H9631
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:
Peso molecular:
300.48
Número MDL:
Código UNSPSC:
12352211
ID de la sustancia en PubChem:
NACRES:
NA.25
Productos recomendados
origen biológico
synthetic (organic)
Nivel de calidad
Ensayo
≥99%
Formulario
powder
grupo funcional
carboxylic acid
tipo de lípido
saturated FAs
Condiciones de envío
ambient
temp. de almacenamiento
2-8°C
cadena SMILES
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)
Clave InChI
KIHBGTRZFAVZRV-UHFFFAOYSA-N
Categorías relacionadas
Acciones bioquímicas o fisiológicas
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.
Envase
Sealed ampule.
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Equipo de protección personal
Eyeshields, Gloves, type N95 (US)
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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
S Sonnino et al.
Chemistry and physics of lipids, 69(2), 95-104 (1994-02-01)
GM1 ganglioside containing a hydroxylated fatty acid moiety, GM1(OH), was synthesized starting from lyso-GM1 and D-(+)-2-hydroxystearic acid. The aggregative, geometrical and distribution properties of GM1(OH) were compared with those of stearic acid containing GM1 ganglioside; laser light scattering measurements, differential
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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
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