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Hydrochloric Acid Used in Pharmaceutical Synthesis for API Production

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Product Spotlights

High-purity pharmaceutical grade hydrochloric acid (≥36%) for API synthesis, with certification. Low heavy metals, batch-to-batch consistency, customizable packaging, and global shipping from Tianjin port. Trusted by manufacturers in North America, Europe, and Asia. Support cGMP compliance and improve reaction yield.
US$ 100000 - 2000000 MOQ: 1 Set
Key Specifications
Get Latest Price
Warranty:
2 Years
Voltage:
380V
Application:
Industry
Payment & Shipping
Payment Methods:
Port of Shipment:
Shanghai
Delivery Detail:
Delivery time depends on order quantity.
Warranty 2 Years
Voltage 380V
Application Industry
After-sales Service local technical support
Disinfection Method Chlorine Dioxide
Transport Package Container
Specification Customized
Trademark ZLN
Origin China

As a leading manufacturer of high-purity chemical reagents, Tianjin ZhuoLiNeng (ZLN) Technology Co., Ltd. is proud to offer Pharmaceutical Grade Hydrochloric Acid specifically designed for API (Active Pharmaceutical Ingredient) synthesis. Our hydrochloric acid is produced under strict quality control to ensure consistent purity, low heavy metal content, and minimal impurities, making it an ideal choice for critical pharmaceutical reactions. With certification and a global shipping network from Tianjin port, we deliver reliable chemical solutions to customers across North America, Europe, Asia, and beyond.

Key Features & Technical Specifications

  • High Purity – ≥36% concentration (customizable from 30% to 37%) with extremely low levels of iron, sulfate, and chloride impurities.

  • Pharmaceutical Grade – Meets USP/EP/ACS standards for API synthesis, pH control, and intermediate production.

  • Reliable Supply Chain – Manufactured in our certified facility in Tianjin, ensuring batch-to-batch consistency.

  • Safe Packaging – Available in 25L, 200L, and 1000L IBC drums, with options for custom labeling and inert gas blanketing.

  • Versatile Applications – Used in the synthesis of antibiotics, antivirals, cardiovascular drugs, and other APIs.

  • Traceability – Each batch comes with a Certificate of Analysis (COA) and Material Safety Data Sheet (MSDS).

Parameter Specification
Assay (HCl) 36.0% – 37.0%
Color (APHA) ≤ 10
Residue on Ignition ≤ 0.0005%
Heavy Metals (as Pb) ≤ 0.0005%
Iron (Fe) ≤ 0.0001%
Sulfate (SO₄) ≤ 0.0001%
Arsenic (As) ≤ 0.00001%

Benefits for Your API Production

  • Enhanced Reaction Yield – High purity minimizes side reactions, improving overall API yield.

  • Regulatory Compliance – Our product supports cGMP requirements and helps you meet FDA/EMA standards.

  • Cost Efficiency – Consistent quality reduces batch failure risk and rework costs.

  • Global Logistics – With Tianjin port proximity, we offer fast and flexible shipping options worldwide.

Trusted by Pharmaceutical Manufacturers Worldwide

Tianjin ZLN Technology has been a reliable partner for over a decade, serving customers in North America, South America, Europe, Southeast Asia, Africa, and Oceania. Our  certified facility ensures rigorous quality control, and our dedicated technical team provides comprehensive support for product selection, handling, and compliance. We have successfully supplied hydrochloric acid for the synthesis of multiple critical APIs, including generic and branded drugs. With a strong domestic market presence and a growing international footprint, we are committed to delivering excellence at every step.

Frequently Asked Questions

  1. Q: Is this hydrochloric acid suitable for use in the production of injectable APIs?
    A: Yes, our pharmaceutical grade hydrochloric acid meets high purity standards suitable for injectable API synthesis. However, additional validation for specific applications is recommended.

  2. Q: What is the typical lead time for orders?
    A: For standard packaging (200L drums), lead time is 7–10 working days after order confirmation. Bulk orders may require 15–20 days.

  3. Q: Can you provide a Certificate of Analysis (COA) for each batch?
    A: Absolutely. We supply a detailed COA with every shipment, including assay, impurity profile, and heavy metals analysis.

  4. Q: Do you offer custom packaging or labeling?
    A: Yes, we offer customizable packaging options (e.g., 25L, 1000L IBC) and can provide private label or neutral labeling upon request.

  5. Q: What is the shelf life of your hydrochloric acid?
    A: When stored under recommended conditions (cool, dry, away from alkaline substances), the shelf life is typically 12 months from the date of manufacture.

  6. Q: How do you ensure product consistency across different batches?
    A: Our quality management system includes strict in-process and final product testing using validated methods, ensuring batch-to-batch consistency.

  7. Q: Do you ship samples for evaluation?
    A: Yes, we provide free samples (250mL or 1L) for qualification purposes, with the buyer covering shipping costs.

Contact us today to request a quote, sample, or technical data sheet. Let Tianjin ZLN Technology be your trusted partner for high-quality hydrochloric acid in pharmaceutical synthesis.

Product Tags: Pharmaceutical Grade Hydrochloric Acid , API Synthesis Hydrochloric Acid , High Purity HCl for Drug Manufacturing

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Gold Verified Supplier
1Yr
Verified Business License
Business Type
Manufacturer
Product Certifications
ISO9001, Others
Port of Shipment
TianJin
Main Markets
North America, South America, Eastern Europe, Southeast Asia, Africa, Oceania, Mid East, Eastern Asia, Western Europe, Central America, Northern Europe, Southern Europe, South Asia, Domestic Market