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505818 Scopolamine Hydrobromide - CAS 114-49-8 - Calbiochem

MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

Synonyms: Muscarinic Acetylcholine Receptor (mAChR) Antagonist, Scopolamine, Levo-duboisine, Hyoscine, Scopoderm

505818
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Overview

Replacement Information

Key Specifications Table

Empirical FormulaCAS #
C₁₇H₂₁NO₄•HBr 114-49-8

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      Description
      OverviewA competitive, non-selective antagonist for muscarinic acetylcholine receptors (mAChR). Most effective at treating motion sickness. It is also a research tool for inducing memory impairment in vivo. Frequently used in researches related to learning, memory and Alzheimer′s dementia.
      Catalogue Number505818
      Brand Family Calbiochem®
      SynonymsMuscarinic Acetylcholine Receptor (mAChR) Antagonist, Scopolamine, Levo-duboisine, Hyoscine, Scopoderm
      References
      ReferencesKlinkenberg, I., et al. 2010. Neurosci Biobehav Rev 34, 1307.
      Aparkes. W. 1995. Psychopharmacologia. 7, 1.
      Product Information
      CAS number114-49-8
      FormOff-white solid
      Hill FormulaC₁₇H₂₁NO₄•HBr
      Chemical formulaC₁₇H₂₁NO₄•HBr
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Purity≥99% by HPLC
      Physicochemical Information
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      R PhraseR: 22-45-62-63

      Harmful if swallowed.
      May cause cancer.
      Possible risk of impaired fertility.
      Possible risk of harm to the unborn child.
      S PhraseS: 36/37/39-45-46

      Wear suitable protective clothing, gloves and eye/face protection.
      In case of accident or if you feel unwell, seek medical advice immediately (show the label where possible).
      If swallowed, seek medical advice immediately and show this container or label.
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
      Toxicity Harmful
      Storage +2°C to +8°C
      Protect from Light Protect from light
      Do not freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
      Packaging Information
      Transport Information
      Supplemental Information
      Specifications

      Documentation

      Scopolamine Hydrobromide - CAS 114-49-8 - Calbiochem SDS

      Title

      Safety Data Sheet (SDS) 

      References

      Reference overview
      Klinkenberg, I., et al. 2010. Neurosci Biobehav Rev 34, 1307.
      Aparkes. W. 1995. Psychopharmacologia. 7, 1.
      Data Sheet

      Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

      Revision15-November-2013 JSW
      SynonymsMuscarinic Acetylcholine Receptor (mAChR) Antagonist, Scopolamine, Levo-duboisine, Hyoscine, Scopoderm
      DescriptionA competitive, non-selective antagonist for muscarinic acetylcholine receptors (mAChR). Most effective at treating motion sickness. It is also a research tool for inducing memory impairment in vivo. Frequently used in researches related to learning, memory and Alzheimer′s dementia.
      FormOff-white solid
      CAS number114-49-8
      Chemical formulaC₁₇H₂₁NO₄•HBr
      Structure formulaStructure formula
      Purity≥99% by HPLC
      SolubilityH₂O (100 mM)
      Storage +2°C to +8°C
      Protect from light
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
      Toxicity Harmful
      ReferencesKlinkenberg, I., et al. 2010. Neurosci Biobehav Rev 34, 1307.
      Aparkes. W. 1995. Psychopharmacologia. 7, 1.