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CAS No 94421-68-8 , (5Z,8Z,11Z,14Z)-N-(2-hydroxyethyl)icosa-5,8,11,14-tetraenamide Search by region : Germany

  • Name: (5Z,8Z,11Z,14Z)-N-(2-hydroxyethyl)icosa-5,8,11,14-tetraenamide
  • Synonyms: (5Z,8Z,11Z,14Z)-N-(2-hydroxyethyl)icosa-5,8,11,14-tetraenamide;Arachidonylethanolamide; N-Arachidonoyl-2-hydroxyethylamide; 5,8,11,14-Eicosatetraenoylethanolamide; Arachidonoyl ethanolamide;
  • CAS Registry Number:
  • Transport: UN 1170 3
  • Flash Point: 269.7 ºC
  • Boiling Point: 522.3 ºCat 760 mmHg
  • Refractive index: 1.503
  • Safety Statements: 24/25-16-7
  • Hazard Symbols: F: Flammable;
  • Flash Point: 269.7 ºC
  • Molecular Weight: 347.53468
  • InchiKey: LGEQQWMQCRIYKG-DOFZRALJSA-N
  • InChI: InChI=1S/C22H37NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22
    (25)23-20-21-24/h6-7,9-10,12-13,15-16,24H,2-5,8,11,14,17-21H2,1H3,(H,23,
    25)/b7-6-,10-9-,13-12-,16-15-
  • Risk Statements: 11
  • Molecular Formula: C22H37NO2
  • Molecular Structure:CAS No:94421-68-8 (5Z,8Z,11Z,14Z)-N-(2-hydroxyethyl)icosa-5,8,11,14-tetraenamide

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  • 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
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94421-68-8 5,8,11,14-Eicosatetraenamide,N-(2-hydroxyethyl)-, (5Z,8Z,11Z,14Z)-

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94421-68-8 Anandamide (in TocrisolveTM 100)

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References of (5Z,8Z,11Z,14Z)-N-(2-hydroxyethyl)icosa-5,8,11,14-tetraenamide
Title: Anandamide
CAS Registry Number: 94421-68-8
CAS Name: (5Z,8Z,11Z,14Z)-N-(2-Hydroxyethyl)-5,8,11,14-eicosatetraenamide
Synonyms: arachidonylethanolamide; N-(2-hydroxyethyl)arachidonamide
Molecular Formula: C22H37NO2
Molecular Weight: 347.53
Percent Composition: C 76.03%, H 10.73%, N 4.03%, O 9.21%
Literature References: Endogenous ligand for the mammalian cannabinoid receptor; derivative of arachidonic acid, q.v. Name coined from the Sanskrit word "ananda," meaning bliss. Identification in pig brain: W. A. Devane et al., Science 258, 1946 (1992). Identification in chocolate and cocoa: E. di Tomaso et al., Nature 382, 677 (1996). Pharmacology: P. B. Smith et al., J. Pharmacol. Exp. Ther. 270, 219 (1994). Biosynthetic studies: W. A. Devane, J. Axelrod, Proc. Natl. Acad. Sci. USA 91, 6698 (1994); V. Di Marzo et al., Nature 372, 686 (1994). LC/MS/MS determn and distribution in human tissues: C. C. Felder et al., FEBS Lett. 393, 231 (1996). Review: V. Di Marzo, A. Fontana, Prostaglandins Leukotrienes Essent. Fatty Acids 53, 1-11 (1995).