DESIGNATIONS
CAS No.: 72-20-8
Registry name: Endrin
Chemical name: 1,2,3,4,10,10-Hexachloro-6,7-epoxy-1,4,4a,5,7,8,8a-octahydro-1,4-endo,endo-5,8-dimethanonaphthalene
Synonyms, Trade names: Hexadrin, Mendrin, Compound 269
Chemical name (German): Endrin, 1,2,3,4,10,10-Hexachlor-6,7-epoxy-1,4,4a,5,7,8,8a-octahydro-1,4-endo,endo-5,8-dimethanonaphthalin
Chemical name (French): Endrine; 1,2,3,4,10,10-hexachloro-6,7-époxy-1,4,4a,5,6,7,8,8a-octahydro-1,4-endo,endo-5,8-diméthanonaphtaléne
Appearance: colourless crystalline powder (technical product with 92 % endrin brownish-yellow); commercially available products are dissolved in organic solvents
BASIC CHEMICAL AND PHYSICAL DATA
Empirical formula: |
C12H8Cl6O |
Rel. molecular mass: |
380.93 g |
Density: |
1.77 g/cm3 (technical product) |
Melting point: |
> 200°C (decomposition) |
Vapour pressure: |
2.6 x 10-5 Pa |
Explosion limits: |
1.1-7 % by vol. in air (technical product) |
Solvolysis/solubility: |
in water: virtually insoluble (0.23 mg/l) soluble in acetone, benzene, ethanol, aromatic hydrocarbons, esters and ketones |
Conversion factors: |
1 ppm = 15.8 mg/m3 1 mg/m3 = 0.06 ppm |
ORIGIN AND USE
Usage:
Used as a non-systemic insecticide, acaricide and rodenticide for grain.
Origin/derivation:
Endrin is produced as a side product of hexachlorocyclopentadiene and vinyl chloride with
cyclopentadiene. Endrin also forms when isodrin is epoxidised with peracetic acid and
perbenzoic acid. The degradation of dieldrin in the environment produces endrin (refer
also to 'dieldrin' information sheet).
Toxicity
Mammals: |
||
Rat: |
LD50 7-43 mg/kg, oral |
acc. MERCIER, 1981 |
LD50 15 mg/kg, dermal |
acc. UBA, 1986 |
|
Mouse: |
LD50 1,370 µg/kg, oral |
acc. UBA, 1986 |
LD50 2,300 µg/kg, intravenous |
acc. UBA, 1986 |
|
TDLo 11 mg/kg, oral, 7.-17. d of pregnancy |
acc. UBA, 1986 |
|
Monkey: |
LD50 3 mg/kg, oral |
acc. MERCIER, 1981 |
Rabbit: |
LD50 60 mg/kg, dermal |
acc. UBA, 1986 |
Guinea pig: |
LD50 16 mg/kg, oral |
acc. UBA, 1986 |
Pig: |
LD50 5,600 µg/kg, oral |
acc. UBA, 1986 |
LD50 1,500 µg/kg, intravenous |
acc. UBA, 1986 |
|
Aquatic organisms: |
||
Carp: |
TL 0.005 ppm (48h) |
acc. UBA, 1986 |
Fish: |
0.013-0.004 mg/l |
acc. UBA, 1986 |
Organisms on which fish feed: |
0.1 mg/l |
acc. UBA, 1986 |
Characteristic effects:
Humans/mammals: As a central spasmodic agent, endrin is highly toxic in humans. Skin resorption is possible. Characteristic symptoms are already encountered following the intake of 1 mg/kg (UBA, 1986). 5 - 50 mg/kg are toxic and more than 6 g are lethal (MERCIER, 1981). Excretion via the kidneys and intestines is very slow (risk of accumulation). There is also damage to the liver, kidneys and central nervous system. Chlorine dioxide poisoning is often encountered due to metabolisation in the body.
ENVIRONMENTAL BEHAVIOUR
Water:
Endrin is virtually insoluble in water and sinks to the bottom. However, its
commercial products mix or disperse in water to form toxic, milky 'broths'. Endrin is also
sensitive to strong acids. It therefore has a highly toxic effect particularly on fish and
the organisms on which they feed and may harm all types of water. In Germany it is listed
in class 3 of the catalogue of substances hazardous to water (highly hazardous).
(Refer also to 'dieldrin')
ENVIRONMENTAL STANDARDS
Medium/ acceptor |
Sector |
Country/ organ. |
Status |
Value |
Cat. |
Remarks |
Source |
Water: | Drinkw | USA | L | 0.0002 mg/l | MCL | Long-time value | acc. SCHROEDER, 1985 |
Drinkw | USA | G | 0.0005 mg/l | In State of Illinois | acc. WAITE, 1984 | ||
Waste water | EC | L | 5 mg/l | Seawater | acc. LEROY, 1985 | ||
Waste water | EC | L | 5 mg/l | Freshwater | acc. LEROY, 1985 | ||
Air: | Workp | D | L | 0.1 mg/m3 | MAK | DFG, 1989 | |
Workp | USA | (L) | 0.1 mg/m3 | TWA | ACGIH, 1986 | ||
Foodstuffs: | 0.2 ng/kg/d | ADI | acc. MERCIER, 1981 |
Note:
There has been a complete ban on the use of endrin in the Federal Republic of Germany
since 1988.
Comparison/reference values
(Refer to 'dieldrin')
Assessment/comments
(Refer to 'dieldrin')