10581-14-3 Usage
Description
Octyl phenyl hydrogen phosphate, also known as 4-(1,1,3,3-tetramethylbutyl)phenol, is a chemical compound that serves as a stabilizer in plastic materials. It is a colorless to pale yellow liquid with a molecular weight of 270.4 g/mol and a boiling point of 249-250 °C.
Uses
Used in Plastic Industry:
Octyl phenyl hydrogen phosphate is used as a stabilizer for plastic materials to improve their thermal stability, prevent degradation from heat and UV radiation, and enhance their mechanical properties.
Used in Rubber Industry:
Octyl phenyl hydrogen phosphate is used as an anti-aging agent in rubber, which helps to extend the lifespan and maintain the quality of rubber products.
Used in Various Industrial Applications:
Octyl phenyl hydrogen phosphate can be found in automotive parts, construction materials, and electrical insulation, where it contributes to the performance and longevity of these products.
Check Digit Verification of cas no
The CAS Registry Mumber 10581-14-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,8 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10581-14:
(7*1)+(6*0)+(5*5)+(4*8)+(3*1)+(2*1)+(1*4)=73
73 % 10 = 3
So 10581-14-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H23O4P/c1-2-3-4-5-6-10-13-17-19(15,16)18-14-11-8-7-9-12-14/h7-9,11-12H,2-6,10,13H2,1H3,(H,15,16)
10581-14-3Relevant articles and documents
REACTIONS DE WITTIG-HORNER ET DE TRANSESTERIFICATION EN UNE OPERATION PAR ACTIVATION ANIONIQUE DE LIAISONS C-H ET O-H EN MILIEU HETEROGENE CARBONATE DE POTASSIUM/ALCOOL
Mouloungui, Z.,Elmestour, R.,Delmas, M.,Gaset, A.
, p. 1219 - 1232 (2007/10/02)
The Wittig-Horner reaction carried out in various alcohols is accompanied by transesterification of the alkyl radical of the α,β-ethylenic ester formed.The occurrence of these two reactions in the same reaction medium is affected by the behavior of: i) the alcohol (solvent and reagent), ii) potassium carbonate (reagent and catalyst).The propensity for the two reactions to occur was found to depend on the polarity of the alcohol.Protic alcohols speeded both the Wittig-Horner and the subsequent transesterification reaction.Both reactions were quantitative despite the use of non-stoichiometric amounts of potassium carbonate.Regeneration in situ of the solid base observed in aprotic medium was markedly enhanced under these reaction conditions.The mechanism proposed for these two reactions incorporates this regeneration process.
