| Alprazolam |
![]() Last updated: 10/10/2025 |
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(Not known by any other names) |
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A veterinary and human benzodiazepine drug commonly used to control various anxiety disorders | |
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A sedative/tranquilizer used as an adjunctive therapy to treat anxiety or panic. | |
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Dogs; Cats |
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Not approved | |
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Not approved |
| Chemical structure |
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None | |
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C₁₇H₁₃ClN₄ | |
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CC1=NN=C2N1C3=C(C=C(C=C3)Cl)C(=NC2)C4=CC=CC=C4 | |
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VREFGVBLTWBCJP-UHFFFAOYSA-N | |
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InChI=1S/C17H13ClN4/c1-11-20-21-16-10-19-17(12-5-3-2-4-6-12)14-9-13(18)7-8-15(14)22(11)16/h2-9H,10H2,1H3 | |
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Yes |
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| Common Name | Relationship | Link |
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| alprazolam dihydrate | Hydrate | ![]() |
| alprazolam | - | ![]() |
| General status |
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Medicinal drug: Tranquiliser; Sedative | ||||||||||||||
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Benzodiazepine | ||||||||||||||
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Synthetic | ||||||||||||||
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[GABA-A receptor (anion channel), Modulator] | ||||||||||||||
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28981-97-7 | ||||||||||||||
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249-349-2 | ||||||||||||||
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2118 | ||||||||||||||
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Nervous system: Benzodiazepine derivatives | ||||||||||||||
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QN05BA12 | ||||||||||||||
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UK: Class C, Schedule 4 Pt1; EU: UN71, Class IV | ||||||||||||||
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308.77 | ||||||||||||||
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8-chloro-1-methyl-6-phenyl-4H-(1,2,4)triazolo(4,3-α)(1,4)benzodiazepine | ||||||||||||||
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8-chloro-1-methyl-6-phenyl-4H-s-triazolo(4,3-a)(1,4)benzodiazepine | ||||||||||||||
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May react with other medications | ||||||||||||||
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Current | |||
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Circa 1969, introduced | |||
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Usually available in both solid and liquid forms. Often human medications are used for animals, off-label | |||
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The production of alprazolam involves a multi-step chemical synthesis centred around constructing its triazolobenzodiazepine core. It typically begins with the preparation of 2-amino-5-chlorobenzophenone, which undergoes acylation with chloroacetyl chloride to form a key intermediate. This is followed by cyclisation using reagents like hexamethylenetetramine and hydrochloric acid to build the diazepine ring. The resulting compound is then treated with nitric acid and sodium bicarbonate to refine its structure and adjust pH, forming nordazepam-like intermediates. Finally, a triazole ring is introduced through condensation with hydrazine derivatives, yielding alprazolam. | |||
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Published GHG data is not available for most pharmaceuticals. However, according to industry, global averages suggest producing 1 kg of a typical active pharmaceutical ingredient can range from 10 to 100 kg CO₂e for small molecule drugs and potentially up to 1000 kg CO₂e for complex biologicals such as vaccines, depending on the drug type, its formulation, complexity of synthesis, solvent recovery, and energy sources used. |
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13.1 | V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) 3 = Unverified data of known source |
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1.32 X 1002 | Calculated | - | |||||||
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2.12 | V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) 3 = Unverified data of known source |
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As this parameter is not normally measured directly, a surrogate measure is used: ‘Photochemical oxidative DT₅₀’. Where data is available, this can be found in the Fate Indices section below. | ||||||||||
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| Known metabolites |
None
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| Terrestrial ecotoxicology |
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770 | V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) Mouse3 = Unverified data of known source |
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| General |
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770 | V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) Mouse3 = Unverified data of known source |
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Intraperitoneal LD₅₀ = 380 mg kg⁻¹ | V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) Mouse3 = Unverified data of known source |
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| Subcutaneous LD₅₀ > 5000 mg kg⁻¹ | V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) Mouse3 = Unverified data of known source |
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Hepatic metabolism via cytochrome P450 3A4 with renal excretion | V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) 3 = Unverified data of known source |
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| Health issues |
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May cause over sedation and loss of motor control CNS toxicant May cuase over excitment and aggression |
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| Handling issues |
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No information available | |||
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Health: H302, H360, H362, H336 | |||
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Not listed (Not listed) | |||
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alprazolam | ||
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| Record last updated: | 10/10/2025 |
| Contact: | aeru@herts.ac.uk |
| Please cite as: | Lewis, K.A., Tzilivakis, J., Warner, D. and Green, A. (2016) An international database for pesticide risk assessments and management. Human and Ecological Risk Assessment: An International Journal, 22(4), 1050-1064. DOI: 10.1080/10807039.2015.1133242 |
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