Cyclopentolate Hydrochloride

Cyclopentolate Hydrochloride

Cat Number
API5870291
CAS Number
5870-29-1

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CAS Number
5870-29-1
EINECS
227-521-8
Storage
Room temperature
Synonyms
2-(dimethylamino)ethyl1-hydroxy-alpha-phenylcyclopentaneacetatehydrochlorid;alpha-(1-hydroxycyclopentyl)-benzeneaceticaci2-(dimethylamino)ethylest;2Chemicalbook-dimethylaminoethyl2-(1-hydroxycyclopentyl)-2-phenylacetatehydrochloride;2-dimethylaminoethyl2-(1-hydroxycyclopentyl)-2-phenyl-ethanoatehydrochloride
Molecular Formula
C17H26ClNO3
Molecular Weight
327.8
Smiles
CN(C)CCOC(=O)C(C1=CC=CC=C1)C2(CCCC2)O.Cl
Appearance
White to off-white solid
Melting Point
137-141℃
General Description
Cyclopentolate Hydrochloride is a synthetic anticholinergic agent of the tropicamide class. It is specifically developed for ophthalmic use, characterized by rapid onset and a comparatively short duration of mydriatic and cycloplegic action relative to atropine.
Mechanism of Action
Cyclopentolate Hydrochloride competitively blocks muscarinic cholinergic receptors in the iris sphincter and ciliary muscle, preventing acetylcholine binding. This results in relaxation of the iris sphincter muscle (mydriasis) and paralysis of the ciliary muscle (cycloplegia), facilitating ophthalmic examination.
Application
Used in ophthalmology for diagnostic and therapeutic mydriasis and cycloplegia. Cyclopentolate Hydrochloride is a short-acting anticholinergic agent that produces rapid pupillary dilation and ciliary muscle paralysis, facilitating fundus examination, retinoscopy, and measurement of refractive errors.

Cyclopentolate hydrochloride functions as an antimuscarinic (anticholinergic) agent that blocks cholinergic stimulation at muscarinic receptors located on the sphincter muscle of the iris and the accommodative muscle of the ciliary body. This competitive antagonism prevents the responses typically mediated by acetylcholine, resulting in pupillary dilation (mydriasis) and paralysis of accommodation (cycloplegia). The drug acts rapidly after topical ocular instillation, with maximal cycloplegia achieved within 25 to 75 minutes. Complete recovery of accommodation usually requires 6 to 24 hours, while mydriasis may persist for several days in some individuals, particularly those with heavily pigmented irides. Heavily pigmented irides may require more doses or higher concentrations than lightly pigmented irides to achieve the same effect. This mechanism enables comprehensive ophthalmic examinations, including accurate refractive error assessment and thorough fundus evaluation.

Fig. 1 RRS spectra of Cyclopentolate (CYP), erythrosine dye and its reaction product with CYP. (Abu-Hassan A A. 2025) Fig. 1 RRS spectra of Cyclopentolate (CYP), erythrosine dye and its reaction product with CYP. (Abu-Hassan A A. 2025)

References

  1. Abu-Hassan A A. Spectroscopic quantification of cyclopentolate using an erythrosine-based resonance rayleigh scattering strategy: application to ophthalmic formulations. Scientific Reports, 2025, 15(1): 37353.

What distinguishes Cyclopentolate Hydrochloride from tropicamide in ophthalmic practice?

Cyclopentolate Hydrochloride provides more intense and longer-lasting cycloplegia compared to tropicamide, making it the preferred agent for complete ciliary muscle paralysis in pediatric refraction.

What storage conditions are recommended for Cyclopentolate Hydrochloride?

Cyclopentolate Hydrochloride should be stored at room temperature in a sealed container, protected from light and moisture.

What purity grade is available for Cyclopentolate Hydrochloride?

Cyclopentolate Hydrochloride is supplied as a high-purity grade suitable for ophthalmic R&D and pharmaceutical manufacturing.

Can packaging and order quantities be customized?

Yes, custom packaging and labeling options are available to meet diverse laboratory and manufacturing requirements.
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