CRM1891
F.A.M.E. Mix GLC-10
certified reference material, pkg of 100 mg (Neat)
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About This Item
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grade
certified reference material
TraceCERT®
Quality Level
product line
TraceCERT®
form
liquid
CofA
certificate is enclosed in each package
packaging
pkg of 100 mg (Neat)
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
application(s)
food and beverages
format
multi-component solution
functional group
carboxylic acid
ester
shipped in
dry ice
storage temp.
-10 to -25°C
General description
This certified reference material is useful for determining relative retention times and approximating response factors.
Check out our complete portfolio of Fatty acid methyl ester (FAME) reference material solution mixes
Check out our complete portfolio of Fatty acid methyl ester (FAME) reference material solution mixes
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Other Notes
This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.
Legal Information
TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany
Analyte
Description
Methyl linoleate 20 wt. %
Methyl linolenate 20 wt. %
Methyl oleate 20 wt. %
Methyl palmitate 20 wt. %
Methyl stearate 20 wt. %
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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The Analyst, 144(19), 5848-5855 (2019-09-05)
The carbon-carbon double bond positions of unsaturated fatty acids can have markedly different effects on biological function and also serve as biomarkers of disease pathology, dietary history, and species identity. As such, there is great interest in developing methods for
Reproduction (Cambridge, England), 153(2), 175-185 (2016-12-07)
Hormone-sensitive lipase-knockout (HSL-/-) mice exhibit azoospermia for unclear reasons. To explore the basis of sterility, we performed the following three experiments. First, HSL protein distribution in the testis was determined. Next, transcriptome analyses were performed on the testes of three
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