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CAS No 133-32-4 , 4-(1H-indol-3-yl)butanoic acid Search by region : Germany

  • Name: 4-(1H-indol-3-yl)butanoic acid
  • Synonyms: Indolebutyric acid; 133-32-4; Indole-3-butanoic acid;4-(1H-indol-3-yl)butanoic acid; Seradix; Hormodin; 1H-INDOLE-3-BUTANOIC ACID;Indole-3-butyric acid; 3-Indolebutyric acid;
  • CAS Registry Number:
  • Transport: UN 2811 6.1/PG 3
  • Melting Point: 120-125 ºC
  • Density: 1.252 g/cm3
  • Safety Statements: R25;R36/37/38
  • Hazard Symbols: T: Toxic;
  • HS Code: 29339990
  • EINECS: 205-101-5
  • Molecular Weight: 203.23712
  • InchiKey: JTEDVYBZBROSJT-UHFFFAOYSA-N
  • InChI: InChI=1S/C12H13NO2/c14-12(15)7-3-4-9-8-13-11-6-2-1-5-10(9)11/h1-2,5-6,8,
    13H,3-4,7H2,(H,14,15)
  • Risk Statements: S26;S28A;S36/37/39;S38;S45
  • Molecular Formula: C12H13NO2
  • Molecular Structure:CAS No:133-32-4 4-(1H-indol-3-yl)butanoic acid

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133-32-4 3-Indolebutyric acid

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References of 4-(1H-indol-3-yl)butanoic acid
Title: Indolebutyric Acid
CAS Registry Number: 133-32-4
CAS Name: 1H-Indole-3-butanoic acid
Synonyms: indole-3-butyric acid; 4-(3-indolyl)butyric acid
Trademarks: Seradix (Rhone-Poulenc)
Molecular Formula: C12H13NO2
Molecular Weight: 203.24
Percent Composition: C 70.92%, H 6.45%, N 6.89%, O 15.74%
Literature References: Prepn: Jackson, Manske, J. Am. Chem. Soc. 52, 5029 (1930); by heating indole, g-butyrolactone, and sodium hydroxide, followed by acidification of the product: Fritz, US 3051723 (1962 to Union Carbide); by decarboxylation of 2-carboxyindole-3-butyric acid: Bowman, Islip, Chem. Ind. (London) 1971, 154. Toxicity studies: Anderson et al., Proc. Soc. Exp. Biol. Med. 34, 138 (1936); Pesonen, Acta Endocrinol. 5, 409 (1950). Hypoglycemic effect in rats: Mirsky et al., Endocrinology 59, 715 (1956).
Properties: White or slightly yellow crystals. Slight characteristic odor. mp 123-125°. Practically insol in water, chloroform. Sol in alc, ether, acetone. LD50 i.p. in mice: 100 mg/kg (Anderson).
Melting point: mp 123-125°
Toxicity data: LD50 i.p. in mice: 100 mg/kg (Anderson)
Use: To stimulate root formation of plant clippings.