonic acid; Hydroxydimethylacetic acid; ácido 2-hidroxi-2-metilpropionico; Acide 2-hydroxy-2-méthylpropionique;
RAW MATERIALS
 

CLASSIFICATION

 

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE

white to off-white crystalline powder

MELTING POINT 77 - 81 C
BOILING POINT 212 C
SPECIFIC GRAVITY

 

SOLUBILITY IN WATER 1900 g/l (soluble in methanol, diethyl ether, sparingly soluble in benzene)
AUTOIGNITION

 

pH  
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FLASH POINT

 

STABILITY Stable under ordinary conditions. Hygroscopic.

APPLICATIONS

n-Butyric acid is a saturated four-carbon carboxylic acid which is a clear liquid, with a suffocating odor and with melting point -6 C and boiling point 164 C. It occurs naturally in rancid butter, in much animal fat and in plant oil. It is soluble in water, ethanol and ether. It can be obtained by the fermentation of sugar or starch, brought about by the addition calcium carbonate or by the oxidation of butanol in the presence of potassium permanganate. There is a structural formula called isobutyric acid which can not be obtained by the fermentation but by the oxidation of isopropyl alcohol with potassium bichromate and sulfuric acid. Isobutyric acid melts at -47 C and boils at 154 C. It is slightly soluble in water but soluble in ethanol, ether and organic solvents. Butyric acid is a strong acid and reacts with bases, strong oxidants and metals. It is used to eliminate calcium in leather industry. Butyric acid family products, such as their esters, are used for the production of plastics, plasticizers, surfactants and textile auxiliaries. They are used in food additives, flavorings, varnishes, perfumes, pharmaceuticals and disinfectants. Aminobutyric acid is a four-carbon carboxylic acid, to which an amino group is attached. There are three structural isomers, alpha, beta, gamma-. Alpha-aminobutyric acid is has an amino group substituted at the alpha, or 1 position on the carbon atom next to the acid group, while gamma-aminobutyric acid (GABA) at the terinal carbon (the gamma, or 4 position). Natural GABA exits in L-form only and can be found in plant and animal tissues. It is formed in the metabolism of L-glutamic acid.  It is the central nervous system postsynaptic inhibitory transmitter in the brain but is also found in several extraneural tissues, including kidney and pancreatic islet beta cells. Gamma- hydroxy butyric acid is an intermediate occurring in metabolism of GABA. There are several hydroxy butyric acid occur at elevated levels in some metabolic disorders.  In biological systems The GABA family products are the parent compounds for a number of psychoactive drugs covering sedation/hypnosis, anxiolysis, anticonvulsant activity, muscle relaxation and anterograde amnesia. Some examples are benzodiazepines, baclofen, bicuculline, barbiturates, picrotoxin, neurosteroids and the general anesthetics.
SALES SPECIFICATION

APPEARANCE

white to off-white crystalline powder

CONTENT

98.0% min

MELTING POINT

77 - 81 C
TRANSPORTATION
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HAZARD CLASS  
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OTHER INFORMATION
Hazard Symbols: XI, Risk Phrases: 37/38-41, Safety Phrases: 26-39