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:
Molecular Weight:
256.42
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
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
SMILES string
CCCCCCCCC(CCCCCC)C(O)=O
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)
InChI key
JMOLZNNXZPAGBH-UHFFFAOYSA-N
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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 2 - Skin Irrit. 2 - Skin Sens. 1B
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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)
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
Ester synthesis by the lipase from Pseudomonas fragi 22.39 B.
Nishio T, et al.
Agricultural and Biological Chemistry, 52(5), 1203-1208 (1988)
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
Shixiong Gao et al.
Environmental science & technology, 53(5), 2862-2872 (2019-02-12)
Exposure to environmental chemicals could disturb lipidome homeostasis in biotas. Comprehensive identification and interpretation of lipid molecules in biological samples are of great importance to elucidate the potential changes in lipid homeostasis upon exposure to various environmental stimuli. In this
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