Skip to Content
Merck

538701

2-Ethylhexanoic acid

≥99%

Synonym(s):

2-Ethylcaproic acid

Sign In to View Organizational & Contract Pricing.

Select a Size



About This Item

Linear Formula:
CH3(CH2)3CH(C2H5)CO2H
CAS Number:
Molecular Weight:
144.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-743-6
Beilstein/REAXYS Number:
1750468
MDL number:

Product Name

2-Ethylhexanoic acid, ≥99%

InChI key

OBETXYAYXDNJHR-UHFFFAOYSA-N

InChI

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

SMILES string

CCCCC(CC)C(O)=O

vapor density

4.98 (vs air)

vapor pressure

<0.01 mmHg ( 20 °C)
10 mmHg ( 115 °C)

assay

≥99%

autoignition temp.

699 °F

expl. lim.

1.04 %, 135 °F
8.64 %, 188 °F

refractive index

n20/D 1.425 (lit.)

bp

228 °C (lit.)

density

0.903 g/mL at 25 °C (lit.)

functional group

carboxylic acid

Quality Level

Looking for similar products? Visit Product Comparison Guide

Application

  • 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).

General description

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

pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Repr. 1B

Storage Class

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

wgk

WGK 1

flash_point_f

237.2 °F - closed cup

flash_point_c

114 °C - closed cup

ppe

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


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

The developmental toxicity of 2-ethylhexanoic acid in Wistar rats.
Pennanen S, et al.
Fundamental and Applied Toxicology, 19(4), 505-511 (1992)
Synthetic applications of 2-ethylhexanoic acid derived reagents.
Raju R and Prasad K.
Tetrahedron, 68(5), 1341-1349 (2012)
K J French et al.
Biochemistry, 40(32), 9532-9538 (2001-10-05)
This study examines the ability of P450cam to catalyze the formation of 2-ethylhexanoic acid from 2-ethylhexanol relative to its activity on the natural substrate camphor. As is the case for camphor, the P450cam exhibits stereoselectivity for binding (R)- and (S)-2-ethylhexanol.
R Gaudin et al.
International archives of occupational and environmental health, 84(5), 523-531 (2010-08-31)
The aim of this study was to assess, by biological monitoring, workers' exposure to di(2-ethylhexyl) phthalate (DEHP) in the flexible-PVC industry in France to provide additional occupational exposure data, which are particularly scarce. Over 5 days of pre-and post-shift sampling
Shashank Mishra et al.
Chemical Society reviews, 36(11), 1770-1787 (2008-01-25)
This critical review deals with the chemistry and applications of metal alkanoates with medium size (C5 to C12) carbon chain length. A particular emphasis is given to metal 2-ethylhexanoates, which find wide applications as metal-organic precursors in materials science, as

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