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SULFALLATE

CAS No.
95-06-7
Chemical Name:
SULFALLATE
Synonyms
CDEC;cp4572;cp4742;Vegedex;CDEC(R);CP 4572;cp4,742;Vegadex;CP 4,742;NSC 16085
CBNumber:
CB8270999
Molecular Formula:
C8H14ClNS2
Molecular Weight:
223.79
MDL Number:
MFCD00048530
MOL File:
95-06-7.mol
Last updated:2023-05-04 17:34:44

SULFALLATE Properties

Melting point 25°C
Boiling point bp1 128-130°
Density d25 1.088
refractive index nD25 1.5822
Flash point >100 °C
storage temp. APPROX 4°C
pka 0.71±0.50(Predicted)
Water Solubility 0.1g/L(25 ºC)
Merck 13,8996
Stability Stable. Incompatible with alkalies, strong oxidizing agents.
EWG's Food Scores 3
FDA UNII 7U7BI7173J
Proposition 65 List Sulfallate
IARC 2B (Vol. 30, Sup 7) 1987
EPA Substance Registry System Sulfallate (95-06-7)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS08,GHS07,GHS09
Signal word  Danger
Hazard statements  H302-H350-H410
Precautionary statements  P264-P270-P301+P312-P330-P501-P273-P391-P501
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
Toxicity LD50 orally in rats: 850 mg/kg (Bailey, White)

SULFALLATE price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Medical Isotopes, Inc. 42262 Sulfallate 95-06-7 100mg $650 2021-12-16 Buy
American Custom Chemicals Corporation PST0000297 SULFALLATE 95.00% 95-06-7 100MG $750.75 2021-12-16 Buy
American Custom Chemicals Corporation PST0000297 SULFALLATE 95.00% 95-06-7 1G $1963.5 2021-12-16 Buy
Medical Isotopes, Inc. 42262 Sulfallate 95-06-7 1g $2200 2021-12-16 Buy
Product number Packaging Price Buy
42262 100mg $650 Buy
PST0000297 100MG $750.75 Buy
PST0000297 1G $1963.5 Buy
42262 1g $2200 Buy

SULFALLATE Chemical Properties,Uses,Production

Chemical Properties

Sulfallate is an amber liquid.

Uses

Sulfallate is a selective pre-planting or pre-emergence herbicide.

Definition

ChEBI: Sulfallate is a thiocarbonyl compound.

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.

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.

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

Carcinogenicity

Sulfallate is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals.

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.

SULFALLATE Preparation Products And Raw materials

Raw materials

Preparation Products

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2-chloro-2-propenyldiethylcarbamodithioate 2-Chloroallyl N,N-diethyldithiocarbamate 2-chloroallyln,n-diethyldithiocarbamate 2-Propene-1-thiol, 2-chloro-, diethyldithiocarbamate Carbamic acid, diethyldithio-, 2-chloroallyl ester Carbamodithioic acid, diethyl-, 2-chloro-2-propenyl ester Chlorallyl diethyldithiocarbamate vegadexsuper Vegedex 2-Chlorallyl diethyldithiocarbamate 2-CHLORALLYL-ESTER 2-CHLOROALLYL DIETHYLDITHIOCARBAMATE DIETHYLDITHIOCARBOMIC ACID 2-CHLOROALLYL ESTER DIETHYLDITHIOCARBAMIC ACID, 2-CHLORALLYL ESTER DIETHYLDITHIOCARBAMIC ACID 2-CHLOROALLYL ESTER CP 4742(R) CDEC CDEC(R) SULFALLATE VEGADEX(R) SULFALLATE PESTANAL (S-2-CHLORALLYL- N,N-DIETHYLDITHIOCARBAMATE) cdec (wssa) sulfallate (bsi,iso) SULPHALLATE sulfallate (ISO) 2-chloroallyl N,N-dimethyldithiocarbamate N,N-Diethyldithiocarbamic acid 2-chloroallyl SULFALLATE, 2-chloroallyl N,N-dimethyldithiocarbamate 2-chloroprop-2-enyl N,N-diethylcarbamodithioate N,N-diethylcarbamodithioic acid 2-chloroallyl ester N,N-DiethylcarbaModithioic Acid 2-Chloro-2-propen-1-yl Ester NSC 16085 chlorallyldiethyldithiocarbamate CP 4,742 CP 4572 cp4,742 cp4572 cp4742 Diethylcarbamodithioic acid 2-chloro-2-propenyl ester diethyl-carbamodithioicaci2-chloro-2-propenylester diethylcarbamodithioicacid2-chloro-2-propenylester diethyldithio-carbamicaci2-chloroallylester NCI-C00453 Thioallate Vegadex Vegadex super 2-chloro-2-propene-1-thiodiethyldithiocarbamate 2-Chloro-2-propene-1-thiol diethyldithiocarbamate 2-chloro-2-propene-1-thioldiethyldithiocarbamate 2-Chloro-2-propenyl diethylcarbamodithioate 2-Chloro-2-propenyl diethyldithiocarbamate XJCLWVXTCRQIDI-UHFFFAOYSA-N Carbamodithioic acid, N,N-diethyl-, 2-chloro-2-propen-1-yl ester 95-06-7 34-85-7 199-56-7 1995/6/7 1995-06-7 C8H14ClNS2