A Certified Reference Material
Features
  • This product is qualified as a Certified Reference Material (CRM) that has been manufactured and tested to meet ISO/IEC 17025 and ISO 17034 international standards
  • This CRM has been characterized by metrologically valid procedures and may be used as a quantitative analytical reference standard
  • Certificate of analysis provides the certified property values and the associated uncertainties, including a statement of metrological traceability for the certified values
  • Bulk material is available for qualified institutions; please contact our sales department for pricing
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Ritalinic Acid (hydrochloride) (CRM)

A 1 mg/ml solution in methanol

Item No. 40261

Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
α-phenyl-2-piperidineacetic acid, monohydrochloride
CAS Number
19395-40-5
Molecular Formula
C13H17NO2 • HCl
Formula Weight
255.7
Formulation
A 1 mg/ml solution in methanol
SMILES
OC(C(C1=CC=CC=C1)C2CCCCN2)=O.Cl
InChi Code
InChI=1S/C13H17NO2.ClH/c15-13(16)12(10-6-2-1-3-7-10)11-8-4-5-9-14-11;/h1-3,6-7,11-12,14H,4-5,8-9H2,(H,15,16);1H
InChi Key
SCUMDQFFZZGUQY-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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Certificates of Analysis & Batch Specific Data

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    1 mg

    $164

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    Product Description

    Ritalinic Acid (hydrochloride) (CRM) (Item No. 40261) is a certified reference material categorized as an amphetamine metabolite.1 Ritalinic acid is a metabolite of (±)-threo-methylphenidate (Item Nos. 40186 | 11639).1 It is also a potential metabolite of (±)-threo-ethylphenidate (Item No. 13896), (±)-threo-isopropylphenidate (Item No. 19264), and (±)-threo-propylphenidate (Item No. 19268) based on the published metabolism of (±)-threo-methylphenidate. This product is intended for research and forensic applications.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Sun, Z., Murry, D.J., Sanghani, S.P., et al. Methylphenidate is stereoselectively hydrolyzed by human carboxylesterase CES1A1. J. Pharmacol. Exp. Ther. 310(2), 469-476 (2004).