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81025-03-8

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81025-03-8 Usage

Description

(2S,3R,4R,5R)-4-[(2R,3R,4S,5R,6S)-3,4,5,6-tetrahydroxytetrahydro-2H-pyran-2-yl]oxyhexane-1,2,3,5,6-pentol dihydrate (non-preferred name) is a complex organic compound with a hexane backbone and a tetrahydroxytetrahydro-2H-pyran-2-yl group linked through an oxy linkage. It is a highly hydrophilic and water-soluble molecule, characterized by its multiple hydroxyl (OH) groups and the presence of a dihydrate. The specific stereochemistry of the compound is indicated by the letters S and R, which denote the spatial orientation of the substituent groups around the chiral centers of the molecule.

Uses

Used in Pharmaceutical Industry:
(2S,3R,4R,5R)-4-[(2R,3R,4S,5R,6S)-3,4,5,6-tetrahydroxytetrahydro-2H-pyran-2-yl]oxyhexane-1,2,3,5,6-pentol dihydrate (non-preferred name) is used as a pharmaceutical compound for its potential therapeutic applications. Its hydrophilic nature and multiple hydroxyl groups may allow for interactions with various biological targets and contribute to its efficacy in treating certain conditions.
Used in Cosmetic Industry:
In the cosmetic industry, (2S,3R,4R,5R)-4-[(2R,3R,4S,5R,6S)-3,4,5,6-tetrahydroxytetrahydro-2H-pyran-2-yl]oxyhexane-1,2,3,5,6-pentol dihydrate (non-preferred name) is used as a humectant to help retain moisture in skincare products. Its water-soluble properties and ability to form hydrogen bonds with water molecules make it an effective ingredient for maintaining skin hydration and improving skin texture.
Used in Food Industry:
(2S,3R,4R,5R)-4-[(2R,3R,4S,5R,6S)-3,4,5,6-tetrahydroxytetrahydro-2H-pyran-2-yl]oxyhexane-1,2,3,5,6-pentol dihydrate (non-preferred name) is used in the food industry as a humectant to improve the texture and shelf life of various food products. Its ability to retain moisture and prevent crystallization can be beneficial in confectionery, baked goods, and other food items that require controlled moisture content.
Used in Chemical Research:
In the field of chemical research, (2S,3R,4R,5R)-4-[(2R,3R,4S,5R,6S)-3,4,5,6-tetrahydroxytetrahydro-2H-pyran-2-yl]oxyhexane-1,2,3,5,6-pentol dihydrate (non-preferred name) serves as a model compound for studying the properties and behavior of complex organic molecules. Its unique stereochemistry and hydrophilic nature make it an interesting subject for research in organic chemistry, supramolecular chemistry, and related fields.

Check Digit Verification of cas no

The CAS Registry Mumber 81025-03-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,0,2 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 81025-03:
(7*8)+(6*1)+(5*0)+(4*2)+(3*5)+(2*0)+(1*3)=88
88 % 10 = 8
So 81025-03-8 is a valid CAS Registry Number.

81025-03-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3R,4R,5R)-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexane-1,2,3,5,6-pentol,dihydrate

1.2 Other means of identification

Product number -
Other names Lactitol dihydrate

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:81025-03-8 SDS

81025-03-8Upstream product

81025-03-8Downstream Products

81025-03-8Relevant articles and documents

Method of preparing lacitol monohydrate and dihydrate

-

, (2008/06/13)

The invention relates to the new product lactitol monohydrate and to a method for the production of crystalline lactitol. The crystalline lactitol monohydrate can be obtained bij seeding an aqueous lactitol solution of a special concentration under special conditions causing the lactitol monohydrate to crystallize and recovering the product. From the mother liquor a further amount of lactitol dihydrate can be recovered. Crystalline lactitol dihydrate can be obtained using different special conditions. Lactitolmonohydrate can further be obtained by mixing one part bij weight of an aqueous lactitol solution of a suited concentration with 1 tot 3 parts bij weight of methanol or ethanol and cooling the mixture to 15° tot 25° C.

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