D-(-)-Mannitol 97.0-102.0% (dry basis), powder USP, Multi-Compendial GMP Manufactured Product, J.T.Baker®
Supplier: Avantor
Synonyms:
Mannitol, (2R,3R,4R,5R)-Hexane-1,2,3,4,5,6-hexaol
Management of Change (MOC) category = R
2553-01EA
19419.12
INR
2553-01
2553-05
2553-07
2553-09
2553-08
2553-71
2553-75
2553-77
2553-78
D-(-)-Mannitol 97.0-102.0% (dry basis), powder USP, Multi-Compendial GMP Manufactured Product, J.T.Baker®
D(-)-Mannitol
Formula:
HOH₂C(CH(OH))₄CH₂OH MW: 182,17 g/mol Boiling Pt: 290…295 °C (4 hPa) Melting Pt: 164…169 °C Density: 1,52 g/cm³ Storage Temperature: Ambient |
MDL Number:
MFCD00064287 CAS Number: 69-65-8 EINECS: 200-711-8 Merck Index: 13,05769 |
Specification Test Results
GMP Manufactured Product | 97.0 - 102.0% |
Meets E.P. Chemical Specifications | Passes Test |
Meets U.S.P Requirements | ≤2.0% |
Meets B.P. Chemical Specifications | ≤2.0% |
Meets J.P. Chemical Specifications | ≤0.10% |
CAUTION: For Manufacturing, processing or repackaging | ≤2.0% |
Bulk Pharmaceutical Chemical | ≤0.5% |
USP - Assay (dried basis) | 97.0 - 102.0 % |
USP - Identification | Passes Test |
USP - Related Substances: Sorbitol | ≤ 2.0 % |
USP - Related Substances: Sum of isomalt& maltitol | ≤ 2.0 % |
USP - Related Substances: Unspecified impurities | ≤ 0.10 % |
USP - Related Substances: Total impurities | ≤ 2.0 % |
USP - Loss on Drying at 105°C | ≤ 0.5 % |
USP - Melting Point | 165 - 170 °C |
USP - Reducing Sugars | ≤ 0.1 % |
USP - Nickel (Ni) | ≤ 1 ppm |
USP - Appearance of Solution | Passes Test |
USP - Conductivity (uS cm-1) | ≤ 20 µS/cm |
USP - Total Aerobic Microbial Count | ≤ 100 cfu/g |
USP - Total Yeast and Mold Count | ≤ 100 cfu/g |
USP - Escherichia coli | Passes Test |
USP - Bacterial Endotoxins, IU/g | ≤ 2.5 |
EP/BP - Assay (as HOCH₂(CHOH)₄CH₂OH) (dried basis) | 97.0 - 102.0 % |
EP/BP - Identification C | Passes Test |
EP/BP - Melting Point | 165 - 170 °C |
EP/BP - Appearance of Solution | Passes Test |
EP/BP - Conductivity, uS cm-1 | ≤ 20 |
EP/BP - Reducing Sugars | ≤ 0.1 % |
EP/BP - Related Substances: Impurity A | ≤ 2.0 % |
EP/BP - Related Substances: Sum of Impurities B & C | ≤ 2.0 % |
EP/BP - Related Substances: Unspecified Impurities, each | ≤ 0.10 % |
EP/BP - Related Substances: Total Impurities | ≤ 2.0 % |
EP/BP - Loss on Drying | ≤ 0.5 % |
EP/BP - Escherichia coli | None Detected |
EP/BP - Salmonella | None Detected |
EP/BP - Total Yeast and Mold Count | ≤ 100 cfu/g |
EP/BP - Total Aerobic Microbial Count | ≤ 100 cfu/g |
EP/BP Endotoxin Concentration, <2.5 IU/g | Passes Test |
JP - Assay (dried basis) | 97.0 - 102.0 % |
JP - Identification | Passes Test |
JP - Related Substances: Sorbitol | ≤ 2.0 % |
JP - Related Substances: Sum of isomalt & maltitol | ≤ 2.0 % |
JP - Related Substances: Unspecified impurities | ≤ 0.10 % |
JP - Related Substances: Total impurities | ≤ 2.0 % |
JP - Heavy Metals (as Pb) | ≤ 5 ppm |
JP - Loss on Drying at 105°C | ≤ 0.5 % |
JP - Melting Point | 165 - 170 °C |
JP - Glucose | ≤ 0.1 % |
JP - Nickel (Ni) | ≤ 1 ppm |
JP - Clarity and Color of Solution | Passes Test |
JP - Conductivity (uS cm-1) | ≤ 20 µS/cm |
Suitable for use in the manufacture of parenteral dosage forms. | |
Maximum Endotoxin Concentration: 2.5 IU/g | |
No Class 1,2,3 or other solvents are used or produced in the manufacturing or purification of the product. | |
Elemental Impurities (USP 232, EP 5.20) - Information on elemental impurities for this product is available on the associated Product Regulatory Data Sheet and elemental impurity profile report. |
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