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Merck
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73297

Sigma-Aldrich

Miscela acido palmitico-acido stearico

tested according to Ph. Eur.

Sinonimo/i:

Acidi grassi C16-18, Miscela acido stearico-acido palmitico

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About This Item

Numero CAS:
67701-03-5
Beilstein:
608585
Numero CE:
266-928-5
Numero MDL:
MFCD00002752
Codice UNSPSC:
12352106
ID PubChem:
329764775
NACRES:
NA.25

Origine biologica

palm oil

Livello qualitativo

100

agenzia

USP/NF
tested according to Ph. Eur.

Saggio

≥90% (sum of steric acid and palmitic acid)

Forma fisica

liquid

Gruppo funzionale

carboxylic acid

Condizioni di spedizione

ambient

Temperatura di conservazione

room temp

Stringa SMILE

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)
QIQXTHQIDYTFRH-UHFFFAOYSA-N

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Altre note

mixture of fatty acids, consisting mainly of stearic acid and 40-60% palmitic acid (acc. to Ph.Eur.)

Codice della classe di stoccaggio

13 - Non Combustible Solids

Classe di pericolosità dell'acqua (WGK)

nwg

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
BCCL5542
BCCK1574
BCCJ3501
BCCH7279
BCCH5350

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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).
Arpita Chatterjee et al.
Antimicrobial agents and chemotherapy, 52(1), 220-224 (2007-10-24)
Cholera toxin (CT) is an archetypal bacterial toxin that binds with a high affinity to the receptor ganglioside GM1 on the intestinal epithelial surface and that causes the severe watery diarrhea characteristic of the disease cholera. Blockage of the interaction
Marcy J Balunas et al.
Journal of natural products, 69(4), 700-703 (2006-04-29)
Natural product drug discovery efforts frequently utilize noncellular screening assays. Fatty acids are commonly found in natural product extracts, and some have been shown to interfere with noncellular assays. Several pure fatty acids were tested using a noncellular aromatase assay
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