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56599-69-0

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56599-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56599-69-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,9 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56599-69:
(7*5)+(6*6)+(5*5)+(4*9)+(3*9)+(2*6)+(1*9)=180
180 % 10 = 0
So 56599-69-0 is a valid CAS Registry Number.

56599-69-0Downstream Products

56599-69-0Relevant articles and documents

Eicosapentaenoic acid enrichment from sardine oil by argentation chromatography

Chakraborty, Kajal,Raj, R. Paul

, p. 7586 - 7595 (2008/09/19)

Eicosapentaenoic acid (EPA) derived from chemically hydrolyzed sardine oil was concentrated by urea fractionation using methanol at different temperatures (2, 4, and 6°C) and urea/fatty acid ratios (2:1, 3:1, and 4:1 w/w) and purified by argentation neutral alumina column chromatography. The individual fatty acids were determined as fatty acid methyl esters (FAME) by gas-liquid chromatography and gas chromatography-mass spectroscopy as FAME and N-acyl pyrrolidides. In the mass fragmentation pattern of FAME, the base peak was assigned to be the 1-methoxyethenol moiety (m/z = 74) obtained by McLafferty rearrangement. Formation of the cyclic tropylium ion (m/z = 91) in fatty acids with four or more double bonds was apparent in FAME-PUFAs. The base peak of N-acyl pyrrolidides was the McLafferty rearrangement ion, 1-(pyrrolidin-1-yl) ethenol (m/z = 113). The highest concentration of EPA (47.78%) was obtained at the crystallization temperature of 4°C with a urea/fatty acid ratio of 4:1 (w/w) with 93.74% yield. After complexation of saturated and less unsaturated fatty acids by urea complexation, argentation chromatography resulted in an EPA of high purity (99.6%) with an overall recovery of 54.09% using 50% diethyl ether/n-hexane as eluting solvent. The peroxide (POV) and thiobarbituric acid (TBS) values were found to be highest (4.0 mequiv of O2/kg and 5.2 mg of malondialdehyde/kg, respectively) during urea fractionation at the higher crystallization temperature (6°C) and higher urea/fatty acid ratio (4:1).

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