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| Product | Description | |
|---|---|---|
| ABT-594 | ABT-594, also called as Tebanicline, the (R)-enantiomer of A-98593, is a potent synthetic non-opioid nicotinic analgesic drug. ABT-594 is a novel nAChR ligan which is shown to exert potent analgesic action in models of nociceptive and persistent pain and to possess substantially reduced activity at peripheral nAChRs. Synonyms: 5-[[(2R)-azetidin-2-yl]methoxy]-2-chloropyridine; Tebanicline; ABT-594; ABT 594; ABT594; Ebanicline. CAS No. 198283-73-7. Molecular formula: C9H11ClN2O. Mole weight: 198.65. |  |
| Buprenorphine-3 (BUP) (HRP) | Buprenorphine (or colloquially, "Bupe") is a semi-synthetic opiate with partial agonist and antagonist actions. Buprenorphine hydrochloride was first marketed in the 1980s by Reckitt & Colman (now Reckitt Benckiser) as an analgesic, available generally as Temgesic 0.2 mg sublingual tablets, and as Buprenex in a 0.3 mg/ml injectable formulation. In October 2002, the Food and Drug Administration (FDA) of the United States of America additionally approved Suboxone and Subutex, buprenorphine's high-dose sublingual pill preparations for opioid addiction, and as such the drug is now also used for this purpose. In the USA, it has been a Schedule III drug under the United Nations' Convention on Psychotropic Substances[1] since it was rescheduled from Schedule V (the schedule with the lowest restrictions and penalties in the USA) just before FDA approval of Suboxone and Subutex. In the recent years, buprenorphine has been introduced in most European countries as a transdermal formulation ("patc Group: Biochemicals. Grades: Purified. Pack Sizes: 500ul. US Biological Life Sciences. |  Worldwide |
| Buprenorphine (BSA) | Buprenorphine (or colloquially, "Bupe") is a semi-synthetic opiate with partial agonist and antagonist actions. Buprenorphine hydrochloride was first marketed in the 1980s by Reckitt & Colman (now Reckitt Benckiser) as an analgesic, available generally as Temgesic 0.2mg sublingual tablets, and as Buprenex in a 0.3mg/ml injectable formulation. In October 2002, the Food and Drug Administration (FDA) of the United States of America additionally approved Suboxone and Subutex, buprenorphine's high-dose sublingual pill preparations for opioid addiction, and as such the drug is now also used for this purpose. In the USA, it has been a Schedule III drug under the United Nations' Convention on Psychotropic Substances since it was rescheduled from Schedule V (the schedule with the lowest restrictions and penalties in the USA) just before FDA approval of Suboxone and Subutex. In the recent years, buprenorphine has been introduced in most European countries as a transdermal formulation ("patch") f Group: Biochemicals. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Buprenorphine (BUP) (BSA) | Buprenorphine (or colloquially, "Bupe") is a semi-synthetic opiate with partial agonist and antagonist actions. Buprenorphine hydrochloride was first marketed in the 1980s by Reckitt & Colman (now Reckitt Benckiser) as an analgesic, available generally as Temgesic 0.2 mg sublingual tablets, and as Buprenex in a 0.3 mg/ml injectable formulation. In October 2002, the Food and Drug Administration (FDA) of the United States of America additionally approved Suboxone and Subutex, buprenorphine's high-dose sublingual pill preparations for opioid addiction, and as such the drug is now also used for this purpose. In the USA, it has been a Schedule III drug under the United Nations' Convention on Psychotropic Substances[1] since it was rescheduled from Schedule V (the schedule with the lowest restrictions and penalties in the USA) just before FDA approval of Suboxone and Subutex. In the recent years, buprenorphine has been introduced in most European countries as a transdermal formulation ("patc Group: Biochemicals. Grades: Purified. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Remifentanil Impurity 1 ( RTF-02) | An impurity of Remifentanil. Remifentanil is a synthetic opioid analgesic drug. It is given to patients during surgery to relieve pain and as an adjunct to an anaesthetic. Synonyms: SCHEMBL3167494; Methyl 4-cyano-4-(phenylamino)-1-piperidinepropanoate; REMIFENTANIL HYDROCHLORIDE IMPURITY M [EP IMPURITY]; 1-Piperidinepropanoic acid, 4-cyano-4-(phenylamino)-, methyl ester. Grades: > 95%. CAS No. 938184-94-2. Molecular formula: C16H21N3O2. Mole weight: 287.36. | |
| Remifentanil Impurity 4 | An intermediate in the preparation of Fentanyl analogues. Remifentanil is a synthetic opioid analgesic drug. It is given to patients during surgery to relieve pain and as an adjunct to an anaesthetic. Synonyms: 4-[(1-Oxopropyl)phenylamino]-4-piperidinecarboxylic Acid Methyl Ester. Grades: > 95%. CAS No. 72996-78-2. Molecular formula: C16H22N2O3. Mole weight: 290.37. | |
| Zomepirac Sodium | Zomepirac sodium salt is a prostaglandin synthetase inhibitor, was indicated for the management of mild to severe pain. Uses: An analgesic, anti-inflammatory drug. Synonyms: 5-(4-Chlorobenzoyl)-1,4-dimethyl-1H-pyrrole-2-acetic Acid Sodium Salt; McN 2783-21-98; 2-[5-(4-chlorobenzoyl)-1,4-dimethyl-1H-pyrrol-2-yl]acetic acid. Grades: ≥98%. CAS No. 64092-48-4. Molecular formula: C15H13ClNNaO3. Mole weight: 313.71. | |
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