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1956-09-8

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  • Decanoic acid,4-nitrophenyl ester CAS NO.1956-09-8 CAS NO.1956-09-8

    Cas No: 1956-09-8

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1956-09-8 Usage

Description

DECANOIC ACID 4-NITROPHENYL ESTER, also known as 4-Nitrophenyl decanoate, is a chemical compound commonly used in various biochemical and pharmaceutical applications. It is characterized by its ability to act as a substrate for specific enzymes, making it a valuable tool in the assessment of enzyme activity and function.

Uses

Used in Enzyme Activity Assays:
DECANOIC ACID 4-NITROPHENYL ESTER is used as a substrate for assessing the carboxylesterase production by recombinant Penicillium griseoroseum T55 strain. It serves as a reliable indicator of enzyme activity, allowing researchers to evaluate the efficiency and effectiveness of the enzyme in question.
Used in General Esterase Activity Assay:
In the field of biochemistry, DECANOIC ACID 4-NITROPHENYL ESTER is used as a substrate for the general esterase activity assay of hepatopancreas extract. This application aids in understanding the overall esterase activity within the extract, which can be crucial for various research and diagnostic purposes.

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.

Check Digit Verification of cas no

The CAS Registry Mumber 1956-09-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,5 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1956-09:
(6*1)+(5*9)+(4*5)+(3*6)+(2*0)+(1*9)=98
98 % 10 = 8
So 1956-09-8 is a valid CAS Registry Number.

1956-09-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Nitrophenyl decanoate

1.2 Other means of identification

Product number -
Other names (4-nitrophenyl) decanoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1956-09-8 SDS

1956-09-8Relevant articles and documents

-

Blyth,Knowles

, p. 3017,3018 (1971)

-

HIGHER N-ACYL-L-AMINO ACID DERIVATIVES

Kochetkov, K. A.,Urmambetova, Zh. S.,Belikov, V. M.,Bakasova, Z. B.

, p. 2311 - 2316 (2007/10/02)

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.

Murakami,Nakano,Matsumoto

, p. 2996 - 3004 (2007/10/05)

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.

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