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Key Documents

464929

Sigma-Aldrich

5-Hexenoic acid

98%

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About This Item

Linear Formula:
H2C=CH(CH2)3CO2H
CAS Number:
Molecular Weight:
114.14
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

refractive index

n20/D 1.435 (lit.)

bp

105 °C/15 mmHg (lit.)

density

0.961 g/mL at 25 °C (lit.)

SMILES string

OC(=O)CCCC=C

InChI

1S/C6H10O2/c1-2-3-4-5-6(7)8/h2H,1,3-5H2,(H,7,8)

InChI key

XUDOZULIAWNMIU-UHFFFAOYSA-N

Application

5-Hexenoic acid may be used for the preparation of iodolactone derivatives and fluorine-containing δ-valerolactones.

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

219.2 °F - closed cup

Flash Point(C)

104 °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’.

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Synthesis of fluoroalkyl-d-lactones from polyfluoroalkyl iodides and 5-hexenoic acids.
Fang X, et al.
Journal of Fluorine Chemistry, 129(4), 280-285 (2008)
Tertiary aminourea-catalyzed enantioselective iodolactonization.
Gemma E Veitch et al.
Angewandte Chemie (International ed. in English), 49(40), 7332-7335 (2010-08-31)
Stilianos G Roussis et al.
Journal of chromatography. A, 1594, 105-111 (2019-03-02)
In an effort to improve separation of impurities in oligonucleotide drugs, alkyl amines of different length and carbon content were evaluated as reagents in ion pair-reversed phase (IP-RP) HPLC with mass spectrometric detection. A range of columns was tested in
Philipp Höfer et al.
Microbial cell factories, 9, 70-70 (2010-09-18)
Methylotrophic (methanol-utilizing) bacteria offer great potential as cell factories in the production of numerous products from biomass-derived methanol. Bio-methanol is essentially a non-food substrate, an advantage over sugar-utilizing cell factories. Low-value products as well as fine chemicals and advanced materials

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