2315-67-5 Usage
Description
OCTOXYNOL-3 is a pale yellow oil that is a common environmental pollutant exhibiting weak estrogenic effects. It has been found to cause harm to the male reproductive system of vertebrates, particularly in aquatic species, where it has been observed to cause gonadal intersex, altered sex ratios, and reduced gonad size.
Uses
Used in Environmental Studies:
OCTOXYNOL-3 is used as a research subject for studying its impact on the male reproductive system of vertebrates, particularly in aquatic species. The application reason is to understand the effects of this environmental pollutant on gonadal intersex, altered sex ratios, and reduced gonad size, which can help in developing strategies to mitigate its harmful effects on aquatic life and ecosystems.
Check Digit Verification of cas no
The CAS Registry Mumber 2315-67-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,1 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2315-67:
(6*2)+(5*3)+(4*1)+(3*5)+(2*6)+(1*7)=65
65 % 10 = 5
So 2315-67-5 is a valid CAS Registry Number.
2315-67-5Relevant articles and documents
Isolation of bacterial strains that produce the endocrine disruptor, octylphenol diethoxylates, in paddy fields
Nishio, Eriko,Ichiki, Yayoi,Tamura, Hiroto,Morita, Shiro,Watanabe, Katuji,Yoshikawa, Hiromichi
, p. 1792 - 1798 (2002)
Topsoil samples were collected from 36 different paddy fields in West Japan. Each soil sample was incubated with a basal salt-medium containing 0.2% OPPEO. Twelve samples possessed OPPEO-degrading activity, from which twelve cultures of OPPEO-degrading ba
Method for preparing arylpoly(oxyalkyl) amines
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Page/Page column 4, (2010/11/30)
The invention pertains to a process for preparing an arylpoly(oxyalkyl)compound, wherein the process involves reacting a phenol with a halohydrin, and reacting the reaction product with an amino alkyl halide. The invention seeks to provide a less hazardous alternative to conventional preparation processes where arylpoly(oxyalkyl)compounds are made starting from an extremely toxic and hazardous dihalogeno-polyalkylene ether. The preferred arylpoly(oxyalkyl)compound is benzethonium chloride.