1213-29-2 Usage
Uses
Used in Water Treatment:
Phosphonic acid, [3-(2-methyl-1,3-dioxolan-2-yl)propyl]-, diethyl ester is used as a chelating agent for preventing scale formation in water systems. Its ability to bind to metal ions helps maintain the efficiency and longevity of water treatment processes.
Used in Metal Finishing:
In the metal finishing industry, GDPD is utilized as a chelating agent to improve the quality and uniformity of metal surfaces. It helps in removing impurities and promoting a smooth, corrosion-resistant finish.
Used in Detergent Applications:
Phosphonic acid, [3-(2-methyl-1,3-dioxolan-2-yl)propyl]-, diethyl ester is used as a chelating agent in detergent formulations to enhance their cleaning performance. It helps in binding and removing metal ions, thus preventing the formation of stains and deposits.
Used in Metalworking Fluids:
GDPD is employed as a stabilizer and corrosion inhibitor in metalworking fluids. Its properties help in extending the life of the fluids and protecting metal surfaces from corrosion during machining processes.
Used in Agricultural Formulations:
Phosphonic acid, [3-(2-methyl-1,3-dioxolan-2-yl)propyl]-, diethyl ester is used as a dispersant in agricultural formulations. It helps in improving the distribution and effectiveness of agrochemicals, ensuring optimal crop protection and yield.
Check Digit Verification of cas no
The CAS Registry Mumber 1213-29-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1213-29:
(6*1)+(5*2)+(4*1)+(3*3)+(2*2)+(1*9)=42
42 % 10 = 2
So 1213-29-2 is a valid CAS Registry Number.
1213-29-2Relevant academic research and scientific papers
Synthesis of labelled [13C6]testosterone and [13C5]19-nortestosterone
Joubert,Beney,Marsura,Luu-Duc
, p. 745 - 754 (2007/10/02)
The condensation of ethyl acetoacetate-13C4 and ethyl bromoacetate-13C2 afforded, in seven steps, (1,2,3,4,5-13C5) 5-(diethylphosphono)-2-pentanone ethylene ketal 9. The reaction of this labelled compound with 7-[[(1,1-dimethylethyl)-dimethylsilyl]oxy]-1,6,6a,7,8, 9, 9a, 9b-octahydro-6a-methyl-[6aS-(6aa,7a,9aβ,9ba)] cyclopenta[f][1]benzopyran-3 (2H)-one 13 gave the benzindenone 14 which was converted to (1,2,3,4,10,19-13C6)testosterone 17 then, into (1,2,3,4,10-13C5)19-nortestosterone 18 by a reductive alkylation method.
