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38822-58-1

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38822-58-1 Usage

Description

N-(ε-N-Benzyloxycarbonylamino)caproyl)-β-D-galactopyranosylamine (contains approx 35% Ethanol) is an off-white crystalline solid that is utilized in the preparation of sugar-specific antibodies using liposomes. N-(ε-N-Benzyloxycarbonylamino)caproyl)-β-D-galactopyranosylamine (contains approx 35% Ethanol) is a derivative of galactopyranosylamine, which is a monosaccharide sugar molecule, and is modified with a benzyloxycarbonylamino group and a caproyl group. The presence of approximately 35% ethanol in the compound may serve as a solvent or play a role in the compound's stability or reactivity.

Uses

Used in Pharmaceutical Industry:
N-(ε-N-Benzyloxycarbonylamino)caproyl)-β-D-galactopyranosylamine (contains approx 35% Ethanol) is used as a key component in the preparation of sugar-specific antibodies for various applications in the pharmaceutical industry. N-(ε-N-Benzyloxycarbonylamino)caproyl)-β-D-galactopyranosylamine (contains approx 35% Ethanol)'s ability to form liposomes allows for the targeted delivery of these antibodies to specific cells or tissues, which can be beneficial in the development of therapies for various diseases, including cancer and infectious diseases.
Used in Research and Development:
In the field of research and development, N-(ε-N-Benzyloxycarbonylamino)caproyl)-β-D-galactopyranosylamine (contains approx 35% Ethanol) serves as an important tool for studying the interactions between sugars and proteins, as well as the development of new methods for the synthesis of sugar-specific antibodies. N-(ε-N-Benzyloxycarbonylamino)caproyl)-β-D-galactopyranosylamine (contains approx 35% Ethanol) can be used to investigate the role of sugar molecules in various biological processes and to develop new strategies for the treatment of diseases related to sugar metabolism or sugar-binding proteins.
Used in Diagnostic Applications:
N-(ε-N-Benzyloxycarbonylamino)caproyl)-β-D-galactopyranosylamine (contains approx 35% Ethanol) can also be employed in the development of diagnostic tools and tests that rely on the detection of specific sugar-binding antibodies. By incorporating this compound into the design of diagnostic assays, researchers and clinicians can improve the sensitivity and specificity of these tests, leading to more accurate and reliable diagnoses.

Check Digit Verification of cas no

The CAS Registry Mumber 38822-58-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,2 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 38822-58:
(7*3)+(6*8)+(5*8)+(4*2)+(3*2)+(2*5)+(1*8)=141
141 % 10 = 1
So 38822-58-1 is a valid CAS Registry Number.

38822-58-1SDS

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 benzyl N-[6-oxo-6-[[(2R,4S,5R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]amino]hexyl]carbamate

1.2 Other means of identification

Product number -
Other names N-N-Benzyloxycarbonyl-|A-aminocaproyl-|A-D-galactopyranosylamine

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:38822-58-1 SDS

38822-58-1Downstream Products

38822-58-1Relevant articles and documents

PURIFICATION AND PROPERTIES OF A β-D-MANNOSIDE MANNOHYDROLASE FROM GUAR

McClearly, Barry V.

, p. 75 - 92 (2007/10/02)

A β-D-mannoside mannohydrolase enzyme has been purified to homogeneity from germinated guar-seeds.Difficulties associated with the extraction and purification appeared to be due to an interaction of the enzyme with other protein material.The purified enzyme hydrolysed various natural and synthetic substrates, including β-D-manno-oligosaccharides and reduced β-D-manno-oligosaccharides of degree of polymerisation 2 to 6, as well as p-nitrophenyl, naphthyl, and methylumbelliferyl β-D-mannopyranosides.The preferred, natural substrate was β-D-mannopentaose, which was hydrolysed at twice the rate of β-D-mannotetraose and five times the rate of β-D-mannotriose.This result, together with the observation that α-D-mannose is released on hydrolysis, indicates that the enzyme is an exo-β-D-mannanase.

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