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 221 GBP
2553-01 2553-05 2553-07 2553-09 2553-32 2553-34 2553-37 2553-39 2553-38
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
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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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