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trans-Hex-2-enoic acid

Names

[ CAS No. ]:
13419-69-7

[ Name ]:
trans-Hex-2-enoic acid

[Synonym ]:
MFCD00002705
FEMA 3169
2-trans-n-hexenoic acid
trans-2-Hexenoic acid
trans-2-hexenic acid
2-hexenoic acid
Z-hexenoic acid
FEMA NUMBER 3169
2-Hexenoic acid, (2E)-
(2E)-2-Hexenoic acid
ISOHYDROSORBIC ACID
EINECS 236-528-5
(2E)-Hex-2-enoic acid
T2 HEXENOIC ACID

Biological Activity

[Description]:

trans-Hex-2-enoic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
216.5±0.0 °C at 760 mmHg

[ Melting Point ]:
33-35 °C(lit.)

[ Molecular Formula ]:
C6H10O2

[ Molecular Weight ]:
114.142

[ Flash Point ]:
115.4±9.6 °C

[ Exact Mass ]:
114.068077

[ PSA ]:
37.30000

[ LogP ]:
1.87

[ Vapour density ]:
>1 (vs air)

[ Vapour Pressure ]:
0.1±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.456

[ Storage condition ]:
2-8°C

MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges

[ Hazard Codes ]:
C: Corrosive;

[ Risk Phrases ]:
R34

[ Safety Phrases ]:
S26-S36/37/39-S45-S25

[ RIDADR ]:
UN 2829 8/PG 3

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
8

[ HS Code ]:
2916190090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2916190090

[ Summary ]:
2916190090 unsaturated acyclic monocarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives。supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward)。VAT:17.0%。tax rebate rate:9.0%。MFN tariff:6.5%。general tariff:30.0%

Articles

Mosquito odorant receptor for DEET and methyl jasmonate.

Proc. Natl. Acad. Sci. U. S. A. 111(46) , 16592-7, (2014)

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-methylbe...

Rhodium-catalyzed asymmetric 1, 4-addition of arylboron reagents to α,β-unsaturated esters. Takaya Y, et al.

Tetrahedron Asymmetry 10(20) , 4047-56, (1999)

Biooxidation of primary alcohols to aldehydes through hydrogen transfer employing janibacter terrae. Orbegozo T, et al.

European J. Org. Chem. 2010(18) , 3445-48, (2010)


More Articles


Related Compounds

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