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Methyl palmitate

analytical standard

Synonyme(s) :

Ester méthylique d’acide palmitique

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About This Item

Formule linéaire :
CH3(CH2)14CO2CH3
Numéro CAS:
Poids moléculaire :
270.45
Numéro Beilstein :
1780973
Numéro CE :
Numéro MDL:
Code UNSPSC :
85151701
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Pureté

≥98.5% (GC)

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Indice de réfraction

n20/D 1.4512 (lit.)

Point d'ébullition

185 °C/10 mmHg (lit.)

Pf

32-35 °C (lit.)

Densité

0.852 g/mL at 25 °C (lit.)

Application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Format

neat

Groupe fonctionnel

ester

Conditions d'expédition

ambient

Température de stockage

room temp

Chaîne SMILES 

CCCCCCCCCCCCCCCC(=O)OC

InChI

1S/C17H34O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17(18)19-2/h3-16H2,1-2H3

Clé InChI

FLIACVVOZYBSBS-UHFFFAOYSA-N

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Description générale

Methyl palmitate (MeP) is a high melting point component of biodiesel. It is used in a variety of flavors and fragrances and found abundantly in palm oil-related feedstocks.
Methyl palmitate is a fatty acid methyl ester, which shows potential anti-inflammatory and antifibrotic effects by preventing bleomycin-induced lung inflammation and inhibiting the nuclear factor kappa-β pathway(NF-κB).

Application

Methyl palmitate may be used as an analytical reference standard for the quantification of the analyte in biodiesel samples using chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Produits recommandés

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.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

235.4 °F - closed cup

Point d'éclair (°C)

113.0 °C - closed cup

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)


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Certificats d'analyse (COA)

Lot/Batch Number

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Consulter la Bibliothèque de documents

Anti-inflammatory and antifibrotic effects of methyl palmitate
El-Demerdash E, et al.
Toxicology and Applied Pharmacology, 254(3), 238-244 (2011)
Basic properties of methyl palmitate-diesel blends
Altaie HAM, et al.
Fuel: The Science and Technology of Fuel and Energy, 193(3), 1-6 (2017)
Solvent free synthesis of methyl palmitate over sulfated zirconia solid acid catalyst
Saravanan K, et al.
Fuel: The Science and Technology of Fuel and Energy, 165(3), 298-305 (2016)
Eman M Mantawy et al.
Toxicology and applied pharmacology, 258(1), 134-144 (2011-11-15)
Fibrosis accompanies most chronic liver disorders and is a major factor contributing to hepatic failure. Therefore, the need for an effective treatment is evident. The present study was designed to assess the potential antifibrotic effect of MP and whether MP
Y N Wang et al.
Journal of economic entomology, 102(1), 196-202 (2009-03-04)
Walnut, Juglans regia L., is known for its insecticidal activities to a range of herbivores and microbes. Isolation and identification of bioactive compounds from walnut is a potential approach for the development of new pesticides. Laboratory experiments were carried out

Protocoles

Separation of Methyl erucate; Methyl palmitate; Methyl stearate; Methyl linolenate; Methyl eicosenoate; Methyl behenate; Methyl myristate; Methyl oleate; Methyl arachidate

Separation of Methyl decanoate; Methyl dodecanoate; Methyl myristate; Methyl palmitate; Methyl caprylate; Methyl oleate; Methyl linoleate; Methyl linolenate; Methyl stearate

-11-eicosenoate; Methyl elaidate; Methyl linoleate; Methyl myristate; Methyl myristoleate; Methyl palmitate; Methyl palmitoleate; Methyl oleate; Methyl pentadecanoate; Methyl tridecanoate; Methyl behenate; Methyl caprylate; Methyl erucate; Methyl heptadecanoate; Methyl arachidate

GC Analysis of a 37-Component FAME Mix on Omegawax® (15 m x 0.10 mm I.D., 0.10 μm), Fast GC Analysis

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