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DIALLATE

DIALLATE Structure
CAS No.
2303-16-4
Chemical Name:
DIALLATE
Synonyms
DATC;Avadex;cp15336;Diallat;Pyradex;2,3-DCDT;Avadex I;DIALLATE;CP 15336;cp15,336
CBNumber:
CB3751152
Molecular Formula:
C10H17Cl2NOS
Molecular Weight:
270.22
MOL File:
2303-16-4.mol
MSDS File:
SDS
Modify Date:
2024/7/2 8:55:06

DIALLATE Properties

Melting point 25-30℃
Boiling point bp9 150°
Density 1.1556 (rough estimate)
refractive index 1.6000 (estimate)
Flash point >100 °C
storage temp. 0-6°C
form Viscous Liquid
pka -1.63±0.70(Predicted)
color Colorless to light yellow
Water Solubility 40mg/L(room temperature)
IARC 3 (Vol. 30, Sup 7) 1987
EPA Substance Registry System Diallate (2303-16-4)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS08,GHS07,GHS09
Signal word  Warning
Hazard statements  H302-H351-H410
Precautionary statements  P264-P270-P301+P312-P330-P501-P201-P202-P281-P308+P313-P405-P501-P273-P391-P501
Hazard Codes  Xn,N
Risk Statements  22-40-50/53
Safety Statements  25-36/37-60-61
RIDADR  2902
RTECS  EZ8225000
HazardClass  6.1(b)
PackingGroup  III
HS Code  29302000
Toxicity LD50 orally in rats: 395 mg/kg (Bailey, White)

DIALLATE Chemical Properties,Uses,Production

Chemical Properties

Diallate is a brown liquid.

Uses

Diallate is a pesticide used to treat fruits and vegetables. Environmental wastewater pollutant.Environmental toxin on US EPA Toxic Release Inventory list (TRI) list.

General Description

Used as an herbicide.

Air & Water Reactions

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

DIALLATE is a thiocarbamate ester. Flammable gases are generated by the combination of thiocarbamates and dithiocarbamates with aldehydes, nitrides, and hydrides. Thiocarbamates and dithiocarbamates are incompatible with acids, peroxides, and acid halides.

Safety Profile

Poison by ingestion. Moderately toxic by skin contact. Questionable carcinogen with experimental carcinogenic and tumorigenic data. Mutation data reported. When heated to decomposition it emits very toxic fumes of Cl-, NOx, and SOx. See also CARBAMATES and ALLYL COMPOUNDS.

Potential Exposure

A thiocarbamate herbicide. The slow release of poisonous gases from hydrolysis of many thio and dithiocarbamates requires the use of respirators during handling. Poisoning can also occur by ingestion and absorption through the skin. Diallate is potential danger to those involved in the manufacture, formulation and applica- tion of this re-emergence herbicide.

Environmental Fate

Soil. Soil metabolites include 2,3-dichloroallyl alcohol, 2,3-dichloroallyl mercaptan (Hartley and Kidd, 1987) and carbon dioxide (Smith, 1988). The formation of the alcohol occurs via hydrolysis of the ester linkage and transthiolation of the allylic group (Kaufman, 1967). In an agricultural soil, 14CO2 was the only biodegradation identified; however, bound residue and traces of benzene and water-soluble radioactivity were also detected in large amounts (Anderson and Domsch, 1980). The reported half-lives in soil range from 2 to 4 weeks to (Smith and Fitzpatrick, 1970) to approximately 30 days (Hartley and Kidd, 1987). Diallate did not migrate deeper than 5 cm on test field plots (Smith, 1970). In four microbially-active agricultural soils, the half-life was 4 weeks but in sterilized soil the half-life was 20 weeks (Anderson and Domsch, 1976).
Plant. In plants, diallate is metabolized and carbon dioxide is released (Hartley and Kidd, 1987). Diallate undergoes cis/trans isomerization and oxidative cleavage when irradiated at 300 nm forming 2,3-dichloroacrolein and 2-chloroacrolein as products (Ruzo and Casida, 1985).
Photolytic. Irradiation of diallate was also conducted in oxygenated chloroform or water until a 10% conversion was obtained. Products formed included acetaldehyde, 2,3- dichloroacrolein and trace amounts of 2-chloroacrolein (Ruzo and Casida, 1985). Chemical/Physical. Emits toxic fumes of chlorine, nitrogen and sulfur oxides when heated to decomposition (Sax and Lewis, 1987). Though no products were reported, the calculated hydrolysis half-life at 25°C and pH 7 is 6.6 years (Ellington et al., 1988).

Shipping

UN2992 Carbamate pesticides, liquid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials.

Incompatibilities

hiocarbamate esters are combustible. They react violently with powerful oxidizers such as calcium hypochlorite. Poisonous gases are generated by the thermal decomposition of thiocarbamate compounds, including carbon disulfide, oxides of sulfur, oxides of nitro- gen, hydrogen sulfide, ammonia, and methylamine. Many materials in this group slowly decompose in aqueous solu- tion to form carbon disulfide and methylamine or other amines. Such decompositions are accelerated by acids. Flammable gases are generated by the combination of thiocarbamates with aldehydes, nitrides, and hydrides. Thiocarbamates are incompatible with acids, peroxides, and acid halides.

Waste Disposal

Land burial is acceptable for small quantities. Larger quantities can be incinerated . In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers. Must be disposed properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal.

DIALLATE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 71)Suppliers
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Hubei yongkuo Technology Co., Ltd 027-59223108 15972152991 China 9993 58 Inquiry
S-2,3-DICHLOROALLYL DIISOPROPYL THIOCARBAMATE S-[2,3-DICHLOROALLYL]-N,N'-DI-ISOPROPYL THIOCARBAMATE DIALLATE MIXTURE OF CIS AND TRANS ISOME& DIALLATE, 100MG, NEAT 2,3-DCDT 2,3-dichlorallyl-n,n-(diisopropyl)-thiocarbamat 2,3-Dichlorallyl-N,N-(diisopropyl)-thiocarbamate 2,3-dichloro-2-propene-1-thiodiisopropylcarbamate 2,3-Dichloro-2-propene-1-thiol, diisopropylcarbamate 2,3-dichloro-2-propene-1-thiol,diisopropylcarbamate 2-Propene-1-thiol, 2,3-dichloro-, diisopropylcarbamate Avadex Avadex I Avadex II Bis(1-methylethyl) carbamothioic acid, S-(2,3-dichloro-2-propenyl)ester bis(1-methylethyl)carbamothioicacid,s-(2,3-dichloro-2-propenyl)ester di-allate (bsi,e-iso) diallate (f-iso,wssa) Diallate (95-98%) SEC-2,3-DICHLOROALLYLDIISOPROPYLTHIOCARBAMATE Diallate(cisortrans) di-allate (ISO) S-(2,3-dichloroallyl)-N,N-diisopropylthiocarbamate Di-allate 100mg [2303-16-4] Diallate Standard S-[(2Z)-2,3-Dichloro-2-propenyl] diisopropylthiocarbamate AVADEX(R) DIALLATE DATC 2,3-Dichloroallyl-N,N-diisopropylthiolcarbamate Carbamic acid, diisopropylthio-, S-(2,3-dichloroallyl) ester carbamicacid,diisopropylthio-,s-(2,3-dichloroallyl)ester Carbamothioicacid,bis(1-methylethyl)-,S-(2,3-dichloro-2-propenyl)ester CP 15,336 CP 15336 cp15,336 cp15336 Diallaat Diallat Dichloroallyl diisopropylthiocarbamate dichloroallyldiisopropylthiocarbamate Diisopropylthiocarbamic acid, S-(2,3-dichloroallyl) ester diisopropylthiocarbamicacid,s-(2,3-dichloroallyl)ester DiisopropylthiocarbamicacidS-2,3-dichloroallylester Di-isopropylthiolocarbamate de S-(2,3-dichloro allyle) di-isopropylthiolocarbamatedes-(2,3-dichloroallyle) di-isopropylthiolocarbamatedes-(2,3-dichloroallyle)(french) Pyradex Rcra waste number U062 rcrawastenumberu062 S-(2,3-Dichlor-allyl)-N,N-diisopropyl-monothiocarbamaat s-(2,3-dichloro-2-propenyl)bis(1-methylethyl)carbamothioate S-(2,3-Dichloro-allil)-N,N-diisopropil-monotiocarbammato S-(2,3-dichloroallyl) diisopropylcarbamothioate Diallate(Mixture of E and Z isomer) Diallate @100 μg/mL in MeOH Di-allateSolution,1000mg/L,1ml Diallate (95-98%) @1000 μg/mL in Acetonitrile Diallate@1000 μg/mL in Methanol