Home > Name List By 2 > 2-aminobutanoic acid

CAS No 80-60-4 , 2-aminobutanoic acid

  • Name: 2-aminobutanoic acid
  • Synonyms: 2-Aminobutanoic acid; DL-2-Amino-n-butyric acid; 2-Aminobutyric acid;2-aminobutanoic acid;DL-2-Aminobutyric acid; ALPHA-AMINOBUTYRIC ACID; 2835-81-6; 2-amino-; Butyrine; Butanoic acid;
  • CAS Registry Number:
  • Density: 1.106 g/cm3
  • Safety Statements: S22
  • EINECS: 201-296-6
  • Molecular Weight: 103.11976
  • InchiKey: QWCKQJZIFLGMSD-UHFFFAOYSA-N
  • InChI: InChI=1S/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)
  • Molecular Formula: C4H9NO2
  • Molecular Structure:CAS No:80-60-4 2-aminobutanoic acid

Related products

Search by region :

Select to

80-60-4 2-AMINOBUTYRIC ACID

  • Germany CHEMOS GmbH [Manufacturer]
  • Tel: 0049 9402/9336 0
  • Fax: 0049 9402/9336 13
  • Address: CHEMOS GmbH
    Werner-von-Siemensstr. 3
    93128 Regenstauf
    Germany null,nullGermany
Contact Supplier

80-60-4 2-Aminobutyric acid

  • China Beijing F&F Chemical Co.,Ltd. null
  • Fax: 86 10 64446915
  • Address: Rm.B806 HuaShiLong Building, No.37 East Road North SanHuan,Beijing 100029 China. null,nullChina
Contact Supplier

80-60-4 2-AMINOBUTANOIC ACID

  • China Nanjing Chemlin Chemical Industry Co.,Ltd. [Manufacturer]
  • Tel: +86 25 8369-7070/ +86 138 51816776 (Mobile)
  • Fax: +86 25 8345-3275
  • Address: Rm.902 Longyin Plaza,
    No. 217 Zhongshan Rd.
    (N)Nanjing 210009,China null,nullChina
Contact Supplier

Select to

1/1
References of 2-aminobutanoic acid
Title: a-Aminobutyric Acid
CAS Registry Number: 80-60-4
CAS Name: 2-Aminobutanoic acid
Synonyms: a-amino-n-butyric acid
Molecular Formula: C4H9NO2
Molecular Weight: 103.12
Percent Composition: C 46.59%, H 8.80%, N 13.58%, O 31.03%
Line Formula: CH3CH2CH(NH2)COOH
Literature References: Prepn of the DL-form from a-bromobutyric acid and ammonia: Fisher, Mounegrat, Ber. 33, 2388 (1900); from potassium cyanide, ammonium chloride and propionaldehyde: Zelinsky, Stadnikow, Ber. 41, 2062 (1908); by reduction of a-oxobutyric acid: Knoop, Oesterlin, Z. Physiol. Chem. 148, 305 (1925); from a-ethylacetoacetic ester and hydrazoic acid: Schmidt, Ber. 57, 706 (1924). The L(+)-form has been isolated from proteins: Oikawa, Chem. Zentralbl. 1926, 1, 148. Configuration: Clough, J. Chem. Soc. 113, 544, 551; Levene, Chem. Rev. 2, 203 (1926); Vogler, Helv. Chim. Acta 30, 1766 (1947).
 
Derivative Type: DL-Form
Properties: Crystals, mp 304° (begins to sublime when heated above 300°). Sol in water. One liter of water will dissolve 210.5 g at 25°. Sparingly sol in alcohol. One liter of boiling ethanol dissolves about 1.8 g. Insol in ether.
Melting point: mp 304° (begins to sublime when heated above 300°)
 
Derivative Type: DL-Form ethyl ester
Properties: Viscous liquid. bp11 61°. Sol in water and in organic solvents.
Boiling point: bp11 61°
 
Derivative Type: L-Form
Properties: Leaflets from dil alc. Sweet taste. mp 270-280° (depending on speed of heating, see Vogler, loc. cit.). [M]D +21.2° (5N HCl); [M]D +43.3° (glacial acetic acid). [a]D16 +8.40° (c = 4); [a]D16 +18.65° (c = 4.8 in 6N HCl).
Melting point: mp 270-280° (depending on speed of heating, see Vogler, loc. cit.)
Optical Rotation: [a]D16 +8.40° (c = 4); [a]D16 +18.65° (c = 4.8 in 6N HCl)
 
Derivative Type: L-Form hydrochloride
Properties: Needles; [a]D19 +12.90° (c = 3.64). Readily sol in water.
Optical Rotation: [a]D19 +12.90° (c = 3.64)