H9631
DL-α-Hydroxystearic acid
≥99%
Sinonimo/i:
D,L-2-hydroxystearic acid, 2-Hydroxyoctadecanoic acid
Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Scegli un formato
25 MG
191,00 €
Scegli un formato
Cambia visualizzazione
25 MG
191,00 €
About This Item
Formula empirica (notazione di Hill):
C18H36O3
Numero CAS:
Peso molecolare:
300.48
Numero MDL:
Codice UNSPSC:
12352211
ID PubChem:
NACRES:
NA.25
Prodotti consigliati
Origine biologica
synthetic (organic)
Saggio
≥99%
Stato
powder
Gruppo funzionale
carboxylic acid
Tipo di lipide
saturated FAs
Condizioni di spedizione
ambient
Temperatura di conservazione
2-8°C
Stringa SMILE
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)
KIHBGTRZFAVZRV-UHFFFAOYSA-N
Categorie correlate
Azioni biochim/fisiol
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.
Confezionamento
Sealed ampule.
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
Scegli una delle versioni più recenti:
Possiedi già questo prodotto?
I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.
I clienti hanno visto anche
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
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
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
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
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
Filtri attivi
Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..
Contatta l'Assistenza Tecnica.
