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Merck

538701

Sigma-Aldrich

2-Ethylhexanoic acid

≥99%

Sinónimos:

2-Ethylcaproic acid

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About This Item

Fórmula lineal:
CH3(CH2)3CH(C2H5)CO2H
Número de CAS:
Peso molecular:
144.21
Beilstein:
1750468
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
NACRES:
NA.22

densidad de vapor

4.98 (vs air)

Nivel de calidad

presión de vapor

<0.01 mmHg ( 20 °C)
10 mmHg ( 115 °C)

Ensayo

≥99%

temp. de autoignición

699 °F

lim. expl.

1.04 %, 135 °F
8.64 %, 188 °F

índice de refracción

n20/D 1.425 (lit.)

bp

228 °C (lit.)

densidad

0.903 g/mL at 25 °C (lit.)

grupo funcional

carboxylic acid

cadena SMILES

CCCCC(CC)C(O)=O

InChI

1S/C8H16O2/c1-3-5-6-7(4-2)8(9)10/h7H,3-6H2,1-2H3,(H,9,10)

Clave InChI

OBETXYAYXDNJHR-UHFFFAOYSA-N

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Descripción general

2-Ethylhexanoic acid (EHXA, 2-EHA) is an industrially important aliphatic carboxylic acid. It is widely employed as a stabilizer and a wood preservative.
It has various industrial applications, such as:
  • coolant in automotives
  • synthetic lubricant
  • wetting agent
  • co-solvent
  • drying of paints
  • defoaming agent in pesticides

Aplicación

  • A review of the environmental fate and aquatic effects of a series of C4 and C8 oxo-process chemicals.: This review assesses the environmental impact of C4 and C8 oxo-process chemicals, including 2-Ethylhexanoic acid, detailing their degradation, persistence, and effects on aquatic ecosystems (Staples, 2001).

Pictogramas

Health hazard

Palabra de señalización

Danger

Frases de peligro

Clasificaciones de peligro

Repr. 1B

Código de clase de almacenamiento

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

237.2 °F - closed cup

Punto de inflamabilidad (°C)

114 °C - closed cup

Equipo de protección personal

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


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Visite la Librería de documentos

Synthetic applications of 2-ethylhexanoic acid derived reagents.
Raju R and Prasad K.
Tetrahedron, 68(5), 1341-1349 (2012)
The developmental toxicity of 2-ethylhexanoic acid in Wistar rats.
Pennanen S, et al.
Fundamental and Applied Toxicology, 19(4), 505-511 (1992)
Elizabeth Grillo Fernandes et al.
Biomacromolecules, 5(4), 1200-1205 (2004-07-13)
The increasing effort on development of bio-based polymeric materials in recent years is motivated by the basic concept of meeting the sustainability criteria for industrial development in the third millennium. Within this framework, our research group is currently involved in
I Svechnikova et al.
The Journal of endocrinology, 194(3), 603-609 (2007-09-01)
Phthalate esters are known to exert harmful effects on mammalian reproduction and fertility, but their potential adverse effects on the hormonal functions of the ovary have not yet been elucidated in detail. Here, we investigated the effects of di-(2-ethylhexyl) phthalate
H G Wahl et al.
Journal of chromatography. B, Biomedical sciences and applications, 758(2), 213-219 (2001-08-07)
A gas chromatographic-mass spectrometric method was developed for the quantitative analysis of the three Di(2-ethylhexyl)phthalate (DEHP) metabolites, 2-ethylhexanoic acid, 2-ethyl-3-hydroxyhexanoic acid and 2-ethyl-3-oxohexanoic acid in urine. After oximation with O-(2,3,4,5,6-pentafluorobenzyl)-hydroxylamine hydrochloride and sample clean-up with Chromosorb P filled glass tubes

Protocolos

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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