13259-51-3 Usage
Type of Compound
Synthetic chemical compound
Relation to DDT
Deuterated form of DDE, a breakdown product of the pesticide DDT
Application
Used as an analytical standard in environmental and biological studies to track the presence and behavior of DDE in various samples
Chemical Structure
Highly chlorinated compound with three chlorine atoms and two phenyl rings
Environmental Persistence
Highly persistent in the environment due to its chemical structure
Bioaccumulative Properties
Potential for bioaccumulation in organisms
Isotopic Composition
Stable isotopic composition, making it suitable for tracer studies
Use in Tracer Studies
Investigates the transport and fate of DDE in ecosystems
Classification
Considered a persistent organic pollutant (POP)
Health and Environmental Concerns
Potential adverse effects on human health and the environment
Check Digit Verification of cas no
The CAS Registry Mumber 13259-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,5 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13259-51:
(7*1)+(6*3)+(5*2)+(4*5)+(3*9)+(2*5)+(1*1)=93
93 % 10 = 3
So 13259-51-3 is a valid CAS Registry Number.
13259-51-3Relevant articles and documents
N-Alkenylporphyrins from the Reaction of DDT with Chloroiron(III) Tetraphenylporphine and Iron Powder
Castro, C. E.,Wade, R. S.
, p. 5342 - 5351 (1985)
The reaction of DDT with chloroiron(III) tetraphenylporphine and a large excess of iron powder in 9:1 methylene chloride-methanol produces a mixture of porphyrin products.Demetalation of the product solution under argon yields DDD, tetraphenylporphine, N-tetraphenylporphyrin ("N-vinyl"), and the monocation of N21,N22-tetraphenylporphine ("Rhodo").The alleged "vinylidene carbene" of DDT reported to be generated in this reaction and its reversibly obtained one-electron oxidation product are shown by several means including demetalation and synthesis to be iron(II) and iron(III) complexes of N-vinylporphyrin.The diamagnetic nature of the iron(II) porphyrin(II) porphyrin and, in part, its unusual stability to air are explained by back (?) bonding of the metal to the adjacent olefinic linkage.The iron(III) complex of N-vinyl is converted to the bridged Rhodo porphyrin by Lewis acids and reagents capable of polarizing the nitrogen-bound olefin.
