| Identification | Back Directory | [Name]
SULFALLATE | [CAS]
95-06-7 | [Synonyms]
CDEC
cp4572
cp4742
Vegadex
Vegedex
CP 4572
cp4,742
CDEC(R)
CP 4,742
NSC 16085
CP 4742(R)
SULFALLATE
VEGADEX(R)
NCI-C00453
Thioallate
cdec (wssa)
SULPHALLATE
vegadexsuper
Vegadex super
2-CHLORALLYL-ESTER
sulfallate (bsi,iso)
chlorallyldiethyldithiocarbamate
Chlorallyl diethyldithiocarbamate
2-Chlorallyl diethyldithiocarbamate
2-CHLOROALLYL DIETHYLDITHIOCARBAMATE
2-chloroallyln,n-diethyldithiocarbamate
2-Chloroallyl N,N-diethyldithiocarbamate
2-Chloro-2-propenyl diethyldithiocarbamate
2-chloro-2-propenyldiethylcarbamodithioate
2-Chloro-2-propenyl diethylcarbamodithioate
diethyldithio-carbamicaci2-chloroallylester
N,N-Diethyldithiocarbamic acid 2-chloroallyl
DIETHYLDITHIOCARBOMIC ACID 2-CHLOROALLYL ESTER
DIETHYLDITHIOCARBAMIC ACID, 2-CHLORALLYL ESTER
DIETHYLDITHIOCARBAMIC ACID 2-CHLOROALLYL ESTER
2-chloro-2-propene-1-thiodiethyldithiocarbamate
2-chloroprop-2-enyl N,N-diethylcarbamodithioate
2-chloro-2-propene-1-thioldiethyldithiocarbamate
2-Chloro-2-propene-1-thiol diethyldithiocarbamate
Carbamic acid, diethyldithio-, 2-chloroallyl ester
diethyl-carbamodithioicaci2-chloro-2-propenylester
diethylcarbamodithioicacid2-chloro-2-propenylester
N,N-diethylcarbamodithioic acid 2-chloroallyl ester
2-Propene-1-thiol, 2-chloro-, diethyldithiocarbamate
Diethylcarbamodithioic acid 2-chloro-2-propenyl ester
SULFALLATE, 2-chloroallyl N,N-dimethyldithiocarbamate
Carbamodithioic acid, diethyl-, 2-chloro-2-propenyl ester
sulfallate (ISO) 2-chloroallyl N,N-dimethyldithiocarbamate
N,N-DiethylcarbaModithioic Acid 2-Chloro-2-propen-1-yl Ester
SULFALLATE PESTANAL (S-2-CHLORALLYL- N,N-DIETHYLDITHIOCARBAMATE) | [EINECS(EC#)]
205-701-7 | [Molecular Formula]
C8H14ClNS2 | [MDL Number]
MFCD00048530 | [MOL File]
95-06-7.mol | [Molecular Weight]
223.79 |
| Chemical Properties | Back Directory | [Appearance]
amber liquid | [Melting point ]
25°C | [Boiling point ]
bp1 128-130° | [density ]
d25 1.088 | [refractive index ]
nD25 1.5822 | [Fp ]
>100 °C | [storage temp. ]
APPROX 4°C
| [pka]
0.71±0.50(Predicted) | [Stability:]
Stable. Incompatible with alkalies, strong oxidizing agents. | [Water Solubility ]
0.1g/L(25 ºC) | [Merck ]
13,8996 | [IARC]
2B (Vol. 30, Sup 7) 1987 | [EPA Substance Registry System]
Sulfallate (95-06-7) |
| Hazard Information | Back Directory | [Chemical Properties]
amber liquid | [Uses]
Sulfallate is a selective pre-planting or pre-emergence herbicide. | [Uses]
Herbicide. | [General Description]
Amber to dark amber liquid. | [Air & Water Reactions]
Insoluble in water. Thio and dithiocarbamates slowly decompose in aqueous solution to form carbon disulfide and methylamine or other amines. Such decompositions are accelerated by acids. | [Reactivity Profile]
SULFALLATE is incompatible with strong oxidizing agents .Also incompatible with alkalis. . | [Fire Hazard]
SULFALLATE is probably combustible. | [Potential Exposure]
A dithiocarbamate. The major use for sulfallate in the United States is as a preemergent selective herbicide to control certain annual grasses and broadleaf weeds around vegetable and fruit crops. Sulfallate has also been used for weed control among shrubbery and ornamental plants. Some dithiocarbamates have been used as rubber components | [First aid]
Skin Contact: Flood all areas of body that have contacted the substance with water. Don’t wait to remove contaminated clothing; do it under the water stream. Use soap to help assure removal. Isolate contaminated clothing when removed to prevent contact by others. Eye Contact: Remove any contact lenses at once. Flush eyes well with copious quantities of water or normal saline for at least 2030 minutes. Seek medical attention. Inhalation: Leave contaminated area immediately; breathe fresh air. Proper respiratory protection must be supplied to any rescuers. If coughing, difficult breathing or any other symptoms develop, seek medical attention at once, even if symptoms develop many hours after exposure. Ingestion: If convulsions are not present, give a glass or two of water or milk to dilute the substance. Assure that the person’s airway is unobstructed and contact a hospital or poison center immediately for advice on whether or not to induce vomiting. | [Shipping]
UN2771 Dithiocarbamate and Thiocarbamate pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials. UN3082 Environmentally hazardous substances, liquid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required. | [Incompatibilities]
Dithiocarbamate esters are combustible. They react violently with powerful oxidizers such as calcium hypochlorite. Poisonous gases are generated by the thermal decomposition of dithiocarbamate compounds, including carbon disulfide, oxides of sulfur, oxides of nitrogen, hydrogen sulfide, ammonia, and methylamine.Thio and dithiocarbamates slowly decompose in aqueous solution to form carbon disulfide and methylamine or other amines. Such decompositions are accelerated by acids. Flammable gases are generated by the combination of dithiocarbamate with aldehydes, nitrides, and hydrides. Dithiocarbamate are incompatible with acids, peroxides, and acid halides. | [Waste Disposal]
Small amounts may be decomposed by strong oxidizing agent. Large amounts should be incinerated in a unit with effluent gas scrubbing. | [Definition]
ChEBI: Sulfallate is a thiocarbonyl compound. | [Carcinogenicity]
Sulfallate is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals. |
| Safety Data | Back Directory | [Hazard Codes ]
T,N | [Risk Statements ]
45-22-50/53 | [Safety Statements ]
53-45-60-61 | [RIDADR ]
UN3082 9/PG 3 | [RTECS ]
EZ5075000 | [HS Code ]
29302000 | [Safety Profile]
Confirmed carcinogen
with experimental carcinogenic data.
Moderately toxic by ingestion and skin
contact. Mutation data reported. An
herbicide. When heated to decomposition it
emits very toxic fumes of Cl-, NOx, and
SOx. See also ALLYL COMPOUNDS,
CARBAMATES, and ESTERS. | [Hazardous Substances Data]
95-06-7(Hazardous Substances Data) | [Toxicity]
LD50 orally in rats: 850 mg/kg (Bailey, White) |
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