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CAS No 7681-93-8 , Pimaricin Search by region : China

  • Name: Pimaricin
  • Synonyms: pimaricin approx. 2.5% aqueous*suspension gamma-I;Natamycin;Pimaricin; Natamycin; pimafucin (pimaricin in 2.5% sterile water suspen; Pimaricin, Streptomyces chattanoogensis (1.07360); Pimaricin;
  • CAS Registry Number:
  • Melting Point: 2000C (dec)
  • Density: 1.0 g/mL at 20 °C(lit.)
  • Refractive index: 1.62
  • Safety Statements: 24/25-36
  • Hazard Symbols: Xn: Harmful;
  • EINECS: 231-683-5
  • Molecular Weight: 665.73
  • InChI: InChI=1/C33H47NO13/c1-18-10-8-6-4-3-5-7-9-11-21(45-32-30(39)28(34)29(38)19(2)44-32)15-25-27(31(40)41)22(36)17-33(42,47-25)16-20(35)14-24-23(46-24)12-13-26(37)43-18/h3-9,11-13,18-25,27-30,32,35-36,38-39,42H,10,14-17,34H2,1-2H3,(H,40,41)/b4-3+,7-5+,8-6+,11-9+,13-12+/t18?,19?,20?,21?,22?,23?,24?,25?,27?,28-,29+,30-,32-,33?/m0/s1
  • Risk Statements: S24/25:Avoidcontactwithskinandeyes.;
  • Molecular Formula: C33H47NO13
  • Molecular Structure:CAS No:7681-93-8 Pimaricin

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    References of Pimaricin
    Title: Natamycin
    CAS Registry Number: 7681-93-8
    CAS Name: Pimaricin
    Synonyms: antibiotic A 5283; tennecetin
    Manufacturers' Codes: CL-12625
    Trademarks: Mycophyt (Mycofarm); Myprozine (Am. Cyanamid); Natacyn (Alcon); Pimafucin (Basotherm); Synogil (Basotherm)
    Molecular Formula: C33H47NO13
    Molecular Weight: 665.73
    Percent Composition: C 59.54%, H 7.12%, N 2.10%, O 31.24%
    Literature References: Polyene antifungal antibiotic produced by Streptomyces natalensis from soil near Pietermaritzburg, South Africa and by S. chattanoogensis. Isoln: Struyk et al., Antibiot. Annu. 1957-1958, 878. Prodn: GB 844289 (1960 to Koninklijke Nederlandsche Gist en Spiritus-Fabriek); GB 846933 (1960 to Am. Cyanamid). Identity with tennecetin: Divekar et al., Antibiot. Chemother. 11, 377 (1961). Structure: Golding et al., Tetrahedron Lett. 1966, 3551; Meyer, Chem. Commun. 1968, 470. Configuration: Gaudiano et al., Chim. Ind. (Milan) 48, 1327 (1966). Revised structure: R. C. Pandey, K. L. Rinehart, J. Antibiot. 29, 1035 (1976). Soly data: Marsh, Weiss, J. Assoc. Off. Anal. Chem. 50, 457 (1967). Toxicology: G. J. Levinskas et al., Toxicol. Appl. Pharmacol. 8, 97 (1966). Comprehensive description: H. Brik, Anal. Profiles Drug Subs. Excip. 23, 399-419 (1994).
    Properties: Crystals from methanol + water, darkens ~200°, dec 280-300°. [a]D20 +278° (c = 1 in CH3COOH). Sensitive to light, but otherwise very stable in the dry state. uv max (methanol + 0.1% CH3COOH): 220, 280, 290, 303, 318 nm (e 21300, 26630, 52930, 83220, 76230). Soly at 20° (g/ml): 87% glycerol 0.18. Practically insol in higher alcohols, ether, esters, aromatic or aliphatic hydrocarbons, chlorinated hydrocarbons, ketones, dioxane, cyclohexanol, oils. LD50 orally in male, female rats (g/kg): 2.73, 4.67 (Levinskas).
    Optical Rotation: [a]D20 +278° (c = 1 in CH3COOH)
    Absorption maximum: uv max (methanol + 0.1% CH3COOH): 220, 280, 290, 303, 318 nm (e 21300, 26630, 52930, 83220, 76230)
    Toxicity data: LD50 orally in male, female rats (g/kg): 2.73, 4.67 (Levinskas)
    Therap-Cat: Antifungal (topical).
    Keywords: Antifungal (Antibiotics); Polyenes.