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505024 Ibotenic Acid - CAS 2552-55-8 - Calbiochem

Overview

Replacement Information

Key Specifications Table

CAS #Empirical Formula
2552-55-8C₅H₆N₂O₄

Pricing & Availability

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5.05024.0001
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      Glass bottle 1 mg
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      Description
      OverviewA highly potent agonist of NMDA and mGlu receptors. A frequently used brain-lesioning agent inducing excitotoxic lesions of neurons without damaging crossing fiber tracts.
      Catalogue Number505024
      Brand Family Calbiochem®
      Synonyms2-amino-2-(3-hydroxyisoxazol-5-yl) acetic acid, α-Amino-(3-hydroxy-5-isoxazolyl)acet­ic acid, Glutamate Receptor Agonist, Ibotenic acid
      References
      ReferencesIzquierdo, A., et al. 2013. J. Neurosci. 33, 4105.
      Rhodes, V., et al. 2013. J. Neurosci. 33, 3380.
      Yu, X., et al. 2012. Pharmacol. Biochem. & Beh. 101, 479.
      Albasser, M., et al. 2012. Beh. Neurosci. 126, 659.
      Eijkenboom, M., et al. 2000. Neurosci. 101, 27.
      Isacson, O., et al. 1984. Nature. 311, 458.
      Product Information
      CAS number2552-55-8
      FormWhite solid
      Hill FormulaC₅H₆N₂O₄
      Chemical formulaC₅H₆N₂O₄
      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
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
      Toxicity Regulatory Review
      Hazardous Materials Attention: Due to the nature of the Hazardous Materials in this shipment, additional shipping charges may be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.
      Storage -20°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
      Global Trade Item Number
      Catalog Number GTIN
      5.05024.0001 04055977263329

      Documentation

      Ibotenic Acid - CAS 2552-55-8 - Calbiochem SDS

      Title

      Safety Data Sheet (SDS) 

      Ibotenic Acid - CAS 2552-55-8 - Calbiochem Certificates of Analysis

      TitleLot Number
      505024

      References

      Reference overview
      Izquierdo, A., et al. 2013. J. Neurosci. 33, 4105.
      Rhodes, V., et al. 2013. J. Neurosci. 33, 3380.
      Yu, X., et al. 2012. Pharmacol. Biochem. & Beh. 101, 479.
      Albasser, M., et al. 2012. Beh. Neurosci. 126, 659.
      Eijkenboom, M., et al. 2000. Neurosci. 101, 27.
      Isacson, O., et al. 1984. Nature. 311, 458.
      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.

      Revision17-July-2013 JSW
      Synonyms2-amino-2-(3-hydroxyisoxazol-5-yl) acetic acid, α-Amino-(3-hydroxy-5-isoxazolyl)acet­ic acid, Glutamate Receptor Agonist, Ibotenic acid
      DescriptionA highly potent agonist of NMDA and mGlu receptors. A frequently used brain-lesioning agent inducing excitotoxic lesions of neurons without damaging crossing fiber tracts.
      FormWhite solid
      CAS number2552-55-8
      Chemical formulaC₅H₆N₂O₄
      Structure formulaStructure formula
      Purity≥99% by HPLC
      SolubilityH₂O (10 mM)
      Storage Protect from light
      -20°C
      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 Regulatory Review
      ReferencesIzquierdo, A., et al. 2013. J. Neurosci. 33, 4105.
      Rhodes, V., et al. 2013. J. Neurosci. 33, 3380.
      Yu, X., et al. 2012. Pharmacol. Biochem. & Beh. 101, 479.
      Albasser, M., et al. 2012. Beh. Neurosci. 126, 659.
      Eijkenboom, M., et al. 2000. Neurosci. 101, 27.
      Isacson, O., et al. 1984. Nature. 311, 458.