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H9631

Sigma-Aldrich

DL-α-Hydroxystearic acid

≥99%

Sinónimos:

D,L-2-hydroxystearic acid, 2-Hydroxyoctadecanoic acid

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About This Item

Fórmula empírica (notación de Hill):
C18H36O3
Número de CAS:
629-22-1
Peso molecular:
300.48
MDL number:
MFCD00046526
UNSPSC Code:
12352211
PubChem Substance ID:
24895861
NACRES:
NA.25

biological source

synthetic (organic)

Quality Level

200

assay

≥99%

form

powder

functional group

carboxylic acid

lipid type

saturated FAs

shipped in

ambient

storage temp.

2-8°C

SMILES string

CCCCCCCCCCCCCCCCC(O)C(O)=O

InChI

1S/C18H36O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17(19)18(20)21/h17,19H,2-16H2,1H3,(H,20,21)

InChI key

KIHBGTRZFAVZRV-UHFFFAOYSA-N

Categorías relacionadas

Biochem/physiol Actions

DL-α-Hydroxystearic acid is a mixture of D and L-α-hydroxystearic acid (2-Hydroxyoctadecanoic acid) enantiomers. α-Hydroxystearic may be used in studies on the properties and metabolism of α-hydroxylated (2-hydroxylated) medium chain fatty acids.

Packaging

Sealed ampule.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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M Salim-Hanna et al.
Lipids, 24(8), 750-752 (1989-08-01)
Combined--but not individual--microsomal and supernatant fractions obtained from rat brains not only consume oxygen but also provoke emission from added chlorophyll. These results are consistent with literature data (Levis and Mead, J. Biol. Chem. 239, 77 [1964]) for trapping of
Samanta R Zanetti et al.
Biochimie, 92(12), 1778-1786 (2010-09-14)
Sphingolipids from rodent testis and spermatozoa are known to contain non-hydroxylated (N-) and 2-hydroxylated (2-OH) very-long-chain polyunsaturated fatty acids (VLCPUFA). In this study, the contribution of species with each type of fatty acids to the total ceramides (Cer) and sphingomyelins
Conrad D Lendrum et al.
Langmuir : the ACS journal of surfaces and colloids, 27(8), 4430-4438 (2011-03-23)
2-Hydroxyacids display complex monolayer phase behavior due to the additional hydrogen bonding afforded by the presence of the second hydroxy group. The placement of this group at the position α to the carboxylic acid functionality also introduces the possibility of
R Schütz et al.
International journal of cosmetic science, 41(3), 240-256 (2019-04-08)
We report on the preparation and efficacy of 10-hydroxystearic acid (HSA) that improves facial age spots and conspicuous pores. The hydration of oleic acid into HSA was catalyzed by the oleate hydratase from Escherichia coli. Following treatment with HSA, collagen
Voradanu Visetvichaporn et al.
International journal of pharmaceutics, 573, 118772-118772 (2019-11-26)
HL235 is a new cathepsin K inhibitor designed and synthesized to treat osteoporosis. Since HL235 has poor aqueous solubility, a self-microemulsifying drug delivery system (SMEDDS) was formulated to enhance its oral bioavailability. A solubility study of HL235 was performed to
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