15067-26-2 Usage
Uses
Used in Pesticide Analysis:
Acenaphthene-d10 is used as an internal standard for the determination of pesticides in rice samples. It is employed in conjunction with a suitable multi-residue method, such as the quick, easy, cheap, effective, rugged, and safe (QuEChERS) sample preparation method, combined with gas chromatography coupled with mass spectrometry analysis. This application takes advantage of its stability and compatibility with the analytical technique to ensure accurate and reliable results.
Used in Environmental Analysis:
Acenaphthene-d10 is also used as a polycyclic aromatic hydrocarbon (PAH) surrogate in the analysis of PAHs in various environmental samples, such as soil, river water, and sediments. It is utilized in gas chromatography coupled with mass spectrometry (GC-MS) to monitor and quantify the presence of PAHs, which are known to be harmful pollutants. The use of Acenaphthene-d10 as a surrogate aids in the accurate quantification and assessment of PAH contamination in the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 15067-26-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,6 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15067-26:
(7*1)+(6*5)+(5*0)+(4*6)+(3*7)+(2*2)+(1*6)=92
92 % 10 = 2
So 15067-26-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H10/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-6H,7-8H2/i1D,2D,3D,4D,5D,6D,7D2,8D2
15067-26-2Relevant articles and documents
Efficient H-D exchange of aromatic compounds in near-critical D2O catalysed by a polymer-supported sulphonic acid
Boix, Carmen,Poliakoff, Martyn
, p. 4433 - 4436 (2007/10/03)
Hydrogen atom exchange of aromatic compounds in neutral near-critical D2O has been improved by using a polymer-supported sulphonic acid catalyst. Phenol, aniline, quinoline, and substituted aromatic hydrocarbons are selectively ring-perdeuterated in high yields with insignificant by-product formation at 325 °C for 24 h in D2O/Deloxan.
