Docosanamide

Suppliers

Names

[ CAS No. ]:
3061-75-4

[ Name ]:
Docosanamide

[Synonym ]:
docosanamid
MFCD00047905
ACMC-209hhe
Docosanylamide
Behenamide
Behenic acid amide
Amide C22
Docosansaeureamid
AC1L2QZB
Behenic amide
Behenylamide
Docosanamide
EINECS 221-304-1

Chemical & Physical Properties

[ Density]:
0.9±0.1 g/cm3

[ Boiling Point ]:
471.1±13.0 °C at 760 mmHg

[ Melting Point ]:
110-113 °C

[ Molecular Formula ]:
C22H45NO

[ Molecular Weight ]:
339.599

[ Flash Point ]:
238.7±19.8 °C

[ Exact Mass ]:
339.350128

[ PSA ]:
43.09000

[ LogP ]:
9.39

[ Vapour Pressure ]:
0.0±1.2 mmHg at 25°C

[ Index of Refraction ]:
1.460

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
1

[ HS Code ]:
2924199090

Synthetic Route

Precursor & DownStream

Precursor

  • Docosanoic acid
  • behenoyl chloride

DownStream

Customs

[ HS Code ]: 2924199090

[ Summary ]:
2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Use of reversed phase HP liquid chromatography to assay conversion of N-acylglycines to primary fatty acid amides by peptidylglycine-alpha-amidating monooxygenase.

J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 809(1) , 15-21, (2004)

Primary fatty acid amides (R-CO-NH2) and N-acylglycines (R-CO-NH-CH2-COOH) are classes of compounds that have only recently been isolated and characterized from biological sources. Key questions remai...


More Articles


Related Compounds

  • N-phenyldocosanamide
  • N-docosyldocosanamide
  • N-octadecyldocosanamide
  • N,N-dimethyldocosanamide
  • N,N'-Methylenedidocosanamide
  • N-hydroxymethyl-docosanamide
  • N-(2-(4-(isopropylamino)-6-(methylthio)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)thiophene-2-carboxamide
  • 1-ethyl-2-(tetrahydrofuran-2-yl)-1H-benzo[d]imidazole hydrochloride
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • 5-Bromo-4-(bromomethyl)thiazole
  • Diethyl Chlorophosphate-d10
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide