Skip to Content
Merck
CN

75940

2-Oxooctanoic acid

≥99.0% (T)

Synonym(s):

α-Ketooctanoic acid, 2-Oxocaprylic acid

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
CH3(CH2)5COCOOH
CAS Number:
Molecular Weight:
158.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-331-9
Beilstein/REAXYS Number:
1757862
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

2-Oxooctanoic acid, ≥99.0% (T)

InChI key

GPPUPQFYDYLTIY-UHFFFAOYSA-N

InChI

1S/C8H14O3/c1-2-3-4-5-6-7(9)8(10)11/h2-6H2,1H3,(H,10,11)

SMILES string

CCCCCCC(=O)C(O)=O

assay

≥99.0% (T)

form

flakes

bp

82 °C/0.05 mmHg

mp

33-36 °C

functional group

carboxylic acid
ketone

storage temp.

2-8°C

Quality Level

Looking for similar products? Visit Product Comparison Guide

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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

Huifang Xu et al.
Journal of colloid and interface science, 509, 265-274 (2017-09-16)
Single-tailed short-chain alkyl keto-acids/salts, a class of fatty acid/salt derivatives, such as sodium 2-ketooctanate (KOCOONa), are a kind of weakly acid/salt type amphiphiles and plausible prebiotic molecules, and the current understanding of their aggregation behavior in aqueous solutions is still
Sarah A Almahboub et al.
Applied microbiology and biotechnology, 102(2), 789-799 (2017-11-28)
Terminal modification of peptides is frequently used to improve their hydrophobicity. While N-terminal modification with fatty acids (lipidation) has been reported previously, C-terminal lipidation is limited as it requires the use of linkers. Here we report the use of a

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