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CAS No 533-87-9 , (±)-erythro-Aleuritic acid

  • CAS Registry Number:
  • Melting Point: 100-101 °C(lit.)
  • Density: 1.085 g/cm3
  • Refractive index: 1.498
  • Safety Statements: Poison by intravenous route. When heated to decomposition it emits acrid smoke and irritating fumes.
  • EINECS: 232-692-7
  • Molecular Weight: 304.42
  • InChI: InChI=1/C16H32O5/c17-13-9-5-4-7-11-15(19)14(18)10-6-2-1-3-8-12-16(20)21/h14-15,17-19H,1-13H2,(H,20,21)
  • Risk Statements: S24/25:Avoidcontactwithskinandeyes.;
  • Molecular Formula: C16H32O5
  • Molecular Structure:CAS No:533-87-9 (±)-erythro-Aleuritic acid
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533-87-9 Aleuritic acid

  • Aleuritic acid9,10,16-trihydroxypalmitic acid
  • United States INDOFINE Chemical Co., Inc. [Manufacturer]
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533-87-9 ALEURITIC ACID

  • ALEURITIC ACID, 95%
  • United States INTERNATIONAL LABORATORY LIMITED [Manufacturer]
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533-87-9 ALEURITIC ACID(RG)

  • ALEURITIC ACID(RG)9,10,16-Trihydroxypalmitic acid
  • United States ChromaDex Inc. [Manufacturer]
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533-87-9 Aleuritic Acid

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533-87-9 A12961 ALEURITIC ACID 90%

  • United States Pfaltz & Bauer [Manufacturer]
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533-87-9 (+/-)-ERYTHRO-ALEURITIC ACID 95%

  • United States International Laboratory (IL) [Manufacturer]
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533-87-9 ALEURITIC ACID

  • Germany Beckmann-Kenko GmbH [Manufacturer]
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533-87-9 (±)-erythro-Aleuritic acid

  • Germany Beckmann Chemikalien KG [Manufacturers]
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533-87-9 erythro-Aleuritic acid

  • erythro-Aleuritic acid
  • Germany ABCR GmbH & Co KG [Manufacturer]
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533-87-9 Aleuritic acid

  • Aleuritic acid
  • Germany CHEMOS GmbH [Manufacturer]
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References of (±)-erythro-Aleuritic acid
Title: Aleuritic Acid
CAS Registry Number: 533-87-9
CAS Name: (9R,10S)-rel-9,10,16-Trihydroxyhexadecanoic acid
Synonyms: 9,10,16-trihydroxypalmitic acid; 8,9,15-trihydroxypentadecane-1-carboxylic acid
Molecular Formula: C16H32O5
Molecular Weight: 304.42
Percent Composition: C 63.13%, H 10.60%, O 26.28%
Literature References: One of the constituent acids of shellac. Obtained in 43% yield from dewaxed shellac: Schaeffer, Gardner, Ind. Eng. Chem. 30, 333 (1938); Gidvani, J. Chem. Soc. 1944, 306; Sengupta, Bose, J. Sci. Ind. Res. 11B, 458 (1952). The acid obtained from shellac is optically inactive, although it contains two asymmetric carbon atoms. It has been shown to be the DL-erythro or dl-cis form, and is the only form described here. Synthesis of diastereoisomers: Mitter et al., Sci. Cult. 8, 273 (1942); Hunsdiecker, Ber. 76, 142 (1943); 77, 185 (1944); Baudart, Compt. Rend. 221, 205 (1945).
Properties: Crystals from dilute ethanol, mp 100-101°. Sol in methanol. Forms a crystalline sodium salt.
Melting point: mp 100-101°
 
Derivative Type: Methyl ester
Molecular Formula: C17H34O5
Molecular Weight: 318.45
Percent Composition: C 64.12%, H 10.76%, O 25.12%
Properties: Fine feathery needles, mp 72-73°; bp0.1 235°. Sol in methanol, ethanol, chloroform, acetone. Less sol in benzene. Insol in petr ether.
Melting point: mp 72-73°
Boiling point: bp0.1 235°
 
Derivative Type: Ethyl ester
CAS Registry Number: 6003-09-4
Molecular Formula: C18H36O5
Molecular Weight: 332.48
Percent Composition: C 65.02%, H 10.91%, O 24.06%
Properties: Needles from dil ethanol, mp 59°.
Melting point: mp 59°
 
Derivative Type: Hydrazide
CAS Registry Number: 6003-10-7
Molecular Formula: C16H34N2O4
Molecular Weight: 318.45
Percent Composition: C 60.35%, H 10.76%, N 8.80%, O 20.10%
Properties: Crystals from abs ethanol, mp 139-140°.
Melting point: mp 139-140°