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CAS No 56-12-2 , 4-aminobutanoic acid

  • Name: 4-aminobutanoic acid
  • Synonyms: 4-aminobutyric acid; GABA; Piperidic acid; Aminalon; Piperidinic acid; gamma-aminobutyric acid;4-aminobutanoic acid; Gammalon; Gaballon;4-Aminobutanoic acid;
  • CAS Registry Number:
  • Melting Point: 195-204 ºC
  • Flash Point: 103.8 ºC
  • Boiling Point: 248ºC at 760 mmHg
  • Refractive index: 1.465
  • Safety Statements: R36/37/38
  • Hazard Symbols: Xi: Irritant;
  • HS Code: 29224995
  • Flash Point: 103.8 ºC
  • EINECS: 200-258-6
  • Molecular Weight: 103.11976
  • InchiKey: BTCSSZJGUNDROE-UHFFFAOYSA-N
  • InChI: InChI=1S/C4H9NO2/c5-3-1-2-4(6)7/h1-3,5H2,(H,6,7)
  • Risk Statements: S26;S36
  • Molecular Formula: C4H9NO2
  • Molecular Structure:CAS No:56-12-2 4-aminobutanoic acid

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56-12-2 4-AMINOBUTYRIC ACID

  • United States Advanced Synthesis Technologies [Manufacturer]
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56-12-2 GAMMA AMINOBUTYRIC ACID

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56-12-2 4-AMINOBUTYRIC ACID (GABA)

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56-12-2 AMINOBUTYRIC ACID (GAMMA-)

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56-12-2 纬-Aminobutyric acid

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56-12-2 g-Amino Butyric Acid (GABA)

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56-12-2 01-24350 4-AMINOBUTYRIC ACID

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56-12-2 4-Aminobutyric acid

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56-12-2 Boc-beta-homoalanine

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56-12-2 4-Aminobutyric acid

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References of 4-aminobutanoic acid
Title: g-Aminobutyric Acid
CAS Registry Number: 56-12-2
CAS Name: 4-Aminobutanoic acid
Synonyms: g-amino-n-butyric acid; piperidic acid; GABA
Trademarks: Gammalon (Daiichi)
Molecular Formula: C4H9NO2
Molecular Weight: 103.12
Percent Composition: C 46.59%, H 8.80%, N 13.58%, O 31.03%
Line Formula: H2NCH2CH2CH2COOH
Literature References: Nonprotein amino acid that functions as a neurotransmitter. Prepn from succinimide: Tafel, Stern, Ber. 33, 2224 (1900); from piperylurethan and fuming nitric acid: Schotten, Ber. 16, 643 (1883); Abderhalden, Chem. Zentralbl. 1926, II, 779; from N-(b-bromoethyl)phthalimide and sodiomalonic ester: Aschan, Ber. 24, 2450 (1891); from g-chlorobutyronitrile and potassium phthalimide: Gabriel, Ber. 22, 3335 (1889); 23, 1771 (1890); DeWitt, Org. Synth. coll. vol. II, 25 (1943). Review of biochemical pharmacology: R. Tapia in Handbook of Psychopharmacology, L. L. Iversen et al., Eds. (Plenum, New York, 1975) pp 1-58; L. L. Iversen in Psychopharmacology: A Generation of Progress, M. A. Lipton et al., Eds. (Raven, New York, 1978) pp 25-38; C. C. Mao, E. Costa, ibid. pp 307-318.
Properties: Leaflets from methanol + ether, needles from water + alcohol, mp 202° (dec on rapid heating). Ka 3.7 ′ 10-11; Kb 1.7 ′ 10-10 at 25°. Freely sol in water. Insol or poorly sol in other solvents. On melting it dec forming pyrrolidone and water.
Melting point: mp 202° (dec on rapid heating)
 
Derivative Type: Hydrochloride
Molecular Formula: C4H9NO2.HCl
Molecular Weight: 139.58
Percent Composition: C 34.42%, H 7.22%, N 10.03%, O 22.93%, Cl 25.40%
Properties: Crystals, mp 135-136°.
Melting point: mp 135-136°
 
Derivative Type: Ethyl ester
Molecular Formula: C6H13NO2
Molecular Weight: 131.17
Percent Composition: C 54.94%, H 9.99%, N 10.68%, O 24.39%
Properties: Liquid, bp12 76°.
Boiling point: bp12 76°
 
Therap-Cat: Antihypertensive.
Keywords: Antihypertensive.