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Cartap hydrochloride

Cartap hydrochloride Suppliers list
Company Name: Shanghai T&W Pharmaceutical Co., Ltd.  
Tel: +86 21 61551611
Email:
Company Name: Nanjing Sunlida Biological Technology Co., Ltd.  
Tel: 025-57798810 18652991625
Email: sales@sunlidabio.com
Company Name: TianJin Alta Scientific Co., Ltd.  
Tel: 022-65378550-8551
Email: contact@altascientific.com
Company Name: Sigma-Aldrich  
Tel: 021-61415566 800-8193336
Email: orderCN@merckgroup.com
Company Name: Alta Scientific Co., Ltd.  
Tel: 022-6537-8550 15522853686
Email: sales@altasci.com.cn

Cartap hydrochloride manufacturers

Cartap hydrochloride Basic information
Product Name:Cartap hydrochloride
Synonyms:CADAN(R) HYDROCHLORIDE;CARTAP HYDROCHLORIDE;S,S'-[2-(dimethylamino)-1,3-propanediyl] dicarbamothioate hydrochloride;PADAN(R);S,S'2-DIMETHYLAMINOTRIMETHYLENE BIS-(THIOCARBAMATE) HYDROCHLORIDE;SUNTAP(R);SUNVEX(R);VEGETOX(R) HYDROCHLORIDE
CAS:15263-52-2
MF:C7H16ClN3O2S2
MW:273.79
EINECS:239-309-2
Product Categories:Nereistoxin analogue;Alpha sort;C;CA - CGPesticides;CAlphabetic;Insecticides;Pesticides&Metabolites;INSECTICIDE;OLED
Mol File:15263-52-2.mol
Cartap hydrochloride Structure
Cartap hydrochloride Chemical Properties
density 1.4008 (rough estimate)
vapor pressure Negligible
refractive index 1.6100 (estimate)
storage temp. 2-8°C
solubility DMSO (Slightly), Methanol (Slightly), Water (Slightly)
pka7.61 (base)
Water Solubility ca. 200 g l-1 (20 °C, pH 5)
BRN 5157539
Major Applicationagriculture
environmental
InChI1S/C7H15N3O2S2.ClH/c1-10(2)5(3-13-6(8)11)4-14-7(9)12;/h5H,3-4H2,1-2H3,(H2,8,11)(H2,9,12);1H
InChIKeyMSHXTAQSSIEBQS-UHFFFAOYSA-N
SMILESCl[H].CN(C)C(CSC(N)=O)CSC(N)=O
EPA Substance Registry SystemCarbamothioic acid, S,S'-(2-(dimethylamino)-1,3-propanediyl) ester, monohydrochloride (15263-52-2)
Safety Information
Hazard Codes Xn;N,N,Xn
Risk Statements 21/22-50/53
Safety Statements 2-36/37-60-61
RIDADR 2771
WGK Germany 3
RTECS FD1225000
HazardClass 6.1(b)
PackingGroup III
Storage Class6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard ClassificationsAcute Tox. 3 Oral
Acute Tox. 4 Dermal
Aquatic Acute 1
Aquatic Chronic 1
ToxicityLD50 oral in rat: 250mg/kg
MSDS Information
ProviderLanguage
Cartap hydrochloride English
Cartap hydrochloride Usage And Synthesis
DescriptionCartap is a largely obsolete insecticide. It is highly soluble in water, has a low volatility and tends not to persist in soil systems. There are data gaps regarding its human health effects but is known to be moderately toxic. There are also data gaps regarding its ecotoxicity but is highly toxic to aquatic vertebrates and moderately toxic to fish.
Chemical PropertiesFenitrothion is usually made into hydrochloride, the appearance of white crystals, with a slight strange odor. m.p. 183 ~ 183.5 ° C (decomposition) (melting point of the original drug is 179 ~ 181 ° C). Slightly soluble in methanol, insoluble in ethanol, insoluble in organic solvents such as acetone, ether, chloroform, hexane, benzene, etc.; solubility in water is 200g/L at 25°C. It is stable in acidic medium, unstable in alkaline medium. It is stable in acidic medium, unstable in alkaline medium, no change when stored at 40℃ and 60℃ for 3 months, no change when stored in airtight at room temperature, slightly hygroscopic, corrosive to iron and other metals. Its free alkali melting point is 130.5~131℃.
UsesCartap hydrochloride is used to control sucking and chewing insects (particularly Lepidoptera and Coleoptera), at almost all stages of development, on many crops including rice, potatoes, cabbage and other vegetables. It is also used on soya, peanuts, sunflower, maize, sugar beet, wheat, pearl barley, pome, stone and citrus fruit, vines, tea, chestnuts, ginger, cotton and sugar cane.
Production MethodsCartap, commonly formulated as cartap hydrochloride, is produced through a multi-step chemical synthesis involving amination and thiocarbamate formation. The process begins with the reaction of propylene chloride with dimethylamine and an alkali solution at low temperatures, followed by heating to around 45 DegC to complete the amination step. This yields an intermediate compound that is further reacted to cartap hydrochloride.
Agricultural UsesInsecticide: Cartap hydrochloride is used to control chewing and sucking insects on many crops, including rice, potatoes, cabbage and other vegetables, soy beans, peanuts, sunflowers, maize, sugar beet, wheat, pearl barley, pome fruit, stone fruit, citrus fruit, vines, chestnuts, ginger, tea, cotton, and sugar cane. Not currently registered in the U.S. or registered for use in EU countries. There are approximately 15 global suppliers.
Trade nameCADAN®; CALDAN®; KRITAP®; NTD 2®; PADAN®; PATAP®; SANVEX®; THIOBEL®; TI1258®; VEGETOX®
Mechanism of actionPhytotoxic. Nicotinic acetylcholine receptor (nAChR) channel blocker.
Safety ProfilePoison by ingestion andintravenous routes. An experimental teratogen. Aninsecticide. When heated to decomposition it emits verytoxic fumes of NOx, SOx, and HCl.
Metabolic pathwayNereistoxin, 4-N,N-dimethylamino-1,2-dithiolane, is produced from cartap hydrochloride as a main product through photoreaction under UV irradiation in aqueous and methanolic solutions, and on glass and silica gel surfaces. Cartap hydrochloride is also oxidized with N-bromosuccinimide (NBS) to give nereistoxin.
DegradationCartap hydrochloride was hydrolysed to dihydronereistoxin (2) when automatically titrated with sodium hydroxide solution and subsequently oxidised to nereistoxin (3) (see Scheme 1). The hydrolysis was a base catalysed pseudo-first-order reaction with a half-life of 10 minutes at pH 7 and 25 °C. Nereistoxin was so stable that no degradation was observed after 24 hours at 100 °C and with pH in the range 1-4. The DT50 s of nereistoxin at 100 °C and at the higher pH values of 7/10 and 12.3 were 26,20 and 7.9 hours, respectively. It was predicted that nereistoxin (3) would be hydrolysed by alkali to the 3-mercaptopropanesulfenic acid (4) which would be oxidised to the sulfinic acid (5) and thence to the sulfonic acid (6) (Asahi and Yoshida, 1977).
An aqueous solution of unlabelled cartap hydrochloride was exposed to sunlight for a period of 5 days. Analysis was by IR, UV and MS methods. Three products were isolated after irradiation and the major of these was identified as a polymer of nereistoxin (7) and represented 80% of applied dose. The polymer (7) was not toxic to fish (Oryzias latips).
Cartap was hydrolysed to nereistoxin (3) via dihydronereistoxin (2). Nereistoxin (3) was converted into the polymer (7) probably after photolytic formation of a nereistoxin diradical as shown in Scheme 1 (Obayashi and Asaka, 1983).
Pesticide TypeInsecticide
Cartap hydrochloride Preparation Products And Raw materials
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