Detail of "3691-35-8"
- MSDS Download

- CAS Number:
- 3691-35-8
- Name:
1H-Indene-1,3(2H)-dione,2-[2-(4-chlorophenyl)-2-phenylacetyl]-
- Superlist Name:
- Chlorphacinon
- Molecular Structure:
![Molecular Structure of 3691-35-8 (1H-Indene-1,3(2H)-dione,2-[2-(4-chlorophenyl)-2-phenylacetyl]-)](http://www.lookchem.com/300w/2010/0621/3691-35-8.jpg)
- Formula:
- C23H15 Cl O3
- Molecular Weight:
- 374.83
- Synonyms:
- 1,3-Indandione,2-[(p-chlorophenyl)phenylacetyl]- (7CI,8CI); 1H-Indene-1,3(2H)-dione, 2-[(4-chlorophenyl)phenylacetyl]-(9CI); 2-Acetyl-2-(p-chlorophenyl)-2-phenylindan-1,3-dione;2-Phenyl-p-chlorophenylacetyl-1,3-indandione;2-[(p-Chlorophenyl)phenylacetyl]-1,3-indandione;2-[2-Phenyl-2-(4-chlorophenyl)acetyl]-1,3-indandione; Caid; Chlorodiphacinone;Chlorophacinon; Chlorophacinone; Chlorphacinone; Chlorphenacone; Drat; Kaid; LM91; Liphadione; Raticide; Raticide-Caid; Ratindan 3; Redentin; Rozol
- EINECS:
- 223-003-0
- Melting Point:
- 140-144℃
- Appearance:
- white or almost white powder
- Hazard Symbols:


- Risk Codes:
- R23;R27/28;R48/24/25;R50/53
- Safety:
- 36/37-45-60-61 Details
- Transport Information:
- UN 2811

1H-Indene-1,3(2H)-dione,2-[2-(4-chlorophenyl)-2-phenylacetyl]-
![Molecular Structure of 3691-35-8 (1H-Indene-1,3(2H)-dione,2-[2-(4-chlorophenyl)-2-phenylacetyl]-)](http://www.lookchem.com/300w/2010/0621/3691-35-8.jpg)


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Reference
- High-performance liquid chromatographic strategies for the determination and confirmation of anticoagulant rodenticide residues in animal tissues
- High-performance liquid chromatographic strategies for the determination and confirmation of anticoagulant rodenticide residues in animal tissues. Hunter, K. (Agric. Sci. Serv., Dep. Agric. Fish. Scotland, East Craigs/Edinburgh EH12 8NJ, UK). J. Chromatogr., 321(2), 255-72 (English) 1985. CODEN: JOCRAM. ISSN: 0021-9673. DOCUMENT TYPE: Journal CA Section: 5 (Agrochemical Bioregulators) Section cross-reference(s): 4, 80 Residues of warfarin [81-81-2], coumatetralyl [5836-29-3], difenacoum [56073-07-5], brodifacoum [56073-10-0], bromadiolone [28772-56-7], diphacinone [82-66-6], and chlorophacinone [3691-35-8] in animal tissues were extd. with CHCl3-MeCO (1:1, vol./vol.). Exts. were cleaned-up by an integrated gel permeation and adsorption chromatog. procedure which divided the rodenticides into 2 groups. Residues were then detd. and confirmed using normal-phase, ion-pair and weak ion-exchange HPLC techniques. Ion-pair gradient sepn. resolved all 7 rodenticides in a single chromatog. anal. UV detection methods were employed for all 7 rodenticides. Use of a diode array detection system permitted addnl. confirmation of residues down to 0.1 mg/kg by matching UV spectra and derivs. of spectra. Sensitive fluorescence detection was possible for the coumarin-based rodenticides, but not for diphacinone and chlorophacinone. Post-column pH-switching fluorescence detection methods were superior to other methods of fluorescence detection of coumarin-based rodenticides. Recoveries from spiked liver tissue were around 90% at levels from 0.05 to 1 mg/kg. Detection limits of around 0.002 mg/kg for most rodenticides and of 0.01 mg/kg for warfarin could be achieved with animal tissue exts.
- Effect of humic acids on the acute toxicity of selected pesticides
- Effect of humic acids on the acute toxicity of selected pesticides. Golbs, Siegfried; Kuehnert, M.; Fuchs, V. (WB Pharmakol., Pharm. Toxikol., Karl-Marx-Univ., Leipzig DDR-7010, Ger. Dem. Rep.). Z. Gesamte Hyg. Ihre Grenzgeb., 30(12), 720-3 (German) 1984. CODEN: ZHYGAM. ISSN: 0049-8610. DOCUMENT TYPE: Journal CA Section: 4 (Toxicology) Oral administration of parathion-methyl [298-00-0], lindane (I) [58-89-9], chlorophacinone [3691-35-8], or carbaryl [63-25-2] (LD50) with 500 mg humic acids/kg decreases the pesticide toxicities by 76-81, 42-56, 49-80, and 10-19%, resp. Acetylcholinesterase [9000-81-1] activity in blood decreased after chronic administration of 6-12 mg parathion-methyl/kg daily and improved or normalized when the pesticide was administered with 200 mg; changes in blood serum proteins also normalized. Warfarin [81-81-2] (LD50) was detoxified by 500 mg humic acids/kg/day. Mechanisms are discussed of the protective effects of humic acids against pesticide poisoning.

