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1,3-DIOXANE-5,5-DIMETHANOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6228-25-7

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6228-25-7 Usage

Uses

1,3-Dioxane-5,5-dimethanol can be used to produce composition for flexible structure.

Check Digit Verification of cas no

The CAS Registry Mumber 6228-25-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,2 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6228-25:
(6*6)+(5*2)+(4*2)+(3*8)+(2*2)+(1*5)=87
87 % 10 = 7
So 6228-25-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O4/c7-1-6(2-8)3-9-5-10-4-6/h7-8H,1-5H2

6228-25-7 Well-known Company Product Price

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  • Aldrich

  • (220620)  1,3-Dioxane-5,5-dimethanol  90%, technical grade

  • 6228-25-7

  • 220620-25G

  • 3,031.47CNY

  • Detail

6228-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [5-(hydroxymethyl)-1,3-dioxan-5-yl]methanol

1.2 Other means of identification

Product number -
Other names 1,3-Dioxane-5,5-dimethanol

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:6228-25-7 SDS

6228-25-7Relevant academic research and scientific papers

TRANSACETALISATION DE TRIOLS A PARTIR DU DIMETHOXYMETHANE. SELECTIVITE ET APPLICATIONS SYNTHETIQUES

Gras, Jean-Louis,Nouguier, Robert,Mchich, Mohammed

, p. 6601 - 6604 (2007/10/02)

THe LiBr assisted/acid catalyzed transacetalation of triols from DMM affords a highly selective method for the synthesis of hydroxy compounds bearing a dioxane ring.These compounds might further conveniently be alkylated by phase transfer catalyzis.

Derivatives of Pentaerythritol, I. - Formaldehyde Bis(pentaerythrityl) Acetal and Tetrapentaerythritol

Werle, Peter,Nonnenmacher, Gerhard,Kruse, Karsten

, p. 938 - 945 (2007/10/02)

Pure formaldehyde bis(pentaerythrityl) acetal (9) and tetrapentaerythritol (4) were isolated for the first time as by-products during the synthesis of pentaerythritol from acetaldehyde and formaldehyde.The spectra show that 4 is not a branched molecule as suggested but a straight-chained one.

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