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TRANS-2-UNDECENAL

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CAS:53448-07-0
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CAS:53448-07-0
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TRANS-2-UNDECENAL manufacturers

  • TRANS-2-UNDECENAL
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  • 2025-06-27
  • CAS:53448-07-0
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 500000kg
  • TRANS-2-UNDECENAL
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  • $45.00
  • 2025-05-23
  • CAS:53448-07-0
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 20 tons
  • TRANS-2-UNDECENAL
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  • $8.50
  • 2025-02-13
  • CAS:53448-07-0
  • Min. Order: 1kg
  • Purity: 99.99%
  • Supply Ability: 10 tons
TRANS-2-UNDECENAL Basic information
Product Name:TRANS-2-UNDECENAL
Synonyms:TRANS-2-UNDECEN-1-AL;TRANS-2-UNDECEN-1-YL ALDEHYDE;TRANS-2-UNDECENAL;TRANS-2-HENDECEN-1-AL;(2E)-2-Undecenal;(E)-2-Undecanal;2-Undecenal, (E)-;2-Undecenal, trans
CAS:53448-07-0
MF:C11H20O
MW:168.28
EINECS:258-559-3
Product Categories:Alphabetical Listings;Flavors and Fragrances;Q-Z
Mol File:53448-07-0.mol
TRANS-2-UNDECENAL Structure
TRANS-2-UNDECENAL Chemical Properties
Melting point 115°
Boiling point 115 °C10 mm Hg(lit.)
density 0.849 g/mL at 25 °C(lit.)
refractive index n20/D 1.457(lit.)
FEMA 3423 | 2-UNDECENAL
Fp >230 °F
form clear liquid
color Colorless to Light yellow
Odorat 1.00 % in dipropylene glycol. fresh fruity citrus orange peel
Odor Typefruity
biological sourcesynthetic
BRN 1762239
Major Applicationflavors and fragrances
Cosmetics Ingredients FunctionsPERFUMING
InChI1S/C11H20O/c1-2-3-4-5-6-7-8-9-10-11-12/h9-11H,2-8H2,1H3/b10-9+
InChIKeyPANBRUWVURLWGY-MDZDMXLPSA-N
SMILES[H]C(=O)\C([H])=C(/[H])CCCCCCCC
LogP4.23
CAS DataBase Reference53448-07-0(CAS DataBase Reference)
NIST Chemistry Reference2-Undecenal, e-(53448-07-0)
Safety Information
Hazard Codes N
Risk Statements 50/53
Safety Statements 61
RIDADR UN 3082 9 / PGIII
WGK Germany 3
HS Code 2912.19.5000
Storage Class10 - Combustible liquids
Hazard ClassificationsAquatic Acute 1
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
TRANS-2-UNDECENAL Usage And Synthesis
Usesflavors and fragrances
DefinitionChEBI: A 2-undecenal in which the C2C bond has E configuration.
Synthesis Reference(s)The Journal of Organic Chemistry, 52, p. 3558, 1987 DOI: 10.1021/jo00392a011
Tetrahedron Letters, 16, p. 1007, 1975 DOI: 10.1016/S0040-4039(00)72629-3
General Descriptiontrans-2-undecenal is mainly formed due to the oxidation of triolein while heating. It occurs naturally in coriander, fresh red pepper and watermelon.
Tag:TRANS-2-UNDECENAL(53448-07-0) Related Product Information
TRANS-2-TRIDECEN-1-OL 97 TRANS-2-OCTENE trans-2-Octen-1-ol TRANS-2-PENTENOIC ACID trans-2-Pentene TRANS-2-PHENYL-1-CYCLOPROPANECARBOXYLIC ACID ZINC TELLURIDE 10-UNDECENAL TRANS-2-UNDECENAL 10-Undecenal ADOXAL 2-Undecenal ETHYL UNDECANOATE Undecanal CIS-8-UNDECENAL,8-Undecena 6,10-DIMETHYL-3-OXA-9-UNDECENAL CIS-8-UNDECENAL