An Analytical Reference Standard
Technical Support & Resources

Visit our FAQ

Contact Us

Toll Free Phone (USA and Canada Only): (888) 526-5351
Direct Phone: (734) 975-3888

Request Technical Support

Technical Support Request

To streamline the process attach the appropriate questionnaire to your inquiry.

Download IHC QuestionnaireDownload WB Questionnaire

View Our Privacy Statement for details on how we use and protect your data. In addition, this site is protected by hCaptcha and its Privacy Policy and Terms of Service apply.

Dibenzyl

Item No. 43544

Synonyms
Synonyms
  • 1,2-Diphenylethane
  • Bibenzyl
Technical Information
Formal Name
1,1′-(1,2-ethanediyl)bis-benzene
CAS Number
103-29-7
Molecular Formula
C14H14
Formula Weight
Purity
≥98%
A solid
DMSO: Sparingly Soluble: 1-10 mg/mL
SMILES
C1(CCC2=CC=CC=C2)=CC=CC=C1
InChi Code
InChI=1S/C14H14/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1-10H,11-12H2
InChi Key
QWUWMCYKGHVNAV-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Certificates of Analysis & Batch Specific Data

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

    Add

    Add

    Cayman Chemical
    Cayman Spectral Library

    Our free, searchable, GC-MS spectral database contains 70eV EI mass spectral data of 2,000+ of Cayman’s forensic drug standards.

    DOWNLOAD THE DATABASE
    Product Description

    Dibenzyl (Item No. 43544) is an analytical reference standard categorized as an aromatic hydrocarbon. Dibenzyl has been found as an impurity in the synthesis of (±)-methamphetamine (Item Nos. ISO60168 | 14216 | 36566).1 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. Kunalan, V., Nic Daéid, N., Kerr, W.J., et al. Characterization of route specific impurities found in methamphetamine synthesized by the Leuckart and reductive amination methods. Anal. Chem. 81(17), 7342-7348 (2009).