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CAS No 536-69-6 , 5-butylpyridine-2-carboxylic acid Search by region : Germany

  • Name: 5-butylpyridine-2-carboxylic acid
  • Synonyms: 5-Butylpicolinic acid; Picolinic acid; Fusarinic acid; 5-butyl-;5-butylpyridine-2-carboxylic acid; 5-Butylpyridine-2-carboxylic acid; 536-69-6;
  • CAS Registry Number:
  • Transport: 2811
  • Melting Point: 96-100 °C
  • Flash Point: 152.9°C
  • Boiling Point: 329.2°Cat760mmHg
  • Density: 1.113g/cm3
  • Safety Statements: A poison by ingestion, intraperitoneal, subcutaneous, and intravenous routes. When heated to decomposition it emits toxic fumes of NOx.
  • Hazard Symbols: T
  • Flash Point: 152.9°C
  • EINECS: 208-643-0
  • Molecular Weight: 179.21572
  • InchiKey: DGMPVYSXXIOGJY-UHFFFAOYSA-N
  • InChI: InChI=1S/C10H13NO2/c1-2-3-4-8-5-6-9(10(12)13)11-7-8/h5-7H,2-4H2,1H3,(H,
    12,13)
  • Risk Statements: R25;
  • Molecular Formula: C10H13NO2
  • Molecular Structure:CAS No:536-69-6 5-butylpyridine-2-carboxylic acid

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536-69-6 FUSARIC ACID

  • Germany BIOTREND Chemikalien GmbH [Manufacturer]
  • Tel: ++49 (0)2 21 9 49 83 20
  • Fax: ++49 (0)2 21 9 49 83 25
  • Address: BIOTREND Chemikalien GmbH
    Eupener Str. 157
    D - 50933 Cologne
    Germany null,nullGermany
Contact Supplier

536-69-6 5-n-Butyl-2-picolinic acid; 95%

  • 5-n-Butyl-2-picolinic acid; 95%
  • Germany ABCR GmbH & Co KG [Manufacturer]
  • Tel: +49 721 95061-0
  • Fax: +49 721 95061-80
  • Address: Im Schlehert 10
    76187 Karlsruhe
    Germany null,nullGermany
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536-69-6 Fusaric acid

  • Fusaric 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

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References of 5-butylpyridine-2-carboxylic acid
Title: Fusaric Acid
CAS Registry Number: 536-69-6
CAS Name: 5-Butyl-2-pyridinecarboxylic acid
Synonyms: 5-butylpicolinic acid
Molecular Formula: C10H13NO2
Molecular Weight: 179.22
Percent Composition: C 67.02%, H 7.31%, N 7.82%, O 17.85%
Literature References: Antibiotic (wilting agent) first isolated from the fungus Fusarium heterosporium, Nees: Yabuta et al., J. Agric. Chem. Soc. Jpn. 10, 1059 (1934). Isoln from other Fusarium species and from Gibberella fujikuroi and synthesis: Plattner et al., Helv. Chim. Acta 37, 1379 (1954). Prepn: Hardegger, Nikles, ibid. 39, 505 (1956); 40, 2428 (1957); Schreiber, Adam, Ber. 93, 1848 (1960); Umezawa, Nagatsu, DE 2005255 (1970 to Microbiochem. Res. Found.); R. Tschesche, W. Führer, Ber. 111, 3502 (1978). Dopamine b-hydroxylase inhibitor and hypotensive activity: Suda et al., Chem. Pharm. Bull. 17, 2377 (1969); Nagatsu et al., Biochem. Pharmacol. 19, 35 (1970). Toxicity study: Ishii et al., Arzneim.-Forsch. 25, 55 (1975).
Properties: Colorless crystals, mp 96-98°. LD50 orally in mice: 230 mg/kg (Ishii).
Melting point: mp 96-98°
Toxicity data: LD50 orally in mice: 230 mg/kg (Ishii)
 
Derivative Type: Copper salt
Properties: Bluish-violet crystals from water, mp 258-259°.
Melting point: mp 258-259°