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Supelco

Stearyl stearate

analytical standard

Sinonimo/i:

Stearic acid stearyl ester

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About This Item

Formula condensata:
CH3(CH2)16COO(CH2)17CH3
Numero CAS:
Peso molecolare:
536.96
Beilstein:
1807499
Numero CE:
Numero MDL:
Codice UNSPSC:
85151701
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Saggio

≥98% (GC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Formato

neat

Gruppo funzionale

ester

Temperatura di conservazione

room temp

Stringa SMILE

CCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCC

InChI

1S/C36H72O2/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-38-36(37)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-35H2,1-2H3
NKBWPOSQERPBFI-UHFFFAOYSA-N

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Descrizione generale

Stearyl stearate is the ester of stearic acid and 1-octadecanol.

Applicazioni

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Stearyl stearate may be used as a model lipid to stain contact lenses in evaluating the lipid-degrading ability of the cholesterol esterase enzyme produced from Pseudomonas aeruginosa.

Prodotti consigliati

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Codice della classe di stoccaggio

11 - 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

Eyeshields, Gloves, type N95 (US)


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Certificati d'analisi (COA)

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Purification and characterization of a novel cholesterol esterase from Pseudomonas aeruginosa, with its application to cleaning lipid-stained contact lenses.
Sugihara A.
Bioscience, Biotechnology, and Biochemistry, 66(11), 2347-2355 (2002)
Derivatisation using m-(trifluoromethyl) phenyltrimethylammonium hydroxide of organic materials in artworks for analysis by gas chromatography?mass spectrometry: unusual reaction products with alcohols.
Sutherland K.
Journal of Chromatography A, 1149(1), 30-37 (2007)
Dorothy M Duffy et al.
Langmuir : the ACS journal of surfaces and colloids, 20(18), 7630-7636 (2004-08-25)
Living organisms can control the size, shape, and structure of minerals. Attempts to reproduce this biological control in the laboratory often use Langmuir monolayers of long-chain carboxylic acids. We use large-scale molecular dynamics simulations to calculate the interfacial energies of
K Maeda et al.
Journal of chromatography, 221(2), 199-204 (1980-12-12)
A gas chromatographic--mass spectrometric analysis was used to separate and identify abnormal compounds in the nail of psoriatic patients. The nail was extracted with heated ethanol, and the extract was analyzed with and without trimethylsilylation. Tetradecanoic acid octadecyl ester, hexadecanoic

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