Skip to Content
Merck
CN

193089

trans-2-Hexenoic acid

99%

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
CH3CH2CH2CH=CHCO2H
CAS Number:
Molecular Weight:
114.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
236-528-5
Beilstein/REAXYS Number:
1720443
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

trans-2-Hexenoic acid, 99%

InChI key

NIONDZDPPYHYKY-SNAWJCMRSA-N

InChI

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

SMILES string

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

vapor density

>1 (vs air)

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.)

functional group

carboxylic acid

storage temp.

2-8°C

Quality Level

Looking for similar products? Visit Product Comparison Guide

Related Categories

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

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

Visit the Document Library

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)
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)
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