{"id":20379,"date":"2022-10-21T01:25:24","date_gmt":"2022-10-20T17:25:24","guid":{"rendered":"https:\/\/pharmint.xyz\/?post_type=product&#038;p=20379"},"modified":"2025-08-04T22:38:21","modified_gmt":"2025-08-04T17:08:21","slug":"phenylephrine-hydrochloride","status":"publish","type":"product","link":"https:\/\/pharmint.net\/fr\/product\/phenylephrine-hydrochloride\/","title":{"rendered":"Phenylephrine Hydrochloride"},"content":{"rendered":"<h2 style=\"text-align: center;\"><a href=\"https:\/\/pharmint.net\/product\/phenylephrine-hydrochloride\/\" target=\"_blank\" rel=\"noopener\"><strong>Phenylephrine Hydrochloride (CAS 61-76-7)<\/strong><\/a><\/h2>\n<h4 style=\"text-align: center;\"><strong>Reliable Bulk Supply for Regulated Pharma Markets<\/strong><\/h4>\n<h5><\/h5>\n<h5><strong>What Is Phenylephrine Hydrochloride (CAS 61-76-7) Used For in Pharmaceuticals?<\/strong><\/h5>\n<p>Phenylephrine Hydrochloride is a pharmaceutically active compound classified as a&nbsp;<strong>selective &alpha;&#8321;&#8209;adrenergic receptor agonist<\/strong>, widely recognized for its role in decongestant, vasopressor, and mydriatic formulations. As a hydrochloride salt, it offers enhanced solubility, stability, and formulation compatibility, making it ideal for inclusion in oral tablets, injectable <a href=\"https:\/\/pharmint.net\/fr\/glossary\/ampoule\/\" target=\"_self\" title=\"What is an Ampoule in Pharmaceutical Packaging? An ampoule is a small, hermetically sealed glass container (or sometimes inert plastic) designed to hold a single dose of a sterile liquid, solution, or injectable pharmaceutical product. Once sealed, it is opened by breaking the neck &mdash; ensuring contents are protected from air, moisture, and contaminant exposure.&nbsp;&hellip;\" class=\"encyclopedia\">ampoule<\/a>s, and ophthalmic drops.<\/p>\n<p>In B2B pharmaceutical procurement, Phenylephrine HCl is a critical API sourced for regulated drug formulations, particularly in the production of over-the-counter (OTC) cold and allergy medications, hemodynamic support agents, and eye-care solutions. Its pharmacodynamic precision and long-established safety profile make it a preferred molecule among&nbsp;<strong>generic drug manufacturers<\/strong>,&nbsp;<strong>CMOs<\/strong>, and&nbsp;<strong>hospital pharmacy networks<\/strong>&nbsp;worldwide.<\/p>\n<p>Pharmint offers this API with full documentation support&mdash;COA, MSDS, USP\/EP compliance, and optional DMF\/CEP access&mdash;ensuring smooth onboarding into validation workflows, product registration dossiers, and global supply chains.<\/p>\n<h3><strong>Why Should B2B Buyers Choose Pharmint for Phenylephrine HCl Supply?<\/strong><\/h3>\n<p>Pharmint provides&nbsp;<strong>GMP-compliant, pharmacopeia-grade API<\/strong>&nbsp;with global export readiness, documentation support, and consistent quality assurance&mdash;tailored for CDMOs, CMOs, and pharma manufacturers.<\/p>\n<h3><strong>What Industries and Use Cases Benefit from Bulk Phenylephrine HCl?<\/strong><\/h3>\n<ul>\n<li><strong>OTC Manufacturers<\/strong>: For cold\/cough medicines<\/li>\n<li><strong>API Exporters<\/strong>: With regulatory dossiers for CEP\/DMF<\/li>\n<li><strong>Hospital Buyers<\/strong>: For injectable pressor agents<\/li>\n<li><strong>Ophthalmic Drug Producers<\/strong>: For diagnostic and surgical formulations<\/li>\n<\/ul>\n<h3><strong>What Are the Technical and Compliance Specifications?<\/strong><\/h3>\n<table style=\"width: 449.109px;\">\n<tbody>\n<tr>\n<td style=\"width: 101px;\"><strong>Attribute<\/strong><\/td>\n<td style=\"width: 331.109px;\"><strong>Details<\/strong><\/td>\n<\/tr>\n<tr>\n<td style=\"width: 101px;\">Product Name<\/td>\n<td style=\"width: 331.109px;\">Phenylephrine Hydrochloride<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 101px;\">CAS Number<\/td>\n<td style=\"width: 331.109px;\">61-76-7<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 101px;\">Molecular Formula<\/td>\n<td style=\"width: 331.109px;\">C&#8329;H&#8321;&#8324;ClNO&#8322;<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 101px;\">Molecular Weight<\/td>\n<td style=\"width: 331.109px;\">203.67 g\/mol<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 101px;\">Purity<\/td>\n<td style=\"width: 331.109px;\">&ge;99% (HPLC)<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 101px;\">Appearance<\/td>\n<td style=\"width: 331.109px;\">White to off-white crystalline powder<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 101px;\">Compliance<\/td>\n<td style=\"width: 331.109px;\">USP, EP, GMP<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 101px;\">Packaging<\/td>\n<td style=\"width: 331.109px;\">HDPE drums or custom sterile units<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 101px;\">Shelf Life<\/td>\n<td style=\"width: 331.109px;\">36 months (sealed, refrigerated)<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 101px;\">Documentation<\/td>\n<td style=\"width: 331.109px;\">COA, MSDS, DMF\/CEP available<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h3><strong>How Does Pharmint Ensure Regulatory and Documentation Readiness?<\/strong><\/h3>\n<p>We provide&nbsp;<strong>auditable GMP documentation<\/strong>,&nbsp;<strong>batch COAs<\/strong>, and&nbsp;<strong><a href=\"https:\/\/pharmint.net\/fr\/glossary\/impurity-profile\/\" target=\"_self\" title=\"What Is an Impurity Profile? An&nbsp;impurity profile&nbsp;is a comprehensive characterization of&nbsp;identified and unidentified impurities&nbsp;in a drug substance or pharmaceutical product. According to ICH Q7, this profile should include qualitative or structural identification (like retention time), observed impurity ranges, and classification of impurities (e.g., organic, inorganic, solvent). Why Is Impurity Profiling Critical in Pharmaceuticals? Impurity profiling&hellip;\" class=\"encyclopedia\">impurity profile<\/a>s<\/strong>&nbsp;aligned with ICH Q7 and pharmacopeial monographs. Export licenses and end-use declarations are managed in compliance with country-specific regulations.<\/p>\n<h3><strong>What Are the Supply Chain and Sourcing Advantages?<\/strong><\/h3>\n<ul>\n<li>Bulk inventory for short <a href=\"https:\/\/pharmint.net\/fr\/glossary\/lead-time\/\" target=\"_self\" title=\"What Is Lead Time in Pharmaceutical Operations? Lead Time&nbsp;is the total duration from the initiation of a process (e.g., ordering materials) to its completion (e.g., receiving the finished product). This includes all steps from sourcing&nbsp;raw materials&nbsp;through manufacturing and&nbsp;quality control, to final delivery. Why Is Lead Time Important in Pharma? Operational Planning: Understanding lead times helps&hellip;\" class=\"encyclopedia\">lead time<\/a><\/li>\n<li>Global reach with customs support<\/li>\n<li>Dedicated account managers for strategic sourcing<\/li>\n<li>Support for tech transfer, validation, and dossier filing<\/li>\n<\/ul>\n<h3><strong>How Can I Request Pricing, Samples, or a Regulatory File?<\/strong><\/h3>\n<p>Reach out for a custom quote, batch documentation, or product registration file. We support pilot batch delivery, MOQ flexibility, and long-term supply contracts.<\/p>\n<h2><strong>Phenylephrine HCl FAQs&nbsp;<\/strong><\/h2>\n<h4><strong>What documents are needed to import Phenylephrine HCl for formulation use?<\/strong><\/h4>\n<p>Importers must present COA, MSDS, and often a valid DMF or CEP along with an end-use declaration, as regulated agencies predicate substance control on final formulation intent.<\/p>\n<h4><strong>Can Phenylephrine Hydrochloride be used in combination drug formulations?<\/strong><\/h4>\n<p>Yes, Phenylephrine HCl is commonly formulated with antihistamines or NSAIDs; regulatory authorities predicate combination drug approval on bioequivalence and compatibility studies.<\/p>\n<h4><strong>How is Phenylephrine HCl stability ensured during storage and transit?<\/strong><\/h4>\n<p>Stability is maintained when stored in sealed, light-resistant packaging at 2&ndash;8&#8239;&deg;C; GMP protocols predicate cold-chain logistics on integrity of batch ID and moisture control.<\/p>\n<h4><strong>Does Pharmint provide validation or reference standard support?<\/strong><\/h4>\n<p>Pharmint supplies validation-grade API with HPLC data, <a href=\"https:\/\/pharmint.net\/fr\/glossary\/impurity-profile\/\" target=\"_self\" title=\"What Is an Impurity Profile? An&nbsp;impurity profile&nbsp;is a comprehensive characterization of&nbsp;identified and unidentified impurities&nbsp;in a drug substance or pharmaceutical product. According to ICH Q7, this profile should include qualitative or structural identification (like retention time), observed impurity ranges, and classification of impurities (e.g., organic, inorganic, solvent). Why Is Impurity Profiling Critical in Pharmaceuticals? Impurity profiling&hellip;\" class=\"encyclopedia\">impurity profile<\/a>s, and <a href=\"https:\/\/pharmint.net\/fr\/glossary\/reference-standard\/\" target=\"_self\" title=\"A&nbsp;reference standard&nbsp;(or reference material) is a highly characterized substance used as a benchmark in pharmaceutical analytical testing&mdash;for identity, assay, or purity evaluations. It must be of sufficient quality for its purpose and may undergo additional characterization beyond routine testing.&nbsp; Why is a Reference Standard Critical in Pharmaceutical Analysis? Reference standards are the&nbsp;foundation of analytical consistency&hellip;\" class=\"encyclopedia\">reference standard<\/a>s when requested, supporting predicate analytical method development in QC labs.<\/p>\n<h4><strong>What export restrictions apply to Phenylephrine HCl?<\/strong><\/h4>\n<p>While not universally controlled, exports predicate licensing on country-specific pharmaceutical regulations and may require end-user declarations for customs clearance.<\/p>","protected":false},"excerpt":{"rendered":"<p>Phenylephrine is used for the temporary relief of stuffy nose, sinus, and ear symptoms caused by the common cold, flu, allergies, or other breathing illnesses (such as sinusitis, bronchitis)<\/p>","protected":false},"featured_media":20343,"comment_status":"open","ping_status":"closed","template":"","meta":{"rank_math_lock_modified_date":false,"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","theme-transparent-header-meta":"default","adv-header-id-meta":"","stick-header-meta":"default","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"set","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center 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