39801-14-4 Usage
Description
Photomirex is a toxic metabolite and a photodegradation product of the insecticide Mirex. It is a white solid that has been identified as an environmental contaminant in various ecosystems, including Great Lakes fish, soil, and human adipose tissue.
Uses
Used in Environmental Studies:
Photomirex is used as a subject of study in environmental science for understanding its impact on ecosystems and human health. The presence of photomirex in various environmental samples, such as fish, soil, and human adipose tissue, highlights the need for further research on its distribution, persistence, and potential risks.
Used in Regulatory Frameworks:
Photomirex is used as a reference point in regulatory frameworks and guidelines for environmental protection. Its identification as a contaminant in various ecosystems has led to the development of policies and regulations aimed at controlling the release and spread of such toxic substances.
Used in Public Health Initiatives:
Photomirex is used as a focal point in public health initiatives to raise awareness about the potential risks associated with environmental contaminants. Efforts are made to educate the public on the importance of reducing exposure to such substances and promoting a cleaner environment.
Used in Industrial Monitoring:
Photomirex is used as a parameter in industrial monitoring to ensure compliance with environmental regulations and to prevent contamination of natural resources. Industries that may be associated with the production or use of Mirex or its derivatives are required to monitor and control the release of photomirex into the environment.
Used in Toxicology Research:
Photomirex is used as a subject of interest in toxicology research to study its effects on living organisms and to develop methods for its detection, quantification, and mitigation. Understanding the toxicological profile of photomirex is crucial for assessing its potential risks and developing strategies for its management and control.
Safety Profile
Poison by ingestion.
Experimental teratogenic effects.
Questionable carcinogen with experimental
tumorigenic data. Mutation data reported. When heated to decomposition it emits
toxic fumes of Cl-.
Check Digit Verification of cas no
The CAS Registry Mumber 39801-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,8,0 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 39801-14:
(7*3)+(6*9)+(5*8)+(4*0)+(3*1)+(2*1)+(1*4)=124
124 % 10 = 4
So 39801-14-4 is a valid CAS Registry Number.
InChI:InChI=1/C10HCl11/c11-2-1-3(12)5(14)4(1,13)10(20,21)7(2,16)8(5,17)6(2,15)9(3,18)19/h1H
39801-14-4Relevant articles and documents
Binding effects on humic-mediated photoreaction: Intrahumic dechlorination of mirex in water
Burns, Susan E.,Hassett, John P.,Rossp, Maura V.
, p. 2934 - 2941 (1996)
A kinetic model was developed describing the effects of hydrophobic partitioning to humics on second-order humic-mediated photoreactions in aqueous solution. Model development and evaluation were in terms of the humic-mediated dechlorination of the hydrophobic chlorocarbon, mirex. Mirex dechlorination in irradiated (λ ≤ 290 nm) Aldrich humic acid (HA) solution was examined as a function of humic acid and scavenger concentration. Kinetic models in which HA solution is described as a homogeneous or single-phase solution were not able to describe the effects of HA and scavenger concentrations on mirex dechlorination rates. However, these effects were successfully described by including partitioning in the models to characterize the bound phase and dissolved phase mirex reactions separately. The resulting model uses homogeneous phase kinetics to describe reaction in the dissolved phase. Bound phase reaction is described as occurring within individual HA molecules with the distribution of scavengers within HA molecules following a Poisson distribution. Used to assess the relative reactivities of the bound and dissolved phases, the model indicated that the reaction of mirex in HA solution is confined to the humic phase. The general predictions and utility of the model are evaluated both in terms of experimental data and pollutant photodegradation.
Alley et al.
, p. 442,444 (1974)
