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M6281

Sigma-Aldrich

Isostearic acid

≥97% (capillary GC)

Synonym(s):

16-Methylheptadecanoic acid

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About This Item

Empirical Formula (Hill Notation):
C18H36O2
CAS Number:
2724-58-5
Molecular Weight:
284.48
EC Number:
220-336-3
MDL number:
MFCD00044082
UNSPSC Code:
12352211
PubChem Substance ID:
24897089
NACRES:
NA.25

Quality Level

100

assay

≥97% (capillary GC)

form

powder

functional group

carboxylic acid

lipid type

saturated FAs

shipped in

ambient

storage temp.

2-8°C

SMILES string

CC(C)CCCCCCCCCCCCCCC(O)=O

InChI

1S/C18H36O2/c1-17(2)15-13-11-9-7-5-3-4-6-8-10-12-14-16-18(19)20/h17H,3-16H2,1-2H3,(H,19,20)

InChI key

XDOFQFKRPWOURC-UHFFFAOYSA-N

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Application

Isostearic acid (16-Methylheptadecanoic acid) is used in the synthesis of methyl-branched poly(hydroxyalkanoate)s, biosurfactants and silver nanoparticles.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Tomonori Oka et al.
Journal of immunology (Baltimore, Md. : 1950), 198(10), 3897-3908 (2017-04-09)
CXCL17 is expressed in a variety of cancers and promotes tumor progression by recruiting myeloid-derived suppressor cells (MDSCs). MDSCs suppress tumor immunity by attracting regulatory T cells (Tregs) into tumor sites through CCL5. In this study, we examined the role
Hsien-Te Hsieh et al.
Langmuir : the ACS journal of surfaces and colloids, 26(12), 10031-10035 (2010-03-20)
This approach provides a new technique to synthesize silver nanoparticles (AgNPs) using CO(2)-expanded liquids (CXLs) as the processing medium. A soluble form of silver carboxylate, silver isostearate (AgISt), was synthesized and characterized. The XRD and DSC analyses indicated that the
Madhu Anand et al.
The journal of physical chemistry. B, 110(30), 14693-14701 (2006-07-28)
The adjustable solvent properties, vanishingly low surface tensions, and environmentally green characteristics of supercritical carbon dioxide present certain advantages in nanoparticles synthesis and processing. Unfortunately, most current techniques employed to synthesize and disperse nanoparticles in carbon dioxide use environmentally persistent
Richard D Ashby et al.
Applied microbiology and biotechnology, 85(2), 359-370 (2009-08-01)
Pseudomonas resinovorans, a known medium-chain-length (mcl-) poly(hydroxyalkanoate) (PHA) producer, was grown on 13-methyltetradecanoic acid (13-MTDA) and a mixture of isostearic acid (IA) isomers to produce methyl-branched mcl-PHA polymers. Shake-flask experiments revealed polymer productivities (the percent of the cell mass that
Veena T Kelleppan et al.
Langmuir : the ACS journal of surfaces and colloids, 34(3), 970-977 (2017-10-11)
Long-chain amidopropyl betaines are known for their ability to self-assemble into viscoelastic wormlike micellar structures. Here, we explore the effect of tailgroup molecular architecture on this process, comparing five molecules, each with C18 chains but different levels of unsaturation and
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