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95268-62-5

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95268-62-5 Usage

General Description

Upenazime is a chemical compound commonly used as an industrial enzyme for various applications. It belongs to the class of enzymes called proteases, which are responsible for breaking down proteins into smaller peptides and amino acids. Upenazime is specifically used for its ability to efficiently hydrolyze proteins and is widely utilized in the food and beverage industry for processes such as cheese and dairy production, brewing, and meat tenderization. It is also used in the pharmaceutical and detergent industries for its protein-degrading properties. Upenazime is known for its high specificity and stability, making it a valuable tool for many commercial applications.

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 articles and documents

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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