13002-16-9 Usage
General Description
1,1-Diisobutoxybutane is a chemical compound with the molecular formula C12H26O2. It is a colorless liquid with a boiling point of 205-207°C and is primarily used as a solvent and a processing aid in various industries. This chemical is known for its low volatility, low toxicity, and high solvency power, making it suitable for use in coatings, adhesives, and other industrial applications. It is also used as a component in some specialty fuels and as a plasticizer in polymer formulations. 1,1-Diisobutoxybutane is considered to be relatively safe for use, but proper handling and storage procedures should be followed to minimize any potential risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 13002-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,0 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13002-16:
(7*1)+(6*3)+(5*0)+(4*0)+(3*2)+(2*1)+(1*6)=39
39 % 10 = 9
So 13002-16-9 is a valid CAS Registry Number.
13002-16-9Relevant articles and documents
CATALYSED LIQUID PHASE OXIDATION OF ACETALS BY MOLECULAR OXYGEN
Vcelak, Jaroslav,Klimova, Miroslava,Chvalovsky, Vaclav
, p. 847 - 866 (2007/10/02)
Nine different acetals have been oxidized in the presence of Co(OOCCH3)2*4H2O under isobaric conditions (0.1 - 0.2 MPa O2) while following the uptake of molecular oxygen.The reactivity of acetals was expressed by the rate constants of the autocatalytic model of oxidation.The main product of the oxidation are alcohols, esters and acids.The distribution of products and the total reactivity of acetals are controlled by the structure of both parts of acetal molecule.The dominant effects of the course of the reaction exerts the type of carbon atoms on which radicals are formed.The oxidation is accompanied by consecutive and co-oxidation reactions, by deactivation of the catalysts and by decarbonylation of intermediate products.The effect of oxygen pressure is reported and the more detailed radical mechanism of the oxidation is proposed.
