- Tiamenidine
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2026-05-11
- CAS:31428-61-2
- Purity:
- Supply Ability: 10g
- Tiamenidine
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2020-05-10
- CAS:31428-61-2
- Min. Order: 1KG
- Purity: 99.0%
- Supply Ability: 500 MT
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| | Tiamenidine Basic information |
| Product Name: | Tiamenidine | | Synonyms: | Tiamenidine;Sundralen;Thiamenidine;2-[(2-Chloro-4-methyl-3-thienyl)amino]-2-imidazoline;N-(2-Chloro-4-methyl-3-thienyl)-4,5-dihydro-1H-imidazol-2-amine;N-(2-Chloro-4-Methylthiophen-3-yl)-4,5-dihydro-1H-iMidazol-2-aMine;HOE-440;N-(2-Chloro-4-methyI-3-thienyl)-4，5-dihydro-1H-imidazol-2-amine | | CAS: | 31428-61-2 | | MF: | C8H10ClN3S | | MW: | 215.7 | | EINECS: | | | Product Categories: | | | Mol File: | 31428-61-2.mol |  |
| | Tiamenidine Chemical Properties |
| Melting point | 152° | | Boiling point | 305.1±52.0 °C(Predicted) | | density | 1.52±0.1 g/cm3(Predicted) | | storage temp. | 2-8°C | | pka | 8.53±0.10(Predicted) |
| | Tiamenidine Usage And Synthesis |
| Chemical Properties | Crystallized from methylcyclohexane and benzene, melting point 152°C. Tiamenidine hydrochloride (Tiamenidilie Hydrochloride): C8H10ClN3SHCl.[51274-83-0]. Crystallized from isopropanol-petroleum ether, melting point 228-229°C. Acute toxicity LD50 mice, rats (mg/kg): 45, 40 IV. Acute toxicity LD50 mice (mg/kg): 170 subcutaneous; 400 oral. | | Uses | Tiamenidine is an α2-adrenergic receptor agonist used as an antihypertensive. | | Definition | ChEBI: Tiamenidine is an organochlorine compound. |
| | Tiamenidine Preparation Products And Raw materials |
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