| Common name | L-Glutamine |
| Synonyms | Gln; Q; 2-Aminoglutaramic acid; Glutamine |
| CAS number | 56-85-9 |
| Molecular formula | C₅H₁₀N₂O₃ |
| Molecular weight | 146.15 g/mol |
| Appearance | White crystalline powder, odourless, tasteless |
| Assay (pharma grade) | ≥99.0% (HPLC, USP/BP) |
| Assay (food grade) | ≥98.5% (HPLC) |
| Specific rotation | [α]D²⁰ = +6.1° to +6.7° (c=2, 6N HCl) |
| pH (5% aqueous solution) | 5.0–6.5 |
| Melting point | 185°C (decomposes) |
| Solubility in water | 3.6 g/100 mL at 20°C; insoluble in ethanol |
| Loss on drying | NMT 0.5% |
| Residue on ignition | NMT 0.1% |
| Heavy metals (total) | NMT 10 ppm |
| Lead | NMT 0.5 ppm |
| Arsenic | NMT 0.5 ppm |
| Microbial limits | TPC NMT 10³ CFU/g; absence of Salmonella, E. coli |
| Source / production | Bacterial fermentation (Corynebacterium glutamicum); non-animal |
| Shelf life | 24 months (<25°C, dry, sealed, away from moisture) |
Every batch tested by HPLC for ≥99% assay, specific rotation, heavy metals, microbial limits, and residual solvents. GMP-certified fermentation source with full traceability documentation.
Assay ≥99.0% (pharma) / ≥98.5% (food) by HPLC. Specific rotation [α]D²⁰ = +6.1° to +6.7° confirms L-isomer identity. Residual solvents and related amino acid impurities profiled per USP.
Bacterial fermentation (Corynebacterium glutamicum). Non-animal, non-GMO certification available. Fermentation batch records provided. No risk of TSE/BSE contamination from animal-derived sources.
TPC NMT 10³ CFU/g; absence of Salmonella, E. coli, Staphylococcus aureus. Lead NMT 0.5 ppm; Arsenic NMT 0.5 ppm; Mercury NMT 0.1 ppm. All tested per USP/EP methods.
Full COA, MSDS, Certificate of Origin. USP/BP analytical certificates. FSSAI compliance for food applications. Halal/Kosher certificates on request. Digital documentation before shipment.
L-Glutamine is simultaneously a clinical nutrition staple (mandated in ICU parenteral protocols) and the world's top-selling sports supplement amino acid. Understanding the grade, application, and formulation stability requirements prevents costly specification errors.
Specified for parenteral nutrition, medical foods and research formulations. Tighter limits on heavy metals (Pb NMT 0.5 ppm), endotoxins, residual solvents. Full USP/BP COA with each batch. Fermentation-derived. Compliant with ESPEN and ASPEN clinical nutrition guidelines.
Suitable for sports recovery supplements, pre/post-workout formulas, general health supplements, and food fortification. Same fermentation source, slightly relaxed analytical limits. Correct specification for the vast majority of commercial supplement applications. Significantly lower cost than pharma grade.
ICU/clinical: 0.2–0.4 g/kg/day IV glutamine (ESPEN guideline). Sports recovery: 5–10g post-exercise. Gut health: 5–15g/day orally. Both are well-supported by clinical evidence. The two segments differ in grade, documentation and specification, so confirm which your finished product is written against.
Glutamine hydrolyses to glutamic acid in aqueous solution, especially at acidic pH and elevated temperature. For powders: moisture barrier packaging, desiccants, NMT 0.5% moisture at manufacture. For ready-to-drink beverages: specify alanyl-L-glutamine dipeptide (Ala-Gln) which is water-stable. Do not blend with reactive reducing sugars in hot processing.
Supplied as a bulk ingredient for further manufacture. Buyers are responsible for compliance with the regulations of their destination market. This product is not intended to diagnose, treat, cure or prevent any disease.
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