3903-88-6 Usage
Chemical structure
1-(pentylperoxy)pentane is an organic peroxide compound with a five-carbon chain and a peroxy group attached to one of the carbon atoms.
Functional group
The peroxy group (-O-O-) is the key functional group in 1-(pentylperoxy)pentane, which contributes to its reactivity.
Reactivity
Due to the presence of the peroxy group, 1-(pentylperoxy)pentane is highly reactive and can initiate various chemical reactions.
Hazards
1-(pentylperoxy)pentane is potentially hazardous due to its tendency to undergo explosive decomposition.
Safety protocols
It is crucial to store and handle 1-(pentylperoxy)pentane with proper safety measures to prevent accidents and ensure its safe use in chemical processes.
Stability
The stability of 1-(pentylperoxy)pentane may be affected by factors such as temperature, pressure, and exposure to other reactive substances.
Storage
It should be stored in a cool, dry, and well-ventilated area, away from heat, sparks, and open flames.
Transportation
When transporting 1-(pentylperoxy)pentane, it is essential to follow specific guidelines and regulations to minimize the risk of accidents.
Disposal
Safe disposal methods should be employed to prevent environmental contamination and potential hazards associated with the decomposition of 1-(pentylperoxy)pentane.
Check Digit Verification of cas no
The CAS Registry Mumber 3903-88-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,0 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3903-88:
(6*3)+(5*9)+(4*0)+(3*3)+(2*8)+(1*8)=96
96 % 10 = 6
So 3903-88-6 is a valid CAS Registry Number.
3903-88-6Relevant articles and documents
The selective functionalization of saturated hydrocarbons. Part 40. Aspects of Fe(II) based peroxide fragmentation in pyridine solution
Barton, Derek H. R.,Launay, Franck
, p. 14565 - 14578 (2007/10/03)
The Haber-Weiss mechanism does not apply to the Fe(II) induced fragmentation of primary and secondary hydroperoxides in pyridine. However, it does apply to tertiary hydroperoxides. Steric bulk is an important factor in Fe(II) induced dialkyl peroxide decomposition in pyridine. On the contrary in tetrahydrofuran a different relatively unhindered electron transfer process predominates where the Fe(II) becomes a catalyst.