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ALDICARB-SULFONE

ALDICARB-SULFONE Structure
CAS No.
1646-88-4
Chemical Name:
ALDICARB-SULFONE
Synonyms
ALDOXYCARB;UCES;ent4.9;Standak;STANDOK;UC21865;Sulfocarb;STANDAK(R);aldoxycarbe;YangdiMiewei
CBNumber:
CB7710151
Molecular Formula:
C7H14N2O4S
Molecular Weight:
222.26
MOL File:
1646-88-4.mol
MSDS File:
SDS
Modify Date:
2024/7/2 8:55:17

ALDICARB-SULFONE Properties

Melting point 132-135 °C
Density 1.3816 (rough estimate)
vapor pressure 1.2×10-2 Pa (25 °C)
refractive index 1.5690 (estimate)
storage temp. 0-6°C
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
Water Solubility 10 g l-1 (25 °C)
pka 13.44±0.46(Predicted)
color White to Off-White
BRN 2215242
EPA Substance Registry System Aldicarb sulfone (1646-88-4)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06,GHS09
Signal word  Danger
Hazard statements  H300+H310+H330-H400
Precautionary statements  P260-P262-P273-P280-P302+P352+P310-P304+P340+P310
Hazard Codes  T+
Risk Statements  24-26/28
Safety Statements  28-36/37-45
RIDADR  2757
WGK Germany  3
RTECS  UE2080000
HazardClass  6.1(a)
PackingGroup  I
Toxicity duck,LD50,oral,33500ug/kg (33.5mg/kg),Pesticide Manual. Vol. 9, Pg. 18, 1991.
NFPA 704
0
4 0

ALDICARB-SULFONE Chemical Properties,Uses,Production

Description

Aldoxycarb, is also called 2-mesyl-2-methylpropionaldehyde O-methylcarbamoyloxime (IUPAC), the sulfone analog of aldicarb, is also a systemic insecticide effective for control of insects (mainly sucking insect pests such as aphids, leafhoppers, etc.).

Chemical Properties

Aldoxycarb is a carbamate pesticide used mainly as an insecticide and acaricide. It is a white crystalline powder with a slightly sulfurous odor. Aldoxycarb is extremely toxic to wildlife. Aldoxycarb (Aldicarb sulfone) is a breakdown product of aldicarb. Aldoxycarb is a degradate/metabolite of aldicarb produced by the oxidation of the thio-moiety.

Uses

Aldicarb Sulfone is an analog of Aldicarb (A514650) detected in agricultural products as pesticide residue.

General Description

White crystalline solid. Insecticide.

Reactivity Profile

ALDICARB-SULFONE is a carbamate ester. Carbamates are chemically similar to, but more reactive than amides. Like amides they form polymers such as polyurethane resins. Carbamates are incompatible with strong acids and bases, and especially incompatible with strong reducing agents such as hydrides. Flammable gaseous hydrogen is produced by the combination of active metals or nitrides with carbamates. Strongly oxidizing acids, peroxides, and hydroperoxides are incompatible with carbamates.

Health Hazard

Exposures to high levels of aldoxycarb cause adverse health effects and damages the nervous system of humans and laboratory animals. Chemicals that cause adverse health effects in humans and laboratory animals after high levels of exposure may pose a risk of adverse health effects in humans exposed to lower levels over long periods of time. Ingestion and other exposures to the chemical cause various health disorders. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure. The symptoms include, but are not limited to, eye irritation, skin irritation, dizziness, sweating, malaise, CNS depression, abdominal pain, diarrhea, nausea, vomiting, salivation, headache, ataxia, muscle twitching, muscle weakness, runny nose, tearing eyes, pinpoint pupils or dark vision, wheezing, increased or decreased heart rate, seizures, convulsions, and death. It has not caused any delayed neurotoxicity in animals. The onset of these symptoms is rapid and the severity of symptoms depends on the dose. The immediate cause of death is usually respiratory failure.

Agricultural Uses

Insecticide, Acaricide, Nematicide: Used to control honey locust, gall midge and other insects and mites on cotton, potatoes, sugar beets and ornamentals. Applied to the soil by soluble mixture or spikes. Not listed for use in EU countries.

Trade name

ALDICARB SULFONE®; TEMIK SULFONE®; SULFOCARB®; STANDAK®; UC-21865®

Metabolic pathway

Aldoxycarb is the sulfone analogue of aldicarb. It has now been superseded but, because of its close relationship with aldicarb, it is included here. The degradation and metabolic pathway of these two structurally related compounds are consistent with each other. Information on the metabolism of aldoxycarb discussed in this summary is based on results obtained from studies where aldoxycarb was the test substance. Additional information can be obtained from the aldicarb summary. The metabolism of aldoxycarb in soils, plants and animals follow common metabolic pathways which include the hydrolysis and elimination of the oxime carbamate to yield the corresponding oximes and nitriles. These primary metabolites are further degraded via hydrolysis to the corresponding amides and acids. Other reactions also include the hydrolysis/ oxidation of the oxime to the corresponding alcohol, aldehyde and acid. Further degradation to methane sulfonic acid was observed in plants and animals. The metabolic pathways of aldoxycarb are presented in Scheme 1.

ALDICARB-SULFONE Preparation Products And Raw materials

Global( 89)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29826 58 Inquiry
AFINE CHEMICALS LIMITED +86-0571-85134551 China 15395 58 Inquiry
Shaanxi Didu New Materials Co. Ltd +86-89586680 +86-13289823923 China 9003 58 Inquiry
Hebei Duling International Trade Co. LTD +8617333973358 China 15438 58 Inquiry
TargetMol Chemicals Inc. +1-781-999-5354 United States 19973 58 Inquiry
SUZHOU SENFEIDA CHEMICAL CO.,LTD +86-0512-83500002 +8615195660023 China 10814 58 Inquiry
Shanghai Acmec Biochemical Technology Co., Ltd. +undefined18621343501 China 33350 58 Inquiry
Aladdin Scientific +1-+1(833)-552-7181 United States 57511 58 Inquiry
LGC Standards +44 (0)20 8943 8480 United Kingdom 6495 0 Inquiry
ALDICARB-SULFONE PESTANAL ENDOSULFAN LACTONE PESTANAL, 100 MG (1E)-2-Methyl-1-(([(methylamino)carbonyl]oxy)imino)-2-(methylsulfonyl)propane 2-mesyl-2-methylpropionaldehydeo-methylcarbamoyloxime ALDOXYCARB, 10MG, NEAT Aldicarb sulfone 10mg [1646-88-4] Aldoxycarb 10mg [1646-88-4] UCES YangdiMiewei Propanal,2-methyl-w-(methyl-sulfonyl)-O-[(methylamino)carbonyl]oxime AldicarbSulrone 2-methyl-2-(methylsulfonyl)-propionaldehydo-(methylcarbamoyl)oxime aldoxycarbe Carbamic acid, methyl-, O-[[2-methyl-2-(methylsulfonyl)propylidene]amino] deriv. ent4.9 entai3-29261 Propanal, 2-methyl-2-(methylsulfonyl)-, O-[(methylamino)carbonyl]oxime Propionaldehyde, 2-methyl-2-(methylsulfonyl)-, O-(methylcarbamoyl)oxime Standak Sulfocarb Temik sulfone 2-METHYL-2-(METHYLSULFONYL)PROPANAL-O-[(METHYLAMINO)CARBONYL]OXIME 2-METHYL-2-(METHYLSULFONYL)-PROPIONALDEHYDE O-(METHYLCARBAMOYL)-OXIME ALDICARB-SULFONE ALDICARB SULPHONE STANDOK STANDAK(R) UC21865 2-methyl-2-(methylsulphonyl)propionaldehyde O-(methylcarbamoyl)oxime ALDICARB SULFONE(TEMIK SULFONE) AldicarbSulfoneSolution,2000mg/L,1ml AldicarbSulfoneSolution,10mg/L,1ml AldicarbSulfoneSolution,100mg/L,1ml Aldicarb sulfone Solution in Acetonitrile, 1000μg/mL Aldicarb sulfone Solution in Methanol, 100μg/mL Aldicarb sulfone Solution in Methanol, 1000μg/mL ALDOXYCARB Aldicarb sulfone,Cholinesterase (ChE),inhibit,Inhibitor 1646-88-4 A AA to ALPesticides A-BAlphabetic Alpha sort CarbamatesEnvironmental Standards Insecticides MetabolitesPesticides&Metabolites Nematicides Pesticides Pesticides&Metabolites