1956-09-8

Basic information

• Product Name: DECANOIC ACID 4-NITROPHENYL ESTER
• Synonyms: DECANOIC ACID 4-NITROPHENYL ESTER;4-NITROPHENYL CAPRATE;4-NITROPHENYL DECANOATE;P-NITROPHENYL CAPRATE;4-Nitrophenyl caprate, Decanoic acid 4-nitrophenyl ester;N-[2-[4-[ethyl-[3-(isopropylamino)-2-pyridyl]amino]piperidine-1-carbonyl]-1H-indol-5-yl]methanesulfonamide;N-[2-[4-[ethyl-[3-(propan-2-ylamino)pyridin-2-yl]amino]piperidin-1-yl]carbonyl-1H-indol-5-yl]methanesulfonamide;N-[2-[4-[ethyl-[3-(propan-2-ylamino)pyridin-2-yl]amino]piperidine-1-carbonyl]-1H-indol-5-yl]methanesulfonamide
• CAS NO: 1956-09-8
• Molecular Formula: C₁₆H₂₃NO₄
• Molecular Weight: 293.36
• Mol File: 1956-09-8.mol
• Article Data: 4

Chemical Properties

• Melting Point: ~35 °C
• Appearance: /
• Storage Temp.: 2-8°C
• BRN: 1915230
• CAS DataBase Reference: DECANOIC ACID 4-NITROPHENYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: DECANOIC ACID 4-NITROPHENYL ESTER(1956-09-8)
• EPA Substance Registry System: DECANOIC ACID 4-NITROPHENYL ESTER(1956-09-8)

Safety Data

• Hazard Codes: Xi
• Statements: 43
• Safety Statements: 36/37
• WGK Germany: 3
• F: 8-10-21
• Hazardous Substances Data: 1956-09-8(Hazardous Substances Data)

Usage

Uses

4-Nitrophenyl decanoate has been used as a substrate to assess the carboxylesterase production by recombinant Penicillium griseoroseum T55 strain. It has also been used for general esterase activity assay of the hepatopancreas extract.

Biochem/physiol Actions

4-Nitrophenyl decanoate is a substrate for lipase enzyme. The extracellular lipase has greater hydrolysis reaction velocity with 4-nitrophenyl decanoate when compared with other 4-nitropheny esters.

Upstream product

• 14617-86-8 4-nitrophenyl stearate 
• 100-02-7 4-nitro-phenol 
• 334-48-5 1-decanoic acid 
• 112-13-0 n-decanoyl chloride 

Downstream Products

• 4195-18-0 4-nitrophenyl 4-methylpentanoate 
• 2635-84-9 p-nitrophenyl butyrate 
• 956-75-2 p-nitrophenyl hexanoate 
• 13551-17-2 cyclohexanecarboxylic acid 4-nitrophenyl ester 
• 17895-71-5 p-nitrophenyl hydrocinnamate 
• 959-22-8 p-nitrophenylbenzoate 
• 42721-91-5 4-nitrophenyl cyclopentanecarboxylate 
• 26050-99-7 p-nitrophenyl cyclopropanecarboxylate 
• 72289-61-3 phenyl-2 butyrate de p-nitrophenyle 
• 830-03-5 4-nitrophenol acetate 
• 321865-45-6 cyclobutanecarboxylic acid 4-nitrophenyl ester 
• 104013-15-2 2-phenylpropionic acid p-nitrophenyl ester 
• 110-42-9 Methyl decanoate 
• 60160-17-0 2-heptyl decanoate 

Relevant articles and documents

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HIGHER N-ACYL-L-AMINO ACID DERIVATIVES

A preparative method is proposed for obtaining higher N-acylamino acids by reaction of free amino acids with fatty acid nitrophenyl esters.It was shown that these acids can transport positive ions through a liquid lipophilic medium.A direct method is proposed for obtaining fatty acid 4-nitrophenyl esters by boiling 4-nitrophenol and the fatty acid in xylene in a Soxhlet apparatus in the presence of an acid catalyst.

CATALYTIC EFFICIENCY OF SYNTHETIC MICELLAR CATALYSTS BEARING A MERCAPTO GROUP AS THE REACTION CENTER.

In order to obtain a clue to understanding the micro-environmental effect on the reactivity of a mercapto group placed in a reaction center of enzymes, micellar surfactants bearing a mercapto group were synthesized and their catalytic activity in the degradation of p-nitrophenyl carboxylates was studied. N-Hexadecyl-N** alpha -glutaryl-L-cysteinamide (AM multiplied by (times) Cys-1) has an ability to form anionic micelles in aqueous media. The catalytic activity of AM multiplied by (times) Cys-1 was compared with that of another synthetic surfactant, N-hexadecanoyl-L-cysteine (AM multiplied by (times) Cys-2). These surfactants below their critical micelle concentations markedly accelerated the degradation of several p-nitrophenyl carboxylates. On the contrary, the concentration-rate profiles for the degradation of p-nitrophenyl dodecanoate (PNPL) as catalyzed by the surfactants indicate that the reactivity of the mercapto group is reduced upon formation of the anionic micelles.