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p-Nitrophenyl linoleate (PNPL) is a synthetic ester compound that serves as a substrate for various lipase enzymes, which are responsible for breaking down fats. It is widely used in biochemical research and assays to study the activity and specificity of lipases. PNPL consists of a p-nitrophenol group attached to a linoleic acid chain, which allows for the colorimetric detection of lipase activity through the release of p-nitrophenol upon hydrolysis. p-nitrophenyl linoleate is particularly useful in the study of enzyme kinetics, as the absorbance of the released p-nitrophenol can be easily measured, providing a quantitative assessment of lipase activity.

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  • 6562-50-1 Structure
  • Basic information

    1. Product Name: p-nitrophenyl linoleate
    2. Synonyms: p-nitrophenyl linoleate
    3. CAS NO:6562-50-1
    4. Molecular Formula:
    5. Molecular Weight: 401.546
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 6562-50-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: p-nitrophenyl linoleate(CAS DataBase Reference)
    10. NIST Chemistry Reference: p-nitrophenyl linoleate(6562-50-1)
    11. EPA Substance Registry System: p-nitrophenyl linoleate(6562-50-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 6562-50-1(Hazardous Substances Data)

6562-50-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6562-50-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,6 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6562-50:
(6*6)+(5*5)+(4*6)+(3*2)+(2*5)+(1*0)=101
101 % 10 = 1
So 6562-50-1 is a valid CAS Registry Number.

6562-50-1Downstream Products

6562-50-1Relevant articles and documents

Alteration of Chain Length Selectivity of Candida antarctica Lipase A by Semi-Rational Design for the Enrichment of Erucic and Gondoic Fatty Acids

Zorn, Katja,Oroz-Guinea, Isabel,Brundiek, Henrike,D?rr, Mark,Bornscheuer, Uwe T.

, p. 4115 - 4131 (2018)

Biotechnological strategies using renewable materials as starting substrates are a promising alternative to traditional oleochemical processes for the isolation of different fatty acids. Among them, long chain mono-unsaturated fatty acids are especially interesting in industrial lipid modification, since they are precursors of several economically relevant products, including detergents, plastics and lubricants. Therefore, the aim of this study was to develop an enzymatic method in order to increase the percentage of long chain mono-unsaturated fatty acids from Camelina and Crambe oil ethyl ester derivatives, by using selective lipases. Specifically, the focus was on the enrichment of gondoic (C20:1 cisΔ11) and erucic acid (C22:1 cisΔ13) from Camelina and Crambe oil derivatives, respectively. The pursuit of this goal entailed several steps, including: (i) the choice of a suitable lipase scaffold to serve as a protein engineering template (Candida antarctica lipase A); (ii) the identification of potential amino acid targets to disrupt the binding tunnel at the adequate location; (iii) the design, creation and high-throughput screening of lipase mutant libraries; (iv) the study of the selectivity towards different chain length p-nitrophenyl fatty acid esters of the best hits found, as well as the analysis of the contribution of each amino acid change and the outcome of combining several of the aforementioned residue alterations and, finally, (v) the selection and application of the most promising candidates for the fatty acid enrichment biocatalysis. As a result, enrichment of C22:1 from Crambe ethyl esters was achieved either, in the free fatty acid fraction (wt, 78%) or in the esterified fraction (variants V1, 77%; V9, 78% and V19, 74%). Concerning the enrichment of C20:1 when Camelina oil ethyl esters were used as substrate, the best variant was the single mutant V290W, which doubled its content in the esterified fraction from approximately 15% to 34%. A moderately lower increase was achieved by V9 and its two derived triple mutant variants V19 and V20 (27%). (Figure presented.).

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