Customization: | Available |
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Function: | Pharmaceutical Medicine |
Certification: | GMP, FDA, ISO |
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Audited by an independent third-party inspection agency
Items | Standards | Results |
Appearance | White to off-white powder | Complies |
Identification | By IR | Complies |
By HPLC | Complies | |
Solubility | Slightly soluble in Ethyl Acetate and Acetonitrile and very slightly soluble in Water. | Complies |
Water Content | ≤ 1.00% | 0.37% |
Heavy Metals | ≤ 20ppm | Complies |
Residue on Ignition | ≤ 1.00% | 0.48% |
Residual Solvents | Ethanol: ≤5000ppm | ND |
Dichloromethane ≤600ppm | ND | |
Pyridine: ≤200ppm | ND | |
Triethylamine: ≤320ppm | ND | |
Isopropyl Acetate: ≤5000ppm | ND | |
Methanol: ≤3000ppm | ND | |
Isopropanol: ≤5000ppm | 500ppm | |
Dimethyl sulfoxide: ≤5000ppm | ND | |
Related Substances | Individual Impurity: ≤0.10% | 0.01% |
Total Impurities: ≤1.00% | 0.02% | |
Enantiomer Purity | ≤ 0.10% | 0.01% |
L-Pyroglutamic Acid Assay | 22.1%~24.5% (As C5H7NO3, calculated on anhydrous basis) |
24.6% |
Assay | 98.0%~102.0% (As C22H25ClO7, calculated on anhydrous basis) |
99.98% |
Reference Standard | In-house Standard | |
Conclusion | The product complied to In-house standard. | |
Storage | Preserve in tight,light-resistant containers in a cool place |