Skip to Content
Merck
All Photos(2)

Key Documents

193089

Sigma-Aldrich

trans-2-Hexenoic acid

99%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3CH2CH2CH=CHCO2H
CAS Number:
Molecular Weight:
114.14
Beilstein:
1720443
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

>1 (vs air)

Quality Level

Assay

99%

form

solid

refractive index

n20/D 1.438 (lit.)

bp

217 °C (lit.)

mp

33-35 °C (lit.)

density

0.965 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CCC\C=C\C(O)=O

InChI

1S/C6H10O2/c1-2-3-4-5-6(7)8/h4-5H,2-3H2,1H3,(H,7,8)/b5-4+

InChI key

NIONDZDPPYHYKY-SNAWJCMRSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible, corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Saloni Pasta et al.
Chemistry & biology, 14(12), 1377-1385 (2007-12-22)
Expression, characterization, and mutagenesis of a series of N-terminal fragments of an animal fatty acid synthase, containing the beta-ketoacyl synthase, acyl transferase, and dehydratase domains, demonstrate that the dehydratase domain consists of two pseudosubunits, derived from contiguous regions of the
Rhodium-catalyzed asymmetric 1, 4-addition of arylboron reagents to α,β-unsaturated esters.
Takaya Y, et al.
Tetrahedron Asymmetry, 10(20), 4047-4056 (1999)
Biooxidation of primary alcohols to aldehydes through hydrogen transfer employing janibacter terrae.
Orbegozo T, et al.
European Journal of Organic Chemistry, 2010(18), 3445-3448 (2010)
Fangfang Zeng et al.
Insect biochemistry and molecular biology, 113, 103213-103213 (2019-08-24)
Mosquitoes rely heavily on the olfactory system to find a host for a bloodmeal, plants for a source of energy and suitable sites for oviposition. Here, we examined a cluster of eight odorant receptors (ORs), which includes one OR, CquiOR1
Pingxi Xu et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(46), 16592-16597 (2014-10-29)
Insect repellents are important prophylactic tools for travelers and populations living in endemic areas of malaria, dengue, encephalitis, and other vector-borne diseases. DEET (N,N-diethyl-3-methylbenzamide) is a 6-decade-old synthetic repellent, which is still considered the gold standard of mosquito repellents. Mosquitoes

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service