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Upenazime is a proteolytic enzyme belonging to the class of proteases, which are enzymes that break down proteins into smaller peptides and amino acids. It is characterized by its high specificity and stability, making it a valuable industrial enzyme for various applications.
Used in Food and Beverage Industry:
Upenazime is used as a processing aid for enhancing cheese and dairy production, brewing, and meat tenderization due to its efficient protein hydrolysis capabilities.
Used in Pharmaceutical Industry:
Upenazime is used as a protein-degrading agent for various pharmaceutical applications, leveraging its ability to break down proteins into smaller components.
Used in Detergent Industry:
Upenazime is used as a protein-degrading enzyme in detergent formulations to enhance the cleaning process by breaking down protein-based stains.

95268-62-5

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95268-62-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95268-62-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,2,6 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 95268-62:
(7*9)+(6*5)+(5*2)+(4*6)+(3*8)+(2*6)+(1*2)=165
165 % 10 = 5
So 95268-62-5 is a valid CAS Registry Number.

95268-62-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (NE)-N-[3-[4-[[(3E)-3-hydroxyimino-2-methylbutan-2-yl]amino]butylamino]-3-methylbutan-2-ylidene]hydroxylamine

1.2 Other means of identification

Product number -
Other names UNII-8663VOR243

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:95268-62-5 SDS

95268-62-5Downstream Products

95268-62-5Relevant academic research and scientific papers

A potentiometric and spectroscopic study of copper(II) diaminodioxime complexes

Jackson, Graham E.,Nakani, Bandile S.

, p. 1373 - 1377 (1996)

Copper(II) and H+ complexes of 3,3,8,8-tetramethyl-4,7-diazadecane-2,9-dione dioxime, 3,3,9,9-tetramethyl-4,8-diazaundecane-2,10-dione dioxime and 3,3,10,10-tetramethyl-4,9-diazadodecane-2,11-dione dioxime have been studied at 25°C and ionic strength 0.15 mol dm-3 NaCl, using glass-electrode potentiometry. Electronic spectra have been used to postulate structures for the different species in solution. In each case the metal binds to the four nitrogen atoms of the oxime. In the MLH-1 species hydrogen bonding between the terminal oxime groups produces a pseudo-macrocycle. Computer simulation has been used to predict the effect of the ligands on the blood-plasma metal-ion distribution in vivo.

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