183-03-9 Usage
Description
1,4-Dioxaspiro[4.7]dodecane, also known as p-Dioxane, is a cyclic organic compound with the molecular formula C10H18O2. It features a unique spiro structure, with a dioxane ring fused to a dodecane chain.
Uses
Used in Chemical Industry:
1,4-Dioxaspiro[4.7]dodecane is used as a solvent for the formulation of specialty inks, adhesives, and coatings due to its ability to dissolve a wide range of substances and its compatibility with various materials.
Used in Perfumery and Personal Care Products:
1,4-Dioxaspiro[4.7]dodecane is used as a fragrant ingredient in perfumes and personal care products, providing a pleasant scent and enhancing the overall sensory experience of these products.
Safety Precautions:
1,4-Dioxaspiro[4.7]dodecane is flammable and may be harmful if inhaled, ingested, or absorbed through the skin. Therefore, it requires careful handling and storage to prevent accidents and ensure the safety of workers and consumers. Additionally, it has been shown to have low acute toxicity in animal studies, which should be taken into consideration when assessing its safety for human use.
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.
183-03-9Relevant 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.
