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6482-32-2

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6482-32-2 Usage

Description

2-(HydroxyMethyl)butane-1,4-diol, also known as D-mannitol or mannitol, is a sugar alcohol derived from glucose. It is a white, crystalline powder with a sweet taste and possesses various therapeutic benefits.

Uses

Used in Food and Beverage Industry:
2-(HydroxyMethyl)butane-1,4-diol is used as a sweetening agent for its sweet taste, enhancing the flavor of various food and beverage products.
Used in Pharmaceutical Formulations:
2-(HydroxyMethyl)butane-1,4-diol is used as an excipient to improve the stability and shelf life of medications, ensuring the quality and effectiveness of pharmaceutical products.
Used in Ophthalmology:
2-(HydroxyMethyl)butane-1,4-diol is used as a medication to reduce pressure inside the eyes, helping to treat glaucoma and other eye conditions.
Used in Nephrology:
2-(HydroxyMethyl)butane-1,4-diol is used to treat certain kidney conditions, supporting kidney function and overall health.
Used as a Diuretic:
2-(HydroxyMethyl)butane-1,4-diol is used to increase urine production, promoting the removal of excess water and salts from the body and aiding in the management of fluid balance.

Check Digit Verification of cas no

The CAS Registry Mumber 6482-32-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,8 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6482-32:
(6*6)+(5*4)+(4*8)+(3*2)+(2*3)+(1*2)=102
102 % 10 = 2
So 6482-32-2 is a valid CAS Registry Number.

6482-32-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Hydroxymethyl)-1,4-butanediol

1.2 Other means of identification

Product number -
Other names 2 - (Hydroxymethyl) - 1,4 - butanediol

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:6482-32-2 SDS

6482-32-2Relevant articles and documents

NANOMATERIALS

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Paragraph 0320; 0321; 0322, (2021/07/17)

Lipid nanoparticle compositions for delivery of nucleic acids are described. In various embodiments the lipid nanoparticle contains an ionizable lipid of the Formula (I). Methods of using such lipid nanoparticle compositions to achieve targeted delivery of therapeutic cargo without the need for a targeting ligand are also provided.

FLAME RETARDANT ITACONIC ACID-BASED COMPOUNDS

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Paragraph 0053, (2019/04/25)

A flame retardant itaconic acid-based compound, a process for forming a flame retardant polymer, and an article of manufacture comprising a material that contains a flame retardant itaconic acid-based polymer are disclosed. The flame retardant itaconic acid-based compound has variable moieties, which include methylene bridge groups, carbonyl groups, vinyl groups, functionalized groups, phenyl-substituted flame retardant groups, and/or functionalized flame retardant groups. The process for forming the flame retardant polymer includes forming a phosphorus-based flame retardant molecule, forming an itaconic acid derivative, chemically reacting the phosphorus-based flame retardant molecule and the itaconic acid derivative to form a flame retardant itaconic acid-based compound, and incorporating the itaconic acid-based flame retardant compound into a polymer to form the flame retardant polymer.

Method for synthesizing 3-tetrahydrofurfuryl alcohol

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Paragraph 0007; 0022, (2017/01/17)

The invention relates to a method for synthesizing 3-tetrahydrofurfuryl alcohol. According to the technical scheme, 2-bromoethanol and diethyl malonate serve as starting materials, under the alkaline condition, 2-hydroxyethyl-diethyl malonate is generated through a reaction, hydrolysis is conducted on the 2-hydroxyethyl-diethyl malonate to generate 2-hydroxyethyl-malonate, catalyzing and high-pressure hydrotreatment are conducted on the 2-hydroxyethyl-malonate to generate 2-hydroxymethyl-1,4-butanediol, and dehydration cyclization is conducted on the 2-hydroxyethyl-1,4-butanediol to generate the 3-tetrahydrofurfuryl alcohol. According to the method for synthesizing the 3-tetrahydrofurfuryl alcohol, the yield can reach over 85 percent, the purity can reach above 95 percent, the reaction condition is mild, the cost is low, operation is easy, and the method has the advantage of being suitable for industrial production.

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