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Merck
CN

464449

2-Hexyldecanoic acid

96%

Synonym(s):

2-n-Hexyldecanoic acid, Isopalmitic acid

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About This Item

Linear Formula:
CH3(CH2)7CH[(CH2)5CH3]CO2H
CAS Number:
25354-97-6
Molecular Weight:
256.42
NACRES:
NA.22
PubChem Substance ID:
24870182
UNSPSC Code:
12352100
EC Number:
246-885-9
MDL number:
MFCD00059651
Assay:
96%

Key Documents

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InChI key

JMOLZNNXZPAGBH-UHFFFAOYSA-N

InChI

1S/C16H32O2/c1-3-5-7-9-10-12-14-15(16(17)18)13-11-8-6-4-2/h15H,3-14H2,1-2H3,(H,17,18)

SMILES string

CCCCCCCCC(CCCCCC)C(O)=O

assay

96%

refractive index

n20/D 1.446 (lit.)

bp

268 °C (lit.)

mp

18 °C (lit.)

density

0.874 g/mL at 25 °C (lit.)

functional group

carboxylic acid

Quality Level

100

Related Categories

General description

2-Hexyldecanoic acid is a carboxylic acid having branched carbon chains.

Application

2-Hexyldecanoic acid may be used as amidating agent for the suppression of side-chain crystallization during the synthesis of amphiphilic macromolecules. It may be employed as a surrogate carboxylic acid in a study.

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 2 - Skin Irrit. 2 - Skin Sens. 1B

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
05308KJ
06206LI
05518LI
09921KQ

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Core-shell-structured highly branched poly (ethylenimine amide) s: synthesis and structure.
Antonietti L, et al.
Macromolecules, 38(14), 5914-5920 (2005)
Ester synthesis by the lipase from Pseudomonas fragi 22.39 B.
Nishio T, et al.
Agricultural and Biological Chemistry, 52(5), 1203-1208 (1988)
Mohamed H Mohamed et al.
Rapid communications in mass spectrometry : RCM, 23(23), 3703-3712 (2009-11-10)
Aqueous solutions containing simple model aliphatic and alicyclic carboxylic acids (surrogates 1-4) were studied using negative ion electrospray mass spectrometry (ESI-MS) in the presence and absence of alpha-, beta-, and gamma-cyclodextrin. Molecular ions were detected corresponding to the parent carboxylic
Liheng Wu et al.
Nature, 548(7666), 197-201 (2017-08-02)
Crystallization of colloidal nanocrystals into superlattices represents a practical bottom-up process with which to create ordered metamaterials with emergent functionalities. With precise control over the size, shape and composition of individual nanocrystals, various single- and multi-component nanocrystal superlattices have been
Beili Wang et al.
Environmental science & technology, 53(2), 1022-1030 (2018-12-18)
The nontargeted scanning chemical profiling approach has shown great potential to identify unknown pollutants or novel biological markers; however, the structure identification of unknown compounds is a challenge. In this study, a carboxyl-specific derivatization reagent, N-(4-aminomethylphenyl) pyridinium (AMPP), was coupled
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