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3687-64-7

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3687-64-7 Usage

Description

Galactinol Dihydrate is an α-galactoside of inositol, which serves as the structural basis for various signaling and secondary messenger molecules. It plays a crucial role in processes such as insulin signal transduction, cytoskeleton assembly, nerve guidance, membrane potentials, serotonin activity, and the breakdown of fats and cholesterol reduction.

Uses

Used in Pharmaceutical Industry:
Galactinol Dihydrate is used as a key component in the development of drugs targeting various physiological processes. Its involvement in insulin signal transduction, cytoskeleton assembly, and nerve guidance makes it a valuable asset for creating medications that address a wide range of health issues.
Used in Nutraceutical Industry:
Galactinol Dihydrate is used as an ingredient in the development of nutraceutical products aimed at promoting overall health and well-being. Its role in serotonin activity and the breakdown of fats and cholesterol reduction makes it a beneficial addition to supplements and functional foods.
Used in Research and Development:
Galactinol Dihydrate is used as a research tool for studying the mechanisms behind various biological processes, such as insulin signal transduction and membrane potentials. Its presence in these processes allows scientists to gain a deeper understanding of the underlying molecular interactions and develop targeted therapies for various diseases.
Used in Cosmetics Industry:
Galactinol Dihydrate can be used as an active ingredient in the development of cosmetics and skincare products. Its role in nerve guidance and cytoskeleton assembly may contribute to the development of products that promote skin health and regeneration.

Check Digit Verification of cas no

The CAS Registry Mumber 3687-64-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,8 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3687-64:
(6*3)+(5*6)+(4*8)+(3*7)+(2*6)+(1*4)=117
117 % 10 = 7
So 3687-64-7 is a valid CAS Registry Number.

3687-64-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name α-D-galactosyl-(1→3)-1D-myo-inositol

1.2 Other means of identification

Product number -
Other names Galactinol hydrate

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:3687-64-7 SDS

3687-64-7Relevant articles and documents

Creation of an α-mannosynthase from a broad glycosidase scaffold

Yamamoto, Keisuke,Davis, Benjamin G.

supporting information; experimental part, p. 7449 - 7453 (2012/09/21)

α-Mannosides made easy: Mutation of a family-GH31 α-glucosidase that displays plasticity to alterations at the 2-OH position of donor substrates created an efficient α-mannoside-synthesizing biocatalyst. A simple fluoride donor reagent was used for the synthesis of a range of mono-α-mannosylated conjugates using the α-mannosynthase displaying low (unwanted) oligomerization activity. Copyright

Syntheses of penta-O-benzyl-myo-inositols, O-β-L-arabinosyl-(1 → 2)sn-myo-inositol, O-α-D-galactosyl-(1 → 3)-sn-myo-inositol, and O-α-D-galactosyl-(1 → 6)-O-α-D-galactosyl-(1 → 3)-sn-myo-inositol

Koto,Hirooka,Yoshida,Takenaka,Nagamitsu,Sakurai,Zen,Yago,Tomonaga

, p. 2521 - 2529 (2007/10/03)

Two-step conversions of myo-inositol into (±)-2,3,4,5,6- and 1,3,4,5,6-penta-O-benzyl-myo-inositols are described. Starting from these monohydroxy derivatives of myo-inositol, O-β-L-arabinopyranosyl-(1→2)-sn-myo-inositol from Japanese green tea, Camellia sinensis, and O-α-D-galactopyranosyl-(1→3)-sn-myo-inositol (galactinol) as well as its homolog, O-α-D-galactopyranosyl-(1→6(II))-galactinol, were synthesized by way of the in situ activating glycosylation procedure.

Biosynthesis of mannophospholipids by Mycobacterium phlei.

Hill,Ballou

, p. 895 - 902 (2007/10/04)

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