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Dexmedetomidinehydrochloride, a highly selective adrenergic receptor agonist, is used primarily for sedation during tracheal intubation and mechanical ventilation in patients undergoing hand-2 surgery under general anesthesia, and for sedation in patients initiating intubation and ventilator use during intensive care. Synonyms: 4- [ (1r) -1- (2, 3-di methyl phenyl) ethyl] -3h-imidazole hydrochloride ; 4- ( (s) -alpha, 2, 3-tri methyl benzyl) imidazolemono hydrochloride ; DEXMEDETOMIDINEHCL; DEXMEDETOMIDINE hydROCHLChemicalbookORide ; DEMEDETOMIDINEHCL; Dexmedetomidine (Pilot) ; 4- [ (1S) -1- (2, 3-Di methyl phenyl) ethyl] -1H-imidazole hydrochloride ; 4- ( (S) -?, 2, 3-Tri methyl benzyl) imidazolemono hydrochloride . CAS No. 145108-58-3. Product ID: PAP-0085. Molecular formula: C13H17ClN2. Category: sedative. Product Keywords: Other Active Pharmaceutical Ingredients; Dexmedetomidinehydrochloride; PAP-0085; sedative; C13H17ClN2; 145108-58-3. Standard: CP. Chemical Name: 4-[(1r)-1-(2,3-dimethylphenyl)ethyl]-3h-imidazolehydrochloride. Grade: Pharmaceutical Grade. Solubility: H2O: soluble20mg/mL, clear. Storage: 2-8°C. Melting Point: 156.5-157.5°. Product Description: Dexmedetomidinehydrochloride, a highly selective adrenergic receptor agonist, is used primarily for sedation during tracheal intubation and mechanical ventilation in patients undergoing hand-2 surgery under general anesthesia, and for sedation in patients initiating intubation and ventilato
Dexmedetomidinehydrochloride
Dexmedetomidinehydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 145108-58-3. Pack Sizes: 10mg, 50mg. US Biological Life Sciences.
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Dexmedetomidinehydrochloride
Dexmedetomidinehydrochloride ((+)-Medetomidine hydrochloride) is a potent, selective and orally active agonist of α2-adrenoceptor , with a K i of 1.08 nM. Dexmedetomidinehydrochloride shows 1620-fold selectivity against α1-adrenoceptor. Dexmedetomidinehydrochloride exhibits anxiolysis, sedation, and modest analgesia effects [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (+)-Medetomidine hydrochloride; (S)-Medetomidine hydrochloride. CAS No. 145108-58-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-17034A.
Dexmedetomidine Impurity A HCl
Dexmedetomidine Impurity A HCl. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 4-(1-(3,4-dimethylphenyl)ethyl)-1H-imidazole hydrochloride. Molecular Formula: C13H17ClN2. Mole Weight: 236.74. Catalog: APB04853.
Dexmedetomidine Impurity C HCl
Dexmedetomidine Impurity C HCl. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 4,5-bis(1-(2,3-dimethylphenyl)ethyl)-1H-imidazole hydrochloride. Molecular Formula: C23H29ClN2. Mole Weight: 368.94. Catalog: APB04852.
Dexmedetomidine Impurity D HCl
Dexmedetomidine Impurity D HCl. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 2-(1-(2,3-dimethylphenyl)ethyl)-1H-imidazole hydrochloride. Molecular Formula: C13H16N2·HCl. Mole Weight: 236.74. Catalog: APB04851.
Dexmedetomidine Impurity E HCl
Dexmedetomidine Impurity E HCl. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 1-(1-(2,3-dimethylphenyl)ethyl)-1H-imidazole hydrochloride. Molecular Formula: C13H17ClN2. Mole Weight: 236.74. Catalog: APB04849.
MK-467
MK-467 is a peripheral Alpha2 -adrenoceptor antagonist originated by Merck & Co. It can dose-dependently attenuate the bradycardia associated with dexmedetomidine, and shorten the sedative effect without altering its quality. Clinical for Diabetes mellitus in USA was discontinued in 1994. Uses: Diabetes mellitus. Synonyms: MK-467; MK 467; MK467; UNII-66932R910R; N-(2-((2R,12bS)-2'-oxo-1,3,4,6,7,12b-hexahydrospiro[benzofuro[2,3-a]quinolizine-2,4'-imidazolidin]-3'-yl)ethyl)methanesulfonamide hydrochloride. Grades: 98%. CAS No. 130466-38-5. Molecular formula: C20H27ClN4O4S. Mole weight: 454.98.
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