Scopolamine hydrobromide trihydrate, 99%, Thermo Scientific Chemicals
Scopolamine hydrobromide trihydrate, 99%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Scopolamine hydrobromide trihydrate, 99%, Thermo Scientific Chemicals

Scopolamine hydrobromide trihydrate, CAS # 6533-68-2, is the trihydrate form of scopolamine hydrobromide that shows competitive anti-muscarinic activity by blocking the actions of endogenous acetylcholine or exogenous agonists. It also shows anti-spasmodic and anti-emetic activities.
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25 g
Packaging:
Glass bottle
Catalog number 161750050
Price (USD)/ Each
183.65
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Ends: 31-Dec-2024
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Quantity:
5 g
Packaging:
Glass bottle
Request bulk or custom format
Price (USD)/ Each
183.65
Special Offer
Online exclusive
Ends: 31-Dec-2024
216.00 
Save 32.35 (15%)
Add to cart
Scopolamine hydrobromide trihydrate, 99%, Thermo Scientific Chemicals
Catalog number161750050
Price (USD)/ Each
183.65
Special Offer
Online exclusive
Ends: 31-Dec-2024
216.00 
Save 32.35 (15%)
-
Add to cart
Chemical Identifiers
CAS6533-68-2
IUPAC Namehydrogen (1S,2R,4S,5S)-9-methyl-3-oxa-9-azatricyclo[3.3.1.0²,⁴]nonan-7-yl (2S)-3-hydroxy-2-phenylpropanoate trihydrate bromide
Molecular FormulaC17H28BrNO7
InChI KeyLACQPOBCQQPVIT-FCFGRTKISA-N
SMILES[H+].O.O.O.[Br-].CN1[C@H]2CC(C[C@H]1[C@@H]1O[C@H]21)OC(=O)[C@H](CO)C1=CC=CC=C1
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SpecificationsSpecification SheetSpecification Sheet
Titration with HClO4>=98.5 %
Appearance (Color)Colorless to white
Appearance (Form)Crystalline powder or crystals
Infrared spectrumConforms
Specific optical rotation-24° to -27° (20°C, 589 nm) (c=5, H2O)
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This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

General Information

• Scopolamine hydrobromide trihydrate is a salt form of scopolamine, a tropane alkaloid derived from plants of the nightshade family (Solanaceae), mainly Hyoscyamus niger and Atropa belladonna
• Scopolamine hydrobromide trihydrate, demonstrates competitive anti-muscarinic activity blocking the actions of endogenous acetylcholine or exogenous agonists
• It also shows anti-spasmodic and anti-emetic activities

Applications

• It has been described that scopolamine inhibits muscarinic acetylcholine receptors (mAChRs) with some selectivity for M1 mAChRs
• It is structurally similar to acetylcholine and can antagonize acetylcholine activity mediated by muscarinic receptors located on structures innervated by postganglionic cholinergic nerves and on smooth muscles (that respond to acetylcholine but lack cholinergic innervation)
• Scopolamine hydrobromide trihydrate can induce amnesia in laboratory animals and so it is frequently used in animal models of memory deficit
• Scopolamine hydrobromide trihydrate is used to induce cognitive deficits in animal models of Alzheimer’s disease
• Scopolamine, has been employed in several studies to understand, identify, and characterize biological targets for Alzheimer's disease

RUO – Research Use Only

General References:

  1. Saikia, B.; Barua, c.; Sarma, J. Zanthoxylum alatum ameliorates scopolamine-induced amnesia in rats: Behavioral, biochemical, and molecular evidence. Indian J Pharmacol. 2018, 50, (1), 30–38.
  2. Devore, S.; Almeida,L.; Linster, C. Distinct Roles of Bulbar Muscarinic and Nicotinic Receptors in Olfactory Discrimination Learning. J Neurosci. 2014, 34, (34), 11244–11260.
  3. Venkatesan, R.; Subedi, L. Yeo, E.; Kim, S. Lactucopicrin ameliorates oxidative stress mediated by scopolamine-induced neurotoxicity through activation of the NRF2 pathway. Neurochem Int. 2016, 99, 133-146.
  4. Appenroth, D.; Decker, M.; Tränkle, C.; Mohr, K.; Lehmann, J.; Fleck, C. In vivo investigations on the cholinesterase-inhibiting effects of tricyclic quinazolinimines: Scopolamine-induced cognitive impairments in rats are attenuated at low dosage and reinforced at higher dosage. Pflügers Archiv - European Journal of Physiology. 2008, 455, 895–901.