Lauroyl alanine

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Names

[ CAS No. ]:
52558-74-4

[ Name ]:
Lauroyl alanine

[Synonym ]:
N-n-dodecanoyl (L)-alanine
Lauroylalanine
Lauryl-d-alanin
N-n-Dodecanoyl-(S)-alanine
L-Alanine,N-(1-oxododecyl)
N-Lauroyl-L-alanin

Chemical & Physical Properties

[ Density]:
0.979g/cm3

[ Boiling Point ]:
452.1ºC at 760mmHg

[ Melting Point ]:
83 °C

[ Molecular Formula ]:
C15H29NO3

[ Molecular Weight ]:
271.39600

[ Flash Point ]:
227.2ºC

[ Exact Mass ]:
271.21500

[ PSA ]:
66.40000

[ LogP ]:
3.88750

[ Storage condition ]:
2-8°C

MSDS

Safety Information

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

[ Safety Phrases ]:
22-24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2924199090

Synthetic Route

Precursor & DownStream

Precursor

  • Dodecanoyl chloride
  • L-alanine
  • Lauric acid
  • D-alanine
  • p-Nitrophenyl n-dodecanoyl L-alaninat

DownStream

  • L-alanine

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

A novel, simple method to simulate gelling process of injectable biodegradable in situ forming drug delivery system based on determination of electrical conductivity.

Int. J. Pharm. 404 , 176-179, (2011)

The purpose of the present study was to develop a novel, simple and determination-of-electrical-conductivity-based method to trace the gelling process of injectable biodegradable in situ forming organ...

Physical gelation of binary mixtures of hydrocarbons mediated by n-lauroyl-L-alanine and characterization of their thermal and mechanical properties. Bhattacharya S, Pal A.

J. Phys. Chem. B 112 , 491804927, (2998)


More Articles


Related Compounds

  • N-lauroyl alanine ethyl ester
  • LAUROYL BETA-ALANINE
  • lauroyl-thiourea
  • Lauroyl/Myristoyl Methyl Glucamide
  • Lauroyl azide
  • Lauroyl lactylate
  • 1-[(3-Aminocyclopentyl)methyl]-3-(3-methylbutan-2-yl)urea
  • 2-[Benzyl({[2-(propan-2-yl)phenyl]methyl})amino]ethan-1-ol
  • 2-[Butyl({[2-(propan-2-yl)phenyl]methyl})amino]ethan-1-ol
  • (1-{[2-(Propan-2-yl)phenyl]methyl}piperidin-4-yl)methanol
  • {2,2-Difluoro-3-[(3-methylbutan-2-yl)oxy]propyl}(ethyl)amine
  • 1-[Methyl({[2-(propan-2-yl)phenyl]methyl})amino]propan-2-ol
  • 5-Tert-butyl-3-methyl-1,2-oxazole-4-carbaldehyde
  • 3-Methyl-5-(propan-2-yl)-1,2-oxazole-4-carbaldehyde
  • 5-Tert-butyl-3-ethyl-1,2-oxazole-4-carbaldehyde
  • 5-Tert-butyl-3-(propan-2-yl)-1,2-oxazole-4-carbaldehyde
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