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J & K SCIENTIFIC LTD.
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Product Name:FenoldopaM HydrobroMide CAS:67287-54-1 Package:100Mg,10Mg
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Chemsky (shanghai) International Co.,Ltd
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Product Name:FenoldopaM HydrobroMide;6-Chloro-2,3,4,5-tetrahydro-1-(4-hydroxyphenyl)-1H-3-benzazepine-7,8-diol HydrobroMide; (±)-FenoldopaM HydrobroMide; (±)-SKF 82526 HydrobroMide; SKF 82526 HydrobroMide; CAS:67287-54-1 Purity:98+% Package:1Mg;5Mg;10Mg;50Mg;100Mg;500Mg
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Guangzhou Isun Pharmaceutical Co., Ltd
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Product Name:FenoldopaM MonohydrobroMide CAS:67287-54-1 Purity:>=98% Package:25Mg; 1g; 100g; 500g
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Sigma-Aldrich
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CAS:67287-54-1
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| 6-chloro-2,3,4,5-tetrahydro-7,8-dihydroxy-1-(4-hydroxyphenyl)-1H-3-benzazepinium bromide Basic information |
Product Name: | 6-chloro-2,3,4,5-tetrahydro-7,8-dihydroxy-1-(4-hydroxyphenyl)-1H-3-benzazepinium bromide | Synonyms: | (±)-SKF 82526 HydrobroMide;6-Chloro-2,3,4,5-tetrahydro-1-(4-hydroxyphenyl)-1H-3-benzazepine-7,8-diol HydrobroMide;SKF 82526 HydrobroMide;6-chloro-2,3,4,5-tetrahydro-7,8-dihydroxy-1-(4-hydroxyphenyl)-1H-3-benzazepinium bromide;FENOLDOPAM MONOHYDROBROMIDE;6-chloro-2,3,4,5-tetrahydro-1-(4-hydroxyphenyl)-1h-3-benzazepine-7,8-diol monohydrobromide;FenoldopaM HydrobroMide;Fenoldopam Monohydrobromide
DISCONTINUED, offer F248790 | CAS: | 67287-54-1 | MF: | C16H16ClNO3.BrH | MW: | 386.67 | EINECS: | 266-634-7 | Product Categories: | Agonists;Aromatics;Heterocycles;Intermediates & Fine Chemicals;Neurochemicals;Pharmaceuticals | Mol File: | 67287-54-1.mol | |
| 6-chloro-2,3,4,5-tetrahydro-7,8-dihydroxy-1-(4-hydroxyphenyl)-1H-3-benzazepinium bromide Chemical Properties |
Melting point | >233°C (dec.) | storage temp. | 2-8°C | solubility | DMSO: >12mg/mL | form | Solid | color | off-white |
| 6-chloro-2,3,4,5-tetrahydro-7,8-dihydroxy-1-(4-hydroxyphenyl)-1H-3-benzazepinium bromide Usage And Synthesis |
Uses | Fenoldopam Monohydrobromide is a potent D-1 dopamine agonists. | Uses | Dopamine D1-receptor agonist. Antihypertensive. | Biochem/physiol Actions | Fenoldopam is a selective dopamine agonist that is being considered for the parenteral treatment of systemic hypertension. In both an oral and parenteral form, fenoldopam causes peripheral vasodilation by stimulating dopamine-1 adrenergic receptors. Intravenous fenoldopam may provide advantages over sodium nitroprusside because it can induce both a diuresis and natriuresis, is not light sensitive, and is not associated with cyanide toxicity. There is no evidence for rebound hypertension after discontinuation of fenoldopam infusion. |
| 6-chloro-2,3,4,5-tetrahydro-7,8-dihydroxy-1-(4-hydroxyphenyl)-1H-3-benzazepinium bromide Preparation Products And Raw materials |
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