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4704-99-8

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4704-99-8 Usage

Description

2-(HydroxyMethyl)-2-phenylpropane-1,3-diol, also known as Glycerol, is a simple polyol compound that is a colorless, viscous liquid. It is a trihydric alcohol with three hydroxyl groups attached to a three-carbon chain, which gives it unique properties and a wide range of applications across various industries.

Uses

Used in Organic Synthesis:
2-(HydroxyMethyl)-2-phenylpropane-1,3-diol is used as a versatile building block in organic synthesis for the production of various chemicals and compounds. Its ability to form esters and ethers makes it a valuable intermediate in the synthesis of a wide range of organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(HydroxyMethyl)-2-phenylpropane-1,3-diol is used as a humectant and solvent in the formulation of various drugs and medications. Its ability to retain moisture and mix with other substances makes it an essential component in the development of pharmaceutical products.
Used in Cosmetics and Personal Care Industry:
2-(HydroxyMethyl)-2-phenylpropane-1,3-diol is used as a moisturizing agent in cosmetics and personal care products. Its humectant properties help to maintain the skin's natural moisture balance, making it a popular ingredient in skincare products, hair care products, and other personal care items.
Used in Food Industry:
In the food industry, 2-(HydroxyMethyl)-2-phenylpropane-1,3-diol is used as a humectant, emulsifier, and sweetener. It helps to retain moisture in food products, improve texture, and extend shelf life. It is commonly found in the production of confectionery, baked goods, and other food items.
Used in Industrial Applications:
2-(HydroxyMethyl)-2-phenylpropane-1,3-diol is used as a component in the manufacturing of various industrial products, such as antifreeze, lubricants, and hydraulic fluids. Its unique properties make it suitable for a wide range of applications in the industrial sector.
Used in Energy Storage:
2-(HydroxyMethyl)-2-phenylpropane-1,3-diol is used as a component in the development of advanced energy storage systems, such as lithium-ion batteries. Its ability to form stable complexes with metal ions makes it a promising candidate for improving the performance and safety of energy storage devices.

Check Digit Verification of cas no

The CAS Registry Mumber 4704-99-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4704-99:
(6*4)+(5*7)+(4*0)+(3*4)+(2*9)+(1*9)=98
98 % 10 = 8
So 4704-99-8 is a valid CAS Registry Number.

4704-99-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name α,α,α-Tris(hydroxymethyl)toluene

1.2 Other means of identification

Product number -
Other names 2-(hydroxymethyl)-2-phenylpropane-1,3-diol

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:4704-99-8 SDS

4704-99-8Relevant articles and documents

EFFICIENT PROCESS FOR MAKING 6-CARBOXY BENZOXAZOLE DERIVATIVES

-

Page/Page column 24-25, (2021/06/26)

The present invention is directed to an efficient process for preparing benzoxazole derivatives comprising the step of reacting a 4-Amino-3-hydroxybenzoic acid compound of Formula III with a 3,5-Dichlorophenyl ortho ester compound of Formula II to provide the compound of Formula I wherein R1, R2a, R2b and R2c are as described herein.

Multypodal tethers for high-density attachment of redox-active moieties to substrates

-

, (2008/06/13)

This invention provides redox-active molecules attached to polypodal (e.g., bipodal, tripodal, quadrapodal, pentapodal, etc.) tethers that can be used for attachment of the redox-active molecules to a substrate (e.g., an electrode). The tethered redox-active molecules are useful for the fabrication of memory devices.

Trivalent cluster mannosides with aromatic partial structure as ligands for the type 1 fimbrial lectin of Escherichia coli

R?ckendorf, Niels,Sperling, Oliver,Lindhorst, Thisbe K.

, p. 87 - 93 (2007/10/03)

Mannose-specific adhesion of E. coli bacteria to their host cells is mediated by so-called type 1 fimbriae containing lectin domains present on the type 1 fimbrial FimH protein. The crystal structure of a FimH-FimC(chaperone) protein complex revealed a nu

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