- Amobam
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- $1.00
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2024-07-20
- CAS:3566-10-7
- Min. Order: 1Kg
- Purity: 98%
- Supply Ability: 20T
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| Product Name: | AMOBAM | | Synonyms: | AMOBAM (TM);AMOBAM;Amobam aqueous solution;CHEM-O-BAM(R);CHEM-O-BAM;ETHYLENE BIS(DITHIOCARBAMIC ACID) DI-AMMONIUM SALT;ethylenebis(dithio-carbamicacidiammoniumsalt;Stainless | | CAS: | 3566-10-7 | | MF: | C4H14N4S4 | | MW: | 246.44 | | EINECS: | 222-651-1 | | Product Categories: | | | Mol File: | 3566-10-7.mol |  |
| | AMOBAM Chemical Properties |
| Melting point | 185 °C(Solv: ethanol (64-17-5)) | | solubility | DMSO (Slightly), Methanol (Slightly) | | form | Solid | | color | White to Off-White | | Stability: | Temperature Sensitive, Very Hygroscopic | | EPA Substance Registry System | Diammonium ethylenebis(dithiocarbamate) (3566-10-7) |
| TSCA | TSCA listed | | Toxicity | LD50 orl-rat: 395 mg/kg 28ZEAL 5,11,76 |
| | AMOBAM Usage And Synthesis |
| Description | This substance is an obsolete carbamate fungicide. Very little data relating to its environmental fate, ecotoxicity or impact on human health is available. | | Chemical Properties | Pure white colorless crystal. Melting point 72.5-72.8℃. The original drug is orange or light yellow aqueous solution, weak alkaline, with ammonia and hydrogen sulfide odor. Soluble in water, slightly soluble in ethanol, acetone, insoluble in benzene. Unstable in air, aqueous solution is more stable chemically, but it is easy to decompose when the temperature is higher than 40℃, and it is also easy to decompose when it meets acidic substances. | | Uses | Amobam is a fungicidal compound which is used to protect and treat vegetation. Pesticide. | | Definition | ChEBI: A dithiocarbamate salt resulting from the formal reaction of ethylenebis(dithiocarbamic acid) with 2 mol eq. of ammonia. A water-soluble crystalline solid, it is a fungicide used to protect fruit, vegetable, and field crops against a wide spectrum of funga
diseases. Mixing amobam with zinc sulfate affords the fungicide zineb. | | Production Methods | Diammonium ethylenebis(dithiocarbamate) would have been produced using the same industrial chemistry applied to other EBDC fungicides such as maneb, zineb, and nabam. Commercial manufacture began with ethylene diamine, which was reacted with carbon disulphide under alkaline conditions to form the ethylenebis(dithiocarbamate) anion. Neutralisation with ammonium salts yielded the diammonium form rather than the metal complexed EBDCs used more widely in agriculture. | | Mechanism of action | Non-specific, inhibts respiration. | | Safety Profile | Poison by ingestion. When heatedto decomposition it emits very toxic fumes of SOx andNOx. | | Pesticide Type | Fungicide |
| | AMOBAM Preparation Products And Raw materials |
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