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153745

Sigma-Aldrich

Hexanoic acid

≥99%

Sinonimo/i:

Acid C6, Caproic acid

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About This Item

Formula condensata:
CH3(CH2)4COOH
Numero CAS:
142-62-1
Peso molecolare:
116.16
Beilstein:
773837
Numero CE:
205-550-7
Numero MDL:
MFCD00004421
Codice UNSPSC:
12352100
ID PubChem:
24849370
NACRES:
NA.22

Densità del vapore

4 (vs air)

Tensione di vapore

0.18 mmHg ( 20 °C)

Saggio

≥99%

Stato

liquid

Indice di rifrazione

n20/D 1.4161 (lit.)

P. ebollizione

202-203 °C (lit.)

Punto di fusione

−4 °C (lit.)

Solubilità

H2O: slightly soluble
diethyl ether: easily soluble
ethanol: easily soluble

Densità

0.927 g/mL at 25 °C (lit.)

Gruppo funzionale

carboxylic acid

Organolettico

pungent

Stringa SMILE

CCCCCC(O)=O

InChI

1S/C6H12O2/c1-2-3-4-5-6(7)8/h2-5H2,1H3,(H,7,8)
FUZZWVXGSFPDMH-UHFFFAOYSA-N

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Descrizione generale

Hexanoic acid is a resistance priming inducer that protects tomato plants from Botrytis cinerea.

Applicazioni

Hexanoic acid can be used:
  • To prepare polyethylene glycol derived nanomicelles as a non-viral gene carrier.
  • As a starting material to synthesize an amino acid L-norleucine.
  • As a reactant to prepare 4-methoxy phenyl hexyl ketone through Friedel−Crafts acylation of anisole using Hβ zeolite-based catalyst.
  • As a template in the preparation of highly conducting thin polypyrrole coated alumina composite particles.

Pittogrammi

Corrosion
GHS05

Avvertenze

Danger

Indicazioni di pericolo

H314

Classi di pericolo

Eye Dam. 1 - Skin Corr. 1C

Codice della classe di stoccaggio

8A - Combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

215.6 °F - closed cup

Punto d’infiammabilità (°C)

102 °C - closed cup

Dispositivi di protezione individuale

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificati d'analisi (COA)

Lot/Batch Number
MKCP8918
MKCN0134
MKCL9018
MKCK8826
MKCH9032

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Sigma-Aldrich

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4-Methylvaleric acid 99%

Sigma-Aldrich

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Octanoic acid ≥98%

Sigma-Aldrich

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Isovaleric acid 99%

Sigma-Aldrich

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Sigma-Aldrich

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Ivan Finiti et al.
Molecular plant pathology, 15(6), 550-562 (2013-12-11)
Treatment with the resistance priming inducer hexanoic acid (Hx) protects tomato plants from Botrytis cinerea by activating defence responses. To investigate the molecular mechanisms underlying hexanoic acid-induced resistance (Hx-IR), we compared the expression profiles of three different conditions: Botrytis-infected plants
Buddhadev Layek et al.
Molecular pharmaceutics, 11(3), 982-994 (2014-02-07)
Gene therapy holds immense potential as a future therapeutic strategy for the treatment of numerous genetic diseases which are incurable to date. Nevertheless, safe and efficient gene delivery remains the most challenging aspects of gene therapy. To overcome this difficulty
Enantioselective biocatalytic formal α-amination of hexanoic acid to l-norleucine
Dennig A, et al.
Organic & Biomolecular Chemistry, 16(43), 8030-8033 (2018)
Formation of ultrathin polypyrrole (PPY) films on alumina particles using adsorbed hexanoic acid as a template.
Cho G, et al.
Langmuir, 16(10), 4424-4429 (2000)
Diya Alsafadi et al.
New biotechnology, 34, 47-53 (2016-05-26)
Olive mill wastewater (OMW), a highly polluting waste from the olive oil industry, was utilized as sole carbon source for the production of polyhydroxyalkanoate (PHA) by extremely halophilic Haloferax Mediterranei (H. mediterranei) in a one stage cultivation step. H. mediterranei
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In this study, SPME was used for the analysis of free fatty acids in Parmesan cheese using a 65 μm Carbowax/divinylbenzene (DVB) SPME fiber. Headspace extraction of the cheese sample was conducted at 65 °C for 15 minutes and analyzed by GC with FID detection. SPME is ideal for analyzing the volatiles associated with solid food samples. The phase chemistry of the Nukol GC column provides excellent peak shape of acidic compounds.

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