Testing Information

Testing Status of Agents at NTP

CAS Registry Number: 8001-35-2

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http://ntp.niehs.nih.gov/go/22435

Selected information from two of the National Library of Medicine's databases: ChemIDPlus1 and HSDB2.

Names (NTP)

  • Toxaphene
  • CAMPHECHLOR

Structure

Chemical Structure for CAS Registry Number 8001-35-2 from NLM

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Chemical Properties2

Property Description
Color/Form
  • Yellow waxy solid.
  • Amber, waxy solid.
Odor
  • Pleasant piney odor
  • Mild odor of chlorine and camphor
  • Mild, turpentine-like odor
  • Mild, piney, chlorine- and camphor-like odor.
Taste
  • None found
Boiling Point
  • Decomposes
Melting Point
  • 65-90 deg C
Molecular Weight
  • 414 (avg)
Corrosivity
  • Noncorrosive in the absence of moisture
  • Corrosive to iron
  • Solution in xylene may produce corrosive products when heated.
Critical Temperature & Pressure
  • None found
Density/Specific Gravity
  • 1.65 @ 25 deg C
Disassociation Constants
  • None found
Heat of Combustion
  • None found
Heat of Vaporization
  • None found
log P (octanol-water)
  • The median log Kow for toxaphene is 5.90.
pH
  • None found
Solubilities
  • Freely sol in aromatic hydrocarbons
  • READILY SOL IN ORG SOLVENTS INCL PETROLEUM OILS
  • 3 mg/l water @ room temp
  • > 450 g/100 ml benzene
  • > 450 g/100 ml carbon tetrachloride
  • > 450 g/100 ml ethylene dichloride
  • > 450 g/100 ml xylene
  • 280 g/100 ml kerosene
  • 55-60 g/100 ml mineral oil
  • More soluble in aromatic than aliphatic hydrocarbons.
  • In water, 0.55 mg/l @ 20 deg C
Spectral Properties
  • Toxaphene has a maximum absorbance at 260 nm in hexane. IR showed a strong band at 1280-1308/cm. **PEER REVIEWED**
Surface Tension
  • None found
Vapor Density
  • 14.3 (air= 1)
Vapor Pressure
  • 6.69X10-6 mm Hg @ 20 deg C
Relative Evaporation Rate
  • None found
Viscosity
  • None found
Other Properties
  • DEHYDROCHLORINATED BY CERTAIN CATALYSTS SUCH AS IRON
  • Decomposes near boiling point
  • Clear, amber-colored, and viscous liquid, mild terpene odor, specific gravity: 1.519-1.567 at 25 deg C/25 deg C; readily sol in most commercial organic solvents and is more sol in aromatic than in aliphatic hydrocarbons /Strobane T-90/
  • The commercial product is relatively stable but may be degraded by losing hydrogen chloride or chlorine upon prolonged exposure to sunlight, alkali, or high temperatures above 120 deg C. Toxaphene and its components may be dechlorinated by reaction with tin hydrides.
  • Henry's Law constant= 6.00X10-6 atm cu m/ mole @ 20 deg C

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Uses2

  • For Toxaphene (USEPA/OPP PC Code: 080501) there are 0 labels match. /SRP: Not registered for current use in the U.S./
  • /SRP:/ Approved uses of pesticides are established by the US EPA and may change periodically. Local and state authorities should be consulted for currently approved uses. The following web site also addresses current uses of pesticides approved by the US EPA and by the state of California: . **PEER REVIEWED**
  • The active ingredient is no longer contained in any registered pesticide products ... "cancelled."
  • IT IS A NON-SYSTEMIC CONTACT AND STOMACH INSECTICIDE WITH SOME ACARICIDAL ACTION
  • INSECTICIDE FOR COTTON, PEAS, SOYBEANS, PEANUT, CORN, WHEAT & OTHER SMALL GRAINS, EG, RICE (FORMER USE), ALFALFA, SORGHUM (FORMER USE), CATTLE, SHEEP, GOATS, SWINE, & HORSES (FORMER USE), FRUITS & NUTS (FORMER USE), ORNAMENTALS, FORAGE, & TURF (FORMER USE), & CERTAIN AGRICULTURAL PREMISES (FORMER USE) **PEER REVIEWED**
  • As dip to control scabies on cattle & sheep; minor use: for armyworms, cutworms, & grasshoppers; for mealybug & pineapple gummosis moth control on pineapples & weevil control on bananas
  • CONTROL OF CASSIA OBTUSIFOLIA IN SOYBEANS; USED FOR CONTROL OF ANIMAL ECTOPARASITES
  • Conditional and restricted use as an insecticide and as a miticide in foliar treatment of: cranberries, strawberries, apples, pears, quinces, nectarines, peaches, bananas, pineapple, eggplant, peppers, pimentos, tomatoes, broccoli, brussel sprouts, cabbage, cauliflower, collards, kale, kohlrabi, spinach, lettuce (head and leaf), parsnips, rutabagas, beans (lima, green and snap), corn (sweet), cowpeas, okra, alfalfa, barley, oats, rice, rye, wheat, celery, cotton, horseradish, peanuts, peas, sunflowers, soybeans, ornamental plants, birch, elm, hickory, maple oak, and noncrop areas. Also used in seed crop foliar treatment of clover and trefoil; in soil treatment of corn; in back rubber of beef cattle; in animal treatment of goats, sheep, beef cattle, and hogs; and aerial application and tank mixtures. /Toxaphene 8 Emulsifiable Insecticide/
  • Conditional and restricted use as an insecticide and as a miticide in foliar treatment of small grains, corn, and cotton. Also used in aerial application. /Rigo toxaphene 8, For use only under special emergency exemptions/
  • Restricted use as an insecticide and as a miticide in foliar treatment of barley, oats, rice, wheat, cotton, and soybeans and in aerial application.
  • Unclassified use as an insecticide and as a miticide in manufacturing only.
  • Conditional and unclassified uses as an insecticide and as a miticide in foliar treatment of cranberries, strawberries, grapefruit, kumquat, lemons, limes, oranges, tangelos, tangerines, apples, pears, eggplant, tomatoes, broccoli, brussel sprouts, cabbage, cauliflower, lettuce, spinach, carrots, onions, parsnips, rutabagas, beans (dry, lima, green), barley, rice, rye, celery, corn, cotton, soybeans, wheat, oak, and alfalfa (seed crop). Also used in aerial application.
  • Conditional and restricted use as an insecticide and as a miticide in foliar treatment of bananas and pineapple; in animal treatment of sheep and beef cattle; and in aerial application.
  • Used as an insecticide and as a miticide in foliar treatment of peanuts, soybeans, and cotton; also, used in aerial application and tank mixtures. /Hercules Toxaphene 72% Emulsifiable Concentrate/
  • Used as an insecticide and as a miticide in foliar treartment of barley, oats, sunflowers, and wheat; also, used in aerial application. /Red Top Toxaphene 8 Spray/
  • The largest single use of toxaphene is as a pesticide on cotton crops. Other major uses are on cattle and swine ... and other food crops.

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Superlist Classes1

  • ATSDR Profile Priority List, rank : 30
  • Overall Carcinogenic Evaluation: Group 2B
  • Reasonably anticipated to be a carcinogen
  • Reportable Quantity (RQ) = 1 lb
  • Threshold Planning Quantity (TPQ) = 500/10000 lb
  • TWA 0.5 mg/m3; STEL 1 mg/m3; skin; Confirmed animal carcinogen with unknown relevance to humans
  • TWA 0.5 mg/m3; skin

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Notes (Sources: NTP,HSDB,RTECS,MESH)1

  • None found

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Other Registry Numbers1

  • 8022-04-6

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Synonyms (Sources: NTP, HSDB,RTECS,MESH)1

  • M 5055
  • Agricide Maggot Killer
  • Agricide maggot killer (F)
  • Agro-Chem Brand Torbidan 28
  • Agro-Chem Brand Toxaphene 6E
  • Agsco toxaphene
  • Agway toxaphene 6E
  • Alltex
  • Alltox
  • Anatox
  • Attac 4-2
  • Attac 4-4
  • Attac 6
  • Attac 6-3
  • Attac 8
  • Camphechlor
  • Camphochlor
  • Camphofene huileux
  • Chem-Phene
  • Chlorinated camphene
  • Chlorocamphene
  • Clor Chem T-590
  • Compound 3956
  • Cotton-Tox MP 82
  • Crestoxo
  • Cristoxo 90
  • Dr Roger's TOX-ENE
  • ENT 9,735
  • Estonox
  • Fasco-terpene
  • Felco/Land O'Lakes Toxaphene
  • Geniphene
  • Grower Service Toxaphene 6E
  • Grower Service Toxaphene MP
  • Gy-phene
  • Hercules 3956
  • Hercules Toxaphene Emulsifiable Concentrate
  • HSDB 1616
  • Kamfochlor
  • Melipax
  • Motox
  • NCI-C00259
  • Octachlorocamphene
  • PchK
  • Penphene
  • Phenacide
  • Phenatox
  • Polychlorocamphene
  • RCRA waste number P123
  • Red Top Toxaphene 8 Spray
  • Rigo Toxaphene 8
  • Royal Brand Bean Tox 82
  • Security Motox 63 cotton spray
  • Security Tox-MP cotton spray
  • Security Tox-Sol-6
  • Strobane-T
  • Strobane T-90
  • Synthetic 3956
  • Toxadust
  • Toxakil
  • Toxaphen
  • Toxaphene E-8
  • Toxaphene 90-10
  • Toxaphene 8 EC
  • Toxaphene 8 Emulsifiable Insecticide
  • Toxon 63
  • Toxyphen
  • Vertac 90%
  • Vertac toxaphene 90

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Links to Additional Information1

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Footnotes

1 Source: the National Library of Medicine's ChemIDPlus, 10/28/2007.

2 Source: the National Library of Medicine's Hazardous Substance Database, 10/28/2007.