ChemicalBook--->CAS DataBase List--->53448-07-0

53448-07-0

53448-07-0 Structure

53448-07-0 Structure
IdentificationMore
[Name]

TRANS-2-UNDECENAL
[CAS]

53448-07-0
[Synonyms]

2-UNDECEN-1-AL
2-UNDECENAL
FEMA 3423
TRANS-2-HENDECEN-1-AL
TRANS-2-UNDECEN-1-AL
TRANS-2-UNDECEN-1-YL ALDEHYDE
TRANS-2-UNDECENAL
(2E)-2-Undecenal
(E)-2-Undecanal
(E)-2-undecenal
(E)-undec-2-enal
2-Undecenal, (E)-
2-Undecenal, trans
trans Undec-2-enal
undec-2(E)-enal
ETHYL UNDECANOATE 97+%
(E)-2-undecenal,trans-2-undecenal,(2E)-2-undecenal
trans-2-Undecenal, 95%, remainder mainly cis-isomer
trans-2-Hendecenal
trans-2-Undecenyl aldehyde
[EINECS(EC#)]

219-564-6
[Molecular Formula]

C11H20O
[MDL Number]

MFCD00014680
[Molecular Weight]

168.28
[MOL File]

53448-07-0.mol
Chemical PropertiesBack Directory
[Melting point ]

115°
[Boiling point ]

115 °C10 mm Hg(lit.)
[density ]

0.849 g/mL at 25 °C(lit.)
[FEMA ]

3423 | 2-UNDECENAL
[refractive index ]

n20/D 1.457(lit.)
[Fp ]

>230 °F
[form ]

clear liquid
[color ]

Colorless to Light yellow
[Odor]

at 1.00 % in dipropylene glycol. fresh fruity citrus orange peel
[biological source]

synthetic
[Odor Type]

fruity
[BRN ]

1762239
[Major Application]

flavors and fragrances
[Cosmetics Ingredients Functions]

PERFUMING
[InChI]

1S/C11H20O/c1-2-3-4-5-6-7-8-9-10-11-12/h9-11H,2-8H2,1H3/b10-9+
[InChIKey]

PANBRUWVURLWGY-MDZDMXLPSA-N
[SMILES]

[H]C(=O)\C([H])=C(/[H])CCCCCCCC
[LogP]

4.23
[CAS DataBase Reference]

53448-07-0(CAS DataBase Reference)
[NIST Chemistry Reference]

2-Undecenal, e-(53448-07-0)
Safety DataBack Directory
[Hazard Codes ]

N
[Risk Statements ]

50/53
[Safety Statements ]

61
[RIDADR ]

UN 3082 9 / PGIII
[WGK Germany ]

3
[HS Code ]

2912.19.5000
[Storage Class]

10 - Combustible liquids
[Hazard Classifications]

Aquatic Acute 1
Hazard InformationBack Directory
[Uses]

flavors and fragrances
[Definition]

ChEBI: 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 Description]

trans-2-undecenal is mainly formed due to the oxidation of triolein while heating. It occurs naturally in coriander, fresh red pepper and watermelon.
Spectrum DetailBack Directory
[Spectrum Detail]

TRANS-2-UNDECENAL(53448-07-0)MS
TRANS-2-UNDECENAL(53448-07-0)13CNMR
TRANS-2-UNDECENAL(53448-07-0)IR1
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

trans-2-Undecenal, 95%, remainder mainly cis-isomer(53448-07-0)
[Sigma Aldrich]

53448-07-0(sigmaaldrich)
[TCI AMERICA]

trans-2-Undecenal,>93.0%(GC)(T)(53448-07-0)
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