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4-Nitrophenyl phosphate bis(cyclohexylammonium) salt is a chemical compound utilized in biochemical research and diagnostic assays. It is a salt form of 4-nitrophenyl phosphate, serving as a substrate for detecting alkaline phosphatase activity. The presence of cyclohexylammonium ions in the compound enhances its solubility in aqueous solutions, making it suitable for various applications in the field of biochemistry.

52483-84-8

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52483-84-8 Usage

Uses

Used in Biochemical Research:
4-Nitrophenyl phosphate bis(cyclohexylammonium) salt is used as a substrate in biochemical research for the detection of alkaline phosphatase activity. Its ability to solubilize in aqueous solutions allows for its use in a wide range of assays and experiments.
Used in Colorimetric Assays:
In colorimetric assays, 4-Nitrophenyl phosphate bis(cyclohexylammonium) salt is used as an indicator to measure alkaline phosphatase activity in biological samples. The release of 4-nitrophenol upon enzymatic hydrolysis results in a color change, allowing for the quantification of enzyme activity.
Used in Enzyme-Linked Immunosorbent Assays (ELISA):
4-Nitrophenyl phosphate bis(cyclohexylammonium) salt is employed as a detection agent in ELISA, where it serves as a substrate for alkaline phosphatase-conjugated antibodies. The enzymatic conversion of the substrate to 4-nitrophenol provides a colorimetric signal that can be measured and correlated with the presence of specific antigens in the sample.
Used in Medical Diagnostic Tests:
4-Nitrophenyl phosphate bis(cyclohexylammonium) salt is utilized in the development of medical diagnostic tests, particularly those that involve the detection and quantification of alkaline phosphatase activity. Its use in these tests aids in the diagnosis and monitoring of various diseases and conditions.
Used in Laboratory Research for Enzyme Kinetics and Protein Function:
In laboratory research, 4-Nitrophenyl phosphate bis(cyclohexylammonium) salt is used to study enzyme kinetics and protein function. Its role as a substrate for alkaline phosphatase allows researchers to investigate the enzyme's activity, mechanism, and interactions with other molecules, contributing to a deeper understanding of biological processes and potential therapeutic targets.

Check Digit Verification of cas no

The CAS Registry Mumber 52483-84-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,8 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 52483-84:
(7*5)+(6*2)+(5*4)+(4*8)+(3*3)+(2*8)+(1*4)=128
128 % 10 = 8
So 52483-84-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H6NO6P.2C6H13N.H2O/c8-7(9)5-1-3-6(4-2-5)13-14(10,11)12;2*7-6-4-2-1-3-5-6;/h1-4H,(H2,10,11,12);2*6H,1-5,7H2;1H2

52483-84-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Nitrophenyl phosphate bis(cyclohexylammonium) salt

1.2 Other means of identification

Product number -
Other names cyclohexanamine,(4-nitrophenyl) dihydrogen phosphate

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:52483-84-8 SDS

52483-84-8Downstream Products

52483-84-8Relevant academic research and scientific papers

Bis phosphochloridate, a new phosphorylating agent

Beld, A.,Claesen, C. A. A.,Roersma, E. S.,Schippers, W. J. M.,Keizer, L. M.,Tesser, G. I.

, p. 196 - 202 (2007/10/02)

This communication describes the application of the 2-(methylsulfonyl)ethyl group (Mse) as a base-labile protecting group for the two hydroxyl functions in phosphoric acid monoesters.Due to its perfect stability towards acids, the Mse group can function a

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