An intermediate product of both the mevalonic acid pathway and the DOXP/MEP pathway
Technical Support & Resources

Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

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.

Product Categories

DMAPP (ammonium salt)

Item No. 63180

Technical Information
Formal Name
3-methyl-2-butenyl-1-diphosphoric acid, triammonium salt
CAS Number
1186-30-7
Synonyms
  • Dimethylallyl Pyrophosphate
Molecular Formula
C5H12O7P2 • 3(NH4)
Formula Weight
A crystalline solid
Methanol: 10mM NH4OH (7:3): 2 mg/mlWater: 25 mg/ml
SMILES
[O-]P([O-])(OP([O-])(OC/C=C(C)\C)=O)=O.[NH4+].[NH4+].[NH4+]
InChi Code
InChI=1S/C5H12O7P2.3H3N/c1-5(2)3-4-11-14(9,10)12-13(6,7)8;;;/h3H,4H2,1-2H3,(H,9,10)(H2,6,7,8);3*1H3
InChi Key
VBUNGGIXIOHBHL-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Recommended Products

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

    Add

    Add

    Lipid Resource Center
    Discover Products & Resources for Lipid Research
    • High-purity lipid standards
    • Lipid roles in biology
    • Lipids in health & disease
    • Lipids for pharmaceutical development
    • Protocols, advice, & resources
    EXPLORE NOW
    Product Description

    Dimethylallyl pyrophosphate and isopentyl pyrophosphate undergo condensation to yield geranyl pyrophosphate, which undergoes condensation with a second molecule of isopentyl pyrophosphate to yield farnesyl pyrophosphate.1,2 Farnesylation is essential for the function of a number of proteins involved in signal transduction.3,4

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Barnard, G.F., and Popják, G. Human liver prenyltransferase and its characterization. Biochim. Biophys. Acta 661, 87-99 (1981).

    2. Laskovics, F.M., and Poulter, C.D. Prenyltransferase: Determination of the binding mechanism and individual kinetic constants for farnesylpyrophosphate synthetase by rapid quench and isotope partitioning experiments. Biochemistry 20, 1893-1901 (1981).

    3. Hohl, R.J., Lewis, K.A., Cermak, D.M., et alStereochemistry-dependent inhibition of Ras farnesylation by farnesylphosphonic acids. Lipids 33, 39-46 (1998).

    4. Rando, R.R. Chemical biology of protein isoprenylation/methylation. Biochim. Biophys. Acta 1300, 5-16 (1996).