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183-03-9

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183-03-9 Usage

General Description

1,4-Dioxaspiro[4.7]dodecane, also known as p-Dioxane, is a chemical compound with the molecular formula C10H18O2. It is a cyclic organic compound with a unique spiro structure, consisting of a dioxane ring fused to a dodecane chain. 1,4-Dioxaspiro[4.7]dodecane is commonly used as a solvent in the chemical industry, particularly in the formulation of specialty inks, adhesives, and coatings. It is also used as a fragrant ingredient in perfumes and personal care products. 1,4-Dioxaspiro[4.7]dodecane is flammable and may be harmful if inhaled, ingested, or absorbed through the skin, warranting careful handling and storage precautions. Additionally, it has been shown to have low acute toxicity in animal studies.

Check Digit Verification of cas no

The CAS Registry Mumber 183-03-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,8 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 183-03:
(5*1)+(4*8)+(3*3)+(2*0)+(1*3)=49
49 % 10 = 9
So 183-03-9 is a valid CAS Registry Number.

183-03-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-Dioxaspiro[4.7]dodecane

1.2 Other means of identification

Product number -
Other names 1,4-dioxaspiro<4.7>dodecane

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:183-03-9 SDS

183-03-9Downstream Products

183-03-9Relevant articles and documents

REACTIONS DE TRANSCETALISATION-III. APPROCHE QUANTITATIVE DE LA SELECTIVITE ET DU RENDEMENT POUR LES MOLECULES DIFONCTIONNELLES.

Bauduin, G.,Bondon, D.,Pietrasanta, Y.,Pucci, B.

, p. 245 - 254 (2007/10/02)

Evidence for an intramolecular transketalization equilibrium in a polyfunctional molecule is described.Using thermodynamic rules, it is possible to establish mathematical equations linking yields with relative ketalization energies and excess of reagent.Experiments with simple compounds are in good agreement with the results obtained from the mathematical model.Thus, for any bifunctional molecule, one can calculate the relative ketalization energy of each function from a simple experiment, and then determine the nature and the excess of the reagent which are necessary to realize the transketalization reaction in the best conditions of yield or selectivity.

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