Trans-?2-?Hexenal

Available forms:clear colorless to light yellow liquid

pd_proNo:437258-e7bbdb83-8df6-4032-ba34-f72b860e9584

pd_productuse:

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Detailed introduction

Chinese Manufacturer Supply Trans-?2-?Hexenal 6728-26-3 On Stock with Competitive Price

  • Molecular Formula:C6H10O
  • Molecular Weight:98.1448
  • Appearance/Colour:clear colorless to light yellow liquid 
  • Vapor Pressure:10 mm Hg ( 20 °C) 
  • Melting Point:-78°C (estimate) 
  • Refractive Index:n20/D 1.446(lit.)  
  • Boiling Point:146.499 °C at 760 mmHg 
  • Flash Point:38.333 °C 
  • PSA:17.07000 
  • Density:0.828 g/cm3 
  • LogP:1.54160 

TRANS-2-HEXENAL(Cas 6728-26-3) Usage

Descriptioin

Tans-2-Hexenal is a colorless to pale yellow clear liquid. It occurs naturally in tomatoes, banana and black tea. It gives a leafy, fruity, fatty, apple banana, strawberry note.1 It is mostly used as a flavoring agent in food. It is also used in air care products, cleaning and furnishing care products, laundry and dishwashing products.

Synthesis Reference(s)

Journal of the American Chemical Society, 71, p. 3468, 1949 DOI: 10.1021/ja01178a061Tetrahedron Letters, 36, p. 8513, 1995 DOI: 10.1016/0040-4039(95)01784-F

Definition

ChEBI: A 2-hexenal in which the olefinic double bond has E configuration. It occurs naturally in a wide range of fruits, vegetables, and spices.

General Description

trans-2-Hexen-1-al is an important flavoring compound that occurs naturally in tomatoes, banana and black tea.

InChI:InChI=1/C6H10O/c1-2-3-4-5-6-7/h4-6H,2-3H2,1H3/b5-4+

6728-26-3 Relevant articles

Efficient Aerobic Oxidation of trans-2-Hexen-1-ol using the Aryl Alcohol Oxidase from Pleurotus eryngii

de Almeida,van Schie,Ma,Tieves,Younes,Fernández-Fueyo,Arends,Riul,Hollmann

, p. 2668 - 2672 (2019)

The selective oxidation of trans-2-hexen...

EFFICIENT INDIRECT ELECTROCHEMICAL IN SITU REGENERATION OF NAD+ AND NADP+ FOR ENZYMATIC OXIDATIONS USING IRON BIPYRIDINE AND PHENANTHROLINE COMPLEXES AS REDOX CATALYSTS

Komoschinski, Joachim,Steckhan, Eberhard

, p. 3299 - 3300 (1988)

Using iron bipyridine or phenanthroline ...

Biocatalytic synthesis of the Green Note trans-2-hexenal in a continuous-flow microreactor

Van Schie, Morten M.C.H.,De Almeida, Tiago Pedroso,Laudadio, Gabriele,Tieves, Florian,Fernández-Fueyo, Elena,No?l, Timothy,Arends, Isabel W.C.E.,Hollmann, Frank

, p. 697 - 703 (2018)

The biocatalytic preparation of trans-he...

Characterization of a new (Z)-3:(E)-2-hexenal isomerase from tea (Camellia sinensis) involved in the conversion of (Z)-3-hexenal to (E)-2-hexenal

Chen, Cong,Chen, Shuna,He, Puming,Li, Bo,Tu, Youying,Wang, Feiquan,Wang, Kaixi,Wen, Xinli,Wu, Yuanyuan,Yu, Fei,Zhang, Jianming

, (2022/03/14)

Two major green leaf volatiles (GLVs) in...

Synthesis and Biological Evaluation of Hoshionolactam-Based Compounds

Elizebath, Drishya,Jachak, Gorakhnath R.,Reddy, D. Srinivasa,Shanmugam, Dhanasekaran,Shukla, Anurag

, p. 2212 - 2218 (2021/07/22)

In search of novel antitrypanosomal agen...

Biosynthesis of Mycotoxin Fusaric Acid and Application of a PLP-Dependent Enzyme for Chemoenzymatic Synthesis of Substituted l -Pipecolic Acids

Hai, Yang,Chen, Mengbin,Huang, Arthur,Tang, Yi

supporting information, p. 19668 - 19677 (2020/12/01)

Fusaric acid (FA) is a well-known mycoto...

First synthesis of 3-S-glutathionylhexanal-d8 and its bisulfite adduct

Muhl, Jennifer R.,Pilkington, Lisa I.,Deed, Rebecca C.

supporting information, (2020/06/17)

3-Sulfanylhexan-1-ol (3SH) is an impact ...

6728-26-3 Process route

(Z)-3-Hexen-1-ol
928-96-1

(Z)-3-Hexen-1-ol

sulfuric acid
7664-93-9

sulfuric acid

(E)-2-Hexenal
6728-26-3

(E)-2-Hexenal

(E)-2-Hexenoic acid
13419-69-7

(E)-2-Hexenoic acid

Conditions
Conditions Yield
(E)-2-Hexen-1-ol
928-95-0

(E)-2-Hexen-1-ol

(E)-2-Hexenal
6728-26-3

(E)-2-Hexenal

(E)-2-Hexenoic acid
13419-69-7

(E)-2-Hexenoic acid

Conditions
Conditions Yield
With C21H22N2O2Pd; oxygen; In toluene; at 100 ℃; for 12h; under 3000.3 Torr; Reagent/catalyst;

6728-26-3 Upstream products

  • 928-96-1
    928-96-1

    (Z)-3-Hexen-1-ol

  • 101-33-7
    101-33-7

    1,1,3-triethoxy-hexane

  • 101713-97-7
    101713-97-7

    1-ethoxy-hex-3-en-2-ol

  • 28998-62-1
    28998-62-1

    1,1-dimethoxyhexane-3-one

6728-26-3 Downstream products

  • 22329-75-5
    22329-75-5

    (2E,4E)-octadienoic acid

  • 67077-39-8
    67077-39-8

    trans-3-hepten-2-ol

  • 102178-95-0
    102178-95-0

    hex-2t-enal-[4-(4-phenylazo-phenyl)-semicarbazone]

  • 928-95-0
    928-95-0

    (E)-2-Hexen-1-ol

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