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464449

Sigma-Aldrich

2-Hexyldecanoic acid

96%

Sinônimo(s):

2-n-Hexyldecanoic acid, Isopalmitic acid

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About This Item

Fórmula linear:
CH3(CH2)7CH[(CH2)5CH3]CO2H
Número CAS:
25354-97-6
Peso molecular:
256.42
Número CE:
246-885-9
Número MDL:
MFCD00059651
Código UNSPSC:
12352100
ID de substância PubChem:
24870182
NACRES:
NA.22

Ensaio

96%

índice de refração

n20/D 1.446 (lit.)

pb

268 °C (lit.)

pf

18 °C (lit.)

densidade

0.874 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

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)

chave InChI

JMOLZNNXZPAGBH-UHFFFAOYSA-N

Descrição geral

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

Aplicação

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.

Pictogramas

Exclamation markEnvironment
GHS07,GHS09

Palavra indicadora

Warning

Frases de perigo

H315,H317,H410

Classificações de perigo

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

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

235.4 °F - closed cup

Ponto de fulgor (°C)

113 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Core-shell-structured highly branched poly (ethylenimine amide) s: synthesis and structure.
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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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