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| Product | Description | |
|---|---|---|
| Dexmedetomidine | α2-Adrenergic agonist; (+)-isomer of Medetomidine; sedative; analgesic. Group: Biochemicals. Alternative Names: 5-[(1S)-1-(2,3-Dimethylphenyl)ethyl]-1H-imidazole; (S)-4-[1-(2,3-Dimethylphenyl)ethyl]-1H-imidazole; (+)-Medetomidine; (S)-Medetomidine; MPV 1440; d-Medetomidine. Grades: Highly Purified. CAS No. 113775-47-6. Pack Sizes: 10mg, 50mg, 100mg, 250mg. US Biological Life Sciences. |  Worldwide |
| Dexmedetomidine | Dexmedetomidine ((+)-Medetomidine) is a potent, selective and orally active agonist of α2-adrenoceptor , with a K i of 1.08 nM. Dexmedetomidine shows 1620-fold selectivity against α1-adrenoceptor. Dexmedetomidine exhibits anxiolysis, sedation, and modest analgesia effects [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (+)-Medetomidine; (S)-Medetomidine. CAS No. 113775-47-6. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-12719. |  |
| Dexmedetomidine HCl | 4-[(1S)-1-(2,3-Dimethylphenyl)ethyl]-1H-imidazole hydrochloride. CAS No. 145108-58-3. Product ID: 8-04655. Molecular formula: C13H16N2·HCl. Mole weight: 236.74. |  |
| Dexmedetomidine HCl | Dexmedetomidine HCl. Group: Biochemicals. Grades: Highly Purified. CAS No. 145108-58-3. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C13H17ClN2. US Biological Life Sciences. | Worldwide |
| Dexmedetomidine hydrochloride | Dexmedetomidine hydrochloride, 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; Dexmedetomidine hydrochloride; 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: Dexmedetomidine hydrochloride, 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 |  |
| Dexmedetomidine hydrochloride | Dexmedetomidine hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 145108-58-3. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Dexmedetomidine hydrochloride | Dexmedetomidine hydrochloride ((+)-Medetomidine hydrochloride) is a potent, selective and orally active agonist of α2-adrenoceptor , with a K i of 1.08 nM. Dexmedetomidine hydrochloride shows 1620-fold selectivity against α1-adrenoceptor. Dexmedetomidine hydrochloride 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. | |
| 1-? (2, ?3-?Dimethylphenyl) ?ethanol | 1-? (2, ?3-?Dimethylphenyl) ?ethanol is a reagent used in the synthesis of α-adrenoreceptor agonist used in veterinary medicine for its analgesic and sedative activity. Dexmedetomidine (D299000), an α2-Adrenergic agonist, impurity. Group: Biochemicals. Grades: Highly Purified. CAS No. 60907-90-6. Pack Sizes: 50mg, 100mg. Molecular Formula: C10H14O, Molecular Weight: 150.22. US Biological Life Sciences. | Worldwide |
| 1-Hydroxy N-Trityl Medetomidine-d3 | 1-Hydroxy N-Trityl Medetomidine-d3 is an intermediate in the synthesis of Dexmedetomidine-d4 L-Tartrate (d4-Major) (D299006). Dexmedetomidine-d4 L-Tartrate is the labeled salt analogue of Dexmedetomidine (D299000), an α2-Adrenergic agonist; (+)-isomer of Medetomidine; sedative; analgesic. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg, 25mg. Molecular Formula: C32H27D3N2O. US Biological Life Sciences. | Worldwide |
| 1-Triphenyl methyl imidazole-4-carboxylic Acid-d2 | 1-Triphenyl methyl imidazole-4-carboxylic Acid-d2, is the labeled analogue of 1-Triphenyl methyl imidazole-4-carboxylic Acid (T889200), used as an intermediate for the synthesis of labeled Dexmedetomidine (D299000), a sedative and analgesic. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C23H16D2N2O2, Molecular Weight: 356.41. US Biological Life Sciences. | Worldwide |
| 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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