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Pilocarpine (CAS 92-13-7)

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Alternate Names:
Spersacarpine; Syncarpine
CAS Number:
92-13-7
Molecular Weight:
208.26
Molecular Formula:
C11H16N2O2
Supplemental Information:
This is as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Pilocarpine is an alkaloid compound that has garnered attention in the field of biochemistry, particularly for its ability to bind and activate muscarinic acetylcholine receptors. In research applications outside of clinical settings, Pilocarpine is often utilized to study the pharmacology of cholinergic neurotransmission, as well as the physiological responses to muscarinic receptor activation. Investigations may examine the impact of Pilocarpine on secretory functions in exocrine tissues or its effects on smooth muscle contraction in vitro. The compound is also used in research models to induce responses that mimic those of the parasympathetic nervous system, which aids in understanding the underlying mechanisms of neurotransmitter action. Additionally, Pilocarpine may serve as a tool compound in the development of receptor agonists or antagonists by providing a reference point for the design of molecules with similar or opposing activities.


Pilocarpine (CAS 92-13-7) References

  1. Sites of reaction of pilocarpine.  |  Satterfield, M. and Brodbelt, JS. 1999. J Am Soc Mass Spectrom. 10: 209-16. PMID: 10069045
  2. Subnanogram assay for pilocarpine in biological fluids.  |  Bayne, WF., et al. 1976. J Pharm Sci. 65: 1724-8. PMID: 1032652
  3. Pump infusion of pilocarpine.  |  Harris, LS. and Kahanowicz, Y. 1975. Ophthalmologica. 171: 157-64. PMID: 1153174
  4. Pilocarpine dispensation for the soft hydrophilic contact lens.  |  Ruben, M. and Watkins, R. 1975. Br J Ophthalmol. 59: 455-8. PMID: 1203231
  5. Simultaneous determination of pilocarpine and isopilocarpine in pharmaceutical preparations by liquid chromatography.  |  Urbányi, T., et al. 1976. J Pharm Sci. 65: 257-60. PMID: 1255459
  6. Salivary flow induction by buccal permucosal pilocarpine in anesthetized beagle dogs.  |  Weaver, ML., et al. 1992. J Dent Res. 71: 1762-7. PMID: 1401437
  7. Unraveling the biosynthesis of pilocarpine in Pilocarpus microphyllus.  |  Sawaya, AC., et al. 2015. Nat Prod Commun. 10: 721-4. PMID: 26058143
  8. Compliance with topical pilocarpine treatment.  |  Kass, MA., et al. 1986. Am J Ophthalmol. 101: 515-23. PMID: 3706455
  9. Pilocarpine used to stimulate normal saliva production.  |  . 1985. J Am Dent Assoc. 111: 310. PMID: 3862698
  10. Pilocarpine prodrugs I. Synthesis, physicochemical properties and kinetics of lactonization of pilocarpic acid esters.  |  Bundgaard, H., et al. 1986. J Pharm Sci. 75: 36-43. PMID: 3958903
  11. Corneal metabolism of pilocarpine in pigmented rabbits.  |  Lee, VH., et al. 1980. Invest Ophthalmol Vis Sci. 19: 210-3. PMID: 7351355
  12. Pilocarpine incorporated into a submicron emulsion vehicle causes an unexpectedly prolonged ocular hypotensive effect in rabbits.  |  Naveh, N., et al. 1994. J Ocul Pharmacol. 10: 509-20. PMID: 7836859
  13. Effect of pilocarpine on anterior chamber angles.  |  Hung, L., et al. 1995. J Ocul Pharmacol Ther. 11: 221-6. PMID: 8590253
  14. Pilocarpine ocular inserts.  |  Bensinger, R., et al. 1976. Invest Ophthalmol. 15: 1008-10. PMID: 992960

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Pilocarpine, 100 mg

sc-479256
100 mg
$255.00