505016 CX546 - CAS 215923-54-9 - Calbiochem

CX546 - CAS 215923-54-9 - Calbiochem MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

Synonyms: AMPA Positive Allosteric Modulator, CX546, CX-546, CX 546

Primary Target: AMPA
505016
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      Overview

      Replacement Information

      Key Specifications Table

      Empirical FormulaCAS #
      C₁₄H₁₇NO₃ 215923-54-9

      Pricing & Availability

      Catalog Number AvailabilityPackaging Qty/Pack Price Quantity
      5.05016.0001
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          		 Glass bottle 10 mg
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          Description
          OverviewA positive allosteric modulator selective for the AMPA receptors. Used in studies related to Schizophrenia, neuroplasticity, Autism and neuronal differentiation.
          Catalogue Number505016
          Brand Family Calbiochem®
          SynonymsAMPA Positive Allosteric Modulator, CX546, CX-546, CX 546
          References
          ReferencesSilverman, L., et al. 2013. Neuropharmacol. 64, 268.
          Peleg-Raibstein, D., et al. 2012. Curr. Antipsych. 2012, 361.
          Schitine, C., et al. 2012. Eur. J. Neurosci. 35, 1672.
          Lipina, T., et al. 2006. Neuropsychopharmacology. 32, 745.
          Arai, C., et al. 2004. Neurosci. 123, 1011.
          Nagarajan, N., et al. 2001. Neuropharmacol. 41, 650.
          Product Information
          CAS number 215923-54-9
          FormOff-white solid
          Hill FormulaC₁₄H₁₇NO₃
          Chemical formulaC₁₄H₁₇NO₃
          Structure formula ImageStructure formula Image
          Applications
          Biological Information
          Primary TargetAMPA
          Purity≥98% by TLC
          Physicochemical Information
          Dimensions
          Materials Information
          Toxicological Information
          Safety Information according to GHS
          Safety Information
          Product Usage Statements
          Storage and Shipping Information
          Ship Code Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
          Toxicity Standard Handling
          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

          CX546 - CAS 215923-54-9 - Calbiochem SDS

          Title

          Safety Data Sheet (SDS) 

          References

          Reference overview
          Silverman, L., et al. 2013. Neuropharmacol. 64, 268.
          Peleg-Raibstein, D., et al. 2012. Curr. Antipsych. 2012, 361.
          Schitine, C., et al. 2012. Eur. J. Neurosci. 35, 1672.
          Lipina, T., et al. 2006. Neuropsychopharmacology. 32, 745.
          Arai, C., et al. 2004. Neurosci. 123, 1011.
          Nagarajan, N., et al. 2001. Neuropharmacol. 41, 650.
          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.

          Revision12-September-2013 JSW
          SynonymsAMPA Positive Allosteric Modulator, CX546, CX-546, CX 546
          DescriptionA positive allosteric modulator selective for the AMPA receptors. Used in studies related to Schizophrenia, neuroplasticity, Autism and neuronal differentiation.
          FormOff-white solid
          CAS number 215923-54-9
          Chemical formulaC₁₄H₁₇NO₃
          Structure formulaStructure formula
          Purity≥98% by TLC
          SolubilityDMSO
          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 Standard Handling
          ReferencesSilverman, L., et al. 2013. Neuropharmacol. 64, 268.
          Peleg-Raibstein, D., et al. 2012. Curr. Antipsych. 2012, 361.
          Schitine, C., et al. 2012. Eur. J. Neurosci. 35, 1672.
          Lipina, T., et al. 2006. Neuropsychopharmacology. 32, 745.
          Arai, C., et al. 2004. Neurosci. 123, 1011.
          Nagarajan, N., et al. 2001. Neuropharmacol. 41, 650.