δ-Tridecalactone

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Names

[ CAS No. ]:
7370-92-5

[ Name ]:
δ-Tridecalactone

[Synonym ]:
2H-Pyran-2-one,tetrahydro-6-octyl
6-Octyltetrahydro-2H-pyran-2-one
5-tridecanolide
5-Hydroxytridecanoic acid lactone
delta-Tridecanolactone
TRIDECANO-1,5-LACTONE
δ-Tridecanolactone
tetrahydro-6-octyl-2h-pyran-2-on
δ-Tridecalactone
2H-Pyran-2-one, tetrahydro-6-octyl-
6-octyl-tetrahydro-pyran-2-one
Tetrahydro-6-octyl-2H-pyran-2-one
tridecanolactone

Chemical & Physical Properties

[ Density]:
0.9±0.1 g/cm3

[ Boiling Point ]:
309.1±10.0 °C at 760 mmHg

[ Molecular Formula ]:
C13H24O2

[ Molecular Weight ]:
212.329

[ Flash Point ]:
126.5±16.4 °C

[ Exact Mass ]:
212.177628

[ PSA ]:
26.30000

[ LogP ]:
4.01

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
1.450

MSDS

Safety Information

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2932999099

Synthetic Route

Precursor & DownStream

Precursor

  • 5-octyl-5-oxopentanal
  • 2-octylcyclopentan-1-one
  • 1-octyl-cyclopentene
  • Cyclopentanone

DownStream

Customs

[ HS Code ]: 2932999099

[ Summary ]:
2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Preparation of Optically Active δ-Tri- and δ-Tetradecalactones by a Combination of Novozym 435-catalyzed Enantioselective Methanolysis and Amidation.

J. Oleo Sci. 64(11) , 1213-26, (2015)

A combination of Novozym 435-catalyzed methanolysis and amidation using racemic N-methyl-5-acetoxytridecan- and tetradecanamides as a substrate proceeded in good enantioselectivity to afford the corre...

Two distinct pathways for the formation of hydroxy FA from linoleic acid by lactic acid bacteria.

Lipids 38(12) , 1269-74, (2003)

Twenty-three of 86 strains of lactic acid bacteria transformed linoleic acid into hydroxy FA. Two distinct conversion pathways were in operation. Two strains of Lactobacillus acidophilus and a strain ...


More Articles


Related Compounds

  • (R)-δ-tridecalactone
  • δ-thiol-Nε-(p-nitrocarbobenzyloxy)lysine 2,2,2-trifluoroacetate
  • δ-Diethylamino-α-phenylvalerophenone
  • δ-MSH
  • Δ-tris(1,10-phenanthroline)ruthenium(2+)
  • δ-oxy-δ-(2.5-dimethyl-phenyl)-α-amylene
  • 4-(7-Chloro-6-(4-chlorophenyl)quinazolin-4-yl)piperazine-2-carboxamide
  • 6-Amino-4-bromo-3-chloro-2-fluorobenzoic acid
  • N-(3-Bromo-4-chlorobenzyl)-2,2-diethoxy-N-tosylethanamine
  • 7-Bromo-6-chlorocinnolin-4-ol
  • 6-Bromo-4,7-dichloro-2-methylquinazoline
  • Ethyl 7-bromo-6-chloro-8-fluoro-4-hydroxyquinoline-3-carboxylate
  • 1-[4-[7-Chloro-6-(2-chlorophenyl)-4-quinazolinyl]-1-piperazinyl]-2-propen-1-one
  • 6-Chloro-5-(2-chlorophenyl)-N-4-piperidinyl-1h-indazol-3-amine
  • 1-Acryloyl-4-(6-chloroisoquinolin-1-yl)piperazine-2-carboxamide
  • 7-Chloro-6-(4-chlorophenyl)-4-hydroxy-3-quinolinecarbonitrile
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