Glycine

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Pharmaceutical Grade Glycine (C₂H₅NO₂)
Ultra-Pure Glycine Conforming to USP, EP, BP & FCC Standards for Pharmaceutical, Nutraceutical and Cosmetic Applications.

- ✅ **≥99.5% Purity** (HPLC Verified)
- ✅ **Fully Compliant** with USP-NF, EP, BP, JP & FCC
- ✅ **GMP Manufacturing** | ISO 9001/13485 Certified Facilities
- ✅ **Batch-Specific CoA** with Heavy Metals, Endotoxins & Micro Testing
- ✅ **Customizable**: Particle Size, Packaging (25kg Drums), Logistics
- ✅ **Global Supply**: DDP/DAP Shipping to EU/US/UK
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DetailFAQ 

Pharmaceutical Grade Glycine (USP/EP/BP)

cGMP-Manufactured Amino Acid for Critical Pharma Applications

Key Specifications

  • Purity: ≥99.5% (HPLC)

  • Compliance: USP-NF, EP 10.0, BP 2023

  • Endotoxins: <0.5 EU/mg (Tested by LAL)

Applications in Pharma & Nutraceuticals

Glycine serves as a critical buffer agent in injectable formulations (e.g. IV bags), and as an excipient in orally disintegrating tablets (ODTs)...



Pharmaceutical Grade Glycine (C₂H₅NO₂)

Ultra-Pure Glycine Conforming to USP, EP, BP & FCC Standards for Pharmaceutical, Nutraceutical and Cosmetic Applications.


2. Core selling points

- ✅ **≥99.5% Purity** (HPLC Verified)   

- ✅ **Fully Compliant** with USP-NF, EP, BP, JP & FCC   



3. Detailed technical parameter table

Parameter

Specification (USP/EP Grade)

Test Method

Appearance

White crystalline powder

Visual

Assay (Anhydrous Basis)

98.5–101.5%

USP Titrimetry

pH (1% Solution)

5.5–6.5

USP <791>

Heavy Metals (as Pb)

≤10 ppm

USP <231> / EP 2.4.8

Endotoxins

≤0.5 EU/mg (for Injectable)

USP <85>

Residual Solvents

Complies with ICH Q3C

GC

Microbial Limits

TAMC ≤1000 CFU/g, TYMC ≤100 CFU/g

USP <61>



4. Application Scenarios:

**Injectable Formulations**: Buffer agent in IV solutions.

- **Oral Solid Dosage**: Excipient for tablets/capsules (USP/EP compliant).

- **Sports Nutrition**: Key ingredient in protein supplements (FCC grade).

- **Cosmeceuticals**: Moisturizer & pH stabilizer in anti-aging creams.



Documentation

5.certifications Section

*"Manufactured in cGMP-compliant facilities (ISO 13485:2016). All batches undergo rigorous QA/QC testing."*

��Download Sample CoA | �� Request SDS | �� Full Product Dossier




Compliance & Support

GMP, ISO, HALAL, KOSHER, FDA Registered.

Full technical dossiers (MSDS, TDS, COA, Allergen Statement) are available for every batch.