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2,2,4,6-Tetramethyl-1,3-dioxane, also known as p-menthane-3,8-diol or PMD, is a colorless, volatile, and highly flammable liquid with a distinctive camphor-like odor. It is an organic compound belonging to the dioxane family, characterized by a cyclic ether structure with four methyl groups attached to the carbon atoms. This chemical is primarily used as a solvent, particularly in the production of fragrances, flavors, and essential oils. It is also employed as a stabilizer in the synthesis of other chemicals and as a component in various industrial processes. Due to its potential health risks, including irritation to the eyes, skin, and respiratory system, as well as its classification as a possible carcinogen, it is crucial to handle 2,2,4,6-tetramethyl-1,3-dioxane with proper safety measures and in accordance with regulatory guidelines.

17227-17-7

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17227-17-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17227-17-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,2 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17227-17:
(7*1)+(6*7)+(5*2)+(4*2)+(3*7)+(2*1)+(1*7)=97
97 % 10 = 7
So 17227-17-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O2/c1-6-5-7(2)10-8(3,4)9-6/h6-7H,5H2,1-4H3

17227-17-7SDS

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 cis-2,2,4,6-Tetramethyl-1,3-dioxane

1.2 Other means of identification

Product number -
Other names -

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:17227-17-7 SDS

17227-17-7Relevant academic research and scientific papers

Mild and efficient protection of diol and carbonyls as cyclic acetals catalysed by iron (III) chloride

Karamé, Iyad,Alamé, Mohamad,Kanj, Ali,Baydoun, Ghinwa Nemra,Hazimeh, Hassan,El Masri, Mirvat,Christ, Lorraine

experimental part, p. 525 - 529 (2012/05/19)

A friendly method for the protection of diols and carbonyls catalysed by hexahydrated iron (III) chloride has been developed. This method, which consists of the transformation of diols and carbonyls to cyclic acetals, functions in mild conditions and it is efficient for a wide range of diols.

Selective radical-chain epimerisation at C-H centres α to oxygen under conditions of polarity-reversal catalysis

Dang, Hai-Shan,Roberts, Brian P.

, p. 4271 - 4274 (2007/10/03)

Polarity-reversal catalysis by tri-tert-butoxysilanethiol has been applied to promote radical-chain epimerisation selectively at carbon centres of the type R1R2C*(H)OR.

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