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DIPHACINONE

DIPHACINONE Structure
CAS No.
82-66-6
Chemical Name:
DIPHACINONE
Synonyms
pcq;Ramik;u1363;Didion;Diphac;p.c.q.;Promar;Solvan;u 1363;u-1363
CBNumber:
CB0324612
Molecular Formula:
C23H16O3
Molecular Weight:
340.37
MOL File:
82-66-6.mol
Modify Date:
2024/12/18 13:37:16

DIPHACINONE Properties

Melting point 146-147°
Boiling point 436.18°C (rough estimate)
Density 1.1454 (rough estimate)
vapor pressure 1.37 x l0-8 Pa (25 °C)
refractive index 1.6700 (estimate)
solubility DMSO (Slightly), Methanol (Slightly)
Water Solubility 0.3 mg l-1
pka 2.79±0.10(Predicted)
form Solid
color Light Yellow to Yellow
CAS DataBase Reference 82-66-6(CAS DataBase Reference)
EPA Substance Registry System Diphacinone (82-66-6)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06,GHS08
Signal word  Danger
Hazard statements  H300+H310-H332-H372
Precautionary statements  P264-P280-P301+P310-P302+P350-P310
Hazard Codes  T+
Risk Statements  28-48/23/24/25-24-20
Safety Statements  36/37-45
RIDADR  2811
RTECS  NK5600000
HazardClass  6.1(a)
PackingGroup  I
HS Code  29143990
Hazardous Substances Data 82-66-6(Hazardous Substances Data)
Toxicity LD50 orally (mg/kg): 3 in rats; 340 in mice; 35 in rabbits (Correll)

DIPHACINONE Chemical Properties,Uses,Production

Description

Diphacinone is also called 2-(diphenylacetyl)indan-1,3-dione, is a yellow powder which is practically insoluble in water, readily soluble in chloroform, toluene, xylene, acetone, ethanol, heptane, alkalis [9, p. 431].

Uses

Diphacinone is an anticoagulant rodenticide widely used to control rodent infestations.

Production Methods

Diphacinone is produced by condensation of 1,1-diphenyl acetone with dimethyl phthalate in the presence of sodium methoxide (30).

General Description

Odorless pale yellow crystals. Used as a rodenticide and anticoagulant medication.

Air & Water Reactions

Practically insoluble in water (17mg/L). Hydrolyzed by strong acid.

Reactivity Profile

DIPHACINONE is a ketone, and behaves as a weak acid. Forms water soluble alkali metal salts. Ketones are reactive with many acids and bases liberating heat and flammable gases (e.g., H2). The amount of heat may be sufficient to start a fire in the unreacted portion of the ketone. Ketones react with reducing agents such as hydrides, alkali metals, and nitrides to produce flammable gas (H2) and heat. Ketones are incompatible with isocyanates, aldehydes, cyanides, peroxides, and anhydrides. They react violently with aldehydes, HNO3, HNO3 + H2O2, and HClO4.

Health Hazard

DIPHACINONE is extremely toxic; probable oral lethal dose in humans is 5-50 mg/kg, or between 7 drops and 1 teaspoonful for a 150-lb. person. Many medical conditions will be aggravated by DIPHACINONE.

Fire Hazard

When heated to decomposition DIPHACINONE emits acrid smoke and fumes. Sensitive to light.

Agricultural Uses

Rodenticide: A U.S. EPA restricted Use Pesticide (RUP) when the formulation contains 3% or more of diphacinone. Diphacinone is an anti-coagulant rodenticide bait used for control of rats, mice, voles and other rodents. It is available in meal, pellet, wax block, and liquid bait formulations, as well as in tracking powder and concentrate formulations. It is used in general agriculture and in food-processing areas. The top five uses for diphacinone in California are on landscapes, general vertebrate pest control, around structures and right of ways, and on oranges. This material is also used as an anticoagulant medication. Not approved for use in EU countries.

Trade name

DE-PESTER®[C]; DIDANDIN®; DIPAXIN®; DITRAC®; GOLD CREST®; KILL-RO RAT KILLER®; LIQUA-TOX®, diphacinone sodium salt; ORAGULANT®; P. C. Q. ®; PID®; PROMAR®; RAMIK®; RAT KILLER®; RODENT CAKE®[C]; SOLVAN®; TOMCAT®; U 1363®

Safety Profile

Poison by ingestion. Inlxbits blood clotting, leading to hemorrhages. Action similar to coumadin (warfarin). A pesticide used in rodent control. When heated to decomposition it emits acrid smoke and irritating fumes

Metabolic pathway

Diphacinone is a member of the indandione class of anti-coagulants. Its fate in rats and mice has been reported but no information on its degradation in soil or plants has been published. It is metabolised by hydroxylation and conjugation.

2-(diphenylacetyl)-1h-indene-1,3(2h)-dione 2-(diphenylacetyl)-1h-indene-2,3(2h)dione 2-(Diphenylacetyl)indan-1,3-dione 2-Diphenylacetyl-1,3-indandione ide A 2-diphenylacetyl-1,3-indanedione 2-diphenylacetyl-3-indandione 2-Diphenyl-acetyl-indan-1,3-dion 3(2H)-dione,2-(diphenylacetyl)-1H-Indene-1 contrax-d Didion Dipaxin Diphac diphacin(turkey) 2-(DIPHENYLACETYL)-1,3-DIKETOHYDRINDENE 2-DIPHENYLACETYL-1,3-INDANDIONE 2-(2,2-DIPHENYLACETYL)INDAN-1,3-DIONE DIPHACINONE, 100MG, NEAT diphacinone (ansi,bsi,iso) 2-(DIPHENYLACETYL)INDENE-1,3-DIONE DID AND IN DIPHACIN DIPHACINONE DIPHENADIONE 1,3-Indandione, 2-(diphenylacetyl)- 1H-Indene-1,3(2H)-dione, 2-(diphenylacetyl)- 2-(2,2-Diphenylacetyl)-1,3-indandione 2-(Diphenylacetyl)-1H-indene-1,3-(2H)-dione diphacinon(presentinfreeformorassodiumsalt) diphacins Diphenacin Diphenadion Diphenandione Diphenylacetylindandione goldcrest Kill-ko rat killer kill-koratkiller Oragulant p.c.q. parakakes pcq Promar promarpcq Ramik Ratindan Ratindan 1 ratindan1 rodentcake Solvan u 1363 u1363 u-1363 URI 788 diphacinone (ISO) 2-diphenylacetylindan-1,3-dione 2-(diphenylacetyl)-1,3-indene dione Diphacin 10 Diphenadione Ramik Yasodion 2-(2,2-Diphenylacetyl)-1H-indene-1,3(2H)-dione