16456-56-7 Usage
Uses
Used in Lubricants, Polymers, and Coatings:
Butyl hydrogen phosphonate is used as an additive for its high thermal stability and resistance to oxidation, enhancing the performance and durability of lubricants, polymers, and coatings.
Used in Flame Retardants:
Butyl hydrogen phosphonate is used as a component in the production of flame retardants, contributing to the fire safety of various materials.
Used in Water Treatment Processes:
Butyl hydrogen phosphonate is used as a corrosion inhibitor in water treatment processes, protecting metal surfaces from corrosion and extending the life of equipment.
Used in Metal Ion Extraction Processes:
Butyl hydrogen phosphonate is used as a chelating agent in metal ion extraction processes, facilitating the separation and recovery of metal ions from various sources.
Used in Pharmaceutical Formulations:
Butyl hydrogen phosphonate is used as a component in some pharmaceutical formulations, potentially contributing to the development of new drugs and therapies.
Used in the Development of New Materials and Technologies:
Due to its unique properties and applications, butyl hydrogen phosphonate has garnered interest for its potential use in the development of innovative materials and technologies, further expanding its range of applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 16456-56-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,5 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16456-56:
(7*1)+(6*6)+(5*4)+(4*5)+(3*6)+(2*5)+(1*6)=117
117 % 10 = 7
So 16456-56-7 is a valid CAS Registry Number.
InChI:InChI=1/C4H11O3P/c1-2-3-4-7-8(5)6/h8H,2-4H2,1H3,(H,5,6)
16456-56-7Relevant academic research and scientific papers
Process for making a plant growth regulator
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Page/Page column 6, (2008/06/13)
A method for making a plant growth regulator includes the step of reacting vinyl chloride with a phosphorous reagent.
CONVENIENT SYNTHETIC ROUTE TO MONO- OR DIAKLYL PHOSPHATE FROM INORGANIC PHOSPHORUS ACIDS
Okamoto, Yoshiki,Kusano, Tetuya,Takamuku, Setsuo
, p. 195 - 200 (2007/10/02)
Mono- or dialkyl phosphate was synthesized in a favorable yield by oxidation of phosphonic or phosphinic acid in alcohol with oxygen at the presence of a catalytic amount of copper(II)chloride.The reaction may proceed via the formation of corresponding phosphorochloridate or phosphorochloridite.
Degradation of n-Butylaminocyclohexyl phosphonic Acid di-n-Butylester (Buminafos) in Aqueous Medium
Schneider, B.,Porzel, A.,Weidhase, R.,Schuette, H. R.
, p. 85 - 90 (2007/10/02)
In aqueous medium, breakdown of Buminafos (1) is connected with total loss of its herbicidal activity.The phosphorus-carbon bond is cleaved and n-butylcyclohexylidene amine (3), cyclohexanone (5), phosphoric acid mono-n-butyl ester (4) (partly as n-butylamine salt), and 1-aminocyclohexyl phosphonic acid di-n-butylester (8) were found as degradation products of carbon-14 labeled Buminafos.Identification was performed by MS, GC/MS, 1H- and 31P-n.m.r. spectroscopy, by detection of phosphorus, and by means of the radioactivity.
