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54322-38-2

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54322-38-2 Usage

Description

4-METHYLUMBELLIFERYL-ALPHA-L-FUCOPYRANOSIDE, also known as 4-MUF, is a synthetic compound derived from fucopyranosides, which are a type of sugar found in various biological systems. It is a white powder with unique chemical properties that make it useful in various applications, particularly as a biological indicator.

Uses

Used in Sterilization Processes:
4-METHYLUMBELLIFERYL-ALPHA-L-FUCOPYRANOSIDE is used as a biological indicator for sterilization processes in the medical and pharmaceutical industries. It serves as a reliable marker to ensure that sterilization procedures have been effective in eliminating harmful microorganisms, such as bacteria, viruses, and fungi, from medical equipment and pharmaceutical products.
Used in Research and Development:
In the field of research and development, 4-METHYLUMBELLIFERYL-ALPHA-L-FUCOPYRANOSIDE is used as a substrate for the detection and analysis of fucosidase enzymes. These enzymes are involved in the breakdown of fucopyranosides and are essential for various biological processes. By using 4-MUF as a substrate, researchers can study the activity and function of fucosidase enzymes, which can contribute to the understanding of various diseases and the development of potential therapeutic strategies.
Used in Quality Control:
4-METHYLUMBELLIFERYL-ALPHA-L-FUCOPYRANOSIDE is also utilized in the quality control of pharmaceutical products, particularly those containing fucopyranosides. By measuring the activity of fucosidase enzymes in the presence of 4-MUF, quality control teams can ensure that the products meet the required standards and are safe for use.

Check Digit Verification of cas no

The CAS Registry Mumber 54322-38-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,3,2 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54322-38:
(7*5)+(6*4)+(5*3)+(4*2)+(3*2)+(2*3)+(1*8)=102
102 % 10 = 2
So 54322-38-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H18O7/c1-7-5-12(17)23-11-6-9(3-4-10(7)11)22-16-15(20)14(19)13(18)8(2)21-16/h3-6,8,13-16,18-20H,1-2H3/t8-,13+,14+,15-,16-/m0/s1

54322-38-2SDS

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-METHYLUMBELLIFERYL-α-L-FUCOPYRANOSIDE

1.2 Other means of identification

Product number -
Other names -

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:54322-38-2 SDS

54322-38-2Downstream Products

54322-38-2Relevant articles and documents

CARBONIC ANHYDRASE INHIBITORS WITH ANTIMETASTATIC ACTIVITY

-

Page/Page column 22-29, (2012/06/15)

Compositions for the treatment of cancer comprising coumarin and thiocoumarin derivatives of Formulas I- XII are disclosed. Said derivatives preferentially inhibit carbonic anhydrase IX and XII (which are associated with hypoxic and metastatic tumours) over inhibiting carbonic anhydrase I and II activity. The compositions therefore are suited for treatment of hypoxic or metastatic cancers due to this selective mechanism of action.

Profiling of glycosidase activities using coumarin-conjugated glycoside cocktails

Park, Sungjin,Shin, Injae

, p. 619 - 622 (2007/10/03)

Glycosidases are a large subgroup of carbohydrate-processing enzymes that hydrolytically cleave the glycosidic bond. Glycans formed by the action of glycosidases are involved in various biological processes. Genetic abnormalities in glycosidases are associated with inherited diseases. Thus, characterization of the catalytic activities of glycosidases is of great importance. Herein, we describe a simple and rapid approach for determining glycosidase activity profiles using coumarin-conjugated glycoside cocktails.

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