73297
Solution d′acide palmitique / acide stéarique
tested according to Ph. Eur.
Synonyme(s) :
Acides gras en C16-18, Mélange d’acide stéarique / acide palmitique
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A propos de cet article
Numéro CAS:
UNSPSC Code:
12352106
NACRES:
NA.25
PubChem Substance ID:
EC Number:
266-928-5
Beilstein/REAXYS Number:
608585
MDL number:
Service technique
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Laissez-nous vous aiderbiological source
palm oil
Quality Level
agency
tested according to Ph. Eur.
assay
≥90% (sum of steric acid and palmitic acid)
form
liquid
functional group
carboxylic acid
shipped in
ambient
storage temp.
room temp
SMILES string
CCCCCCCCCCCCCCCCCC(O)=O
InChI
1S/C18H36O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h2-17H2,1H3,(H,19,20)
InChI key
QIQXTHQIDYTFRH-UHFFFAOYSA-N
Other Notes
mixture of fatty acids, consisting mainly of stearic acid and 40-60% palmitic acid (acc. to Ph.Eur.)
Classe de stockage
13 - Non Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Palle J Pedersen et al.
Journal of medicinal chemistry, 53(9), 3782-3792 (2010-04-22)
The design of retinoid phospholipid prodrugs is described based on molecular dynamics simulations and cytotoxicity studies of synthetic retinoid esters. The prodrugs are degradable by secretory phospholipase A(2) IIA and have potential in liposomal drug delivery targeting tumors. We have
Jih-Jung Chen et al.
Journal of natural products, 72(2), 223-228 (2009-02-06)
Six new compounds, including five new seco-abietane diterpenoids, 12-deoxy-seco-hinokiol methyl ester (1), 12-deoxy-11,12-dihydro-seco-hinokiol methyl ester (2), callicarpic acid A (3), 9alpha-hydroxycallicarpic acid A (4), and callicarpic acid B (5), and a new phenylethanoid derivative, 4-hydroxyphenethyl tetradecanoate (6), have been isolated
Bhadreshkumar B Maisuria et al.
Bioorganic & medicinal chemistry, 19(9), 2918-2926 (2011-04-16)
Homologous dicarboxyl dendritic amphiphiles-RCONHC(CH(3))(CH(2)CH(2)COOH)(2), 4(n); and ROCONHC(CH(3))(CH(2)CH(2)COOH)(2), 5(n), where R=n-C(n)H(2)(n)(+1) and n=13-22 carbon atoms-were synthesized. Critical micelle concentrations (CMCs) in aqueous triethanolamine solutions and at pH 7.4 were measured along with hemolytic activity (effective concentrations, EC(10)) in phosphate-buffered saline (PBS).