NF COMPENDIA |
||||
---|---|---|---|---|
ANALYSIS |
SPECIFICATIONS |
|||
|
398.0% – 102.0% | |||
|
≤ 0.0125% | |||
|
A720 ≤ 0.050 A420 – A720 ≤ 0.100 |
|||
|
3≤ 2.4 EU/g | |||
|
Conforms to standard | |||
|
Passes Test | |||
|
Passes Test | |||
|
Absent/g Absent/10g ≤ 100 CFU/g ≤ 100 CFU/g |
|||
|
≤ 0.005% | |||
2Optical Rotation, Specific Rotation @ 20°C | +197° to +201° | |||
|
4.5 – 6.5 | |||
|
≤ 0.5% |
|||
|
≤ 0.1% | |||
|
Passes Test | |||
|
≤ 0.0200% | |||
|
9.0 – 11.0% |
EP COMPENDIA |
||||
---|---|---|---|---|
ANALYSIS |
SPECIFICATIONS |
|||
|
398.0% – 102.0% | |||
|
Clear, colorless | |||
|
≤ 0.0125% | |||
|
3≤ 2.4 EU/g | |||
|
Conforms to Standard | |||
|
Passes Test | |||
|
Passes Test | |||
|
≤ 0.5% ≤ 0.2% ≤ 1.0% |
|||
|
Absent/g Absent/10g ≤ 100 CFU/g ≤ 100 CFU/g |
|||
|
4.5 – 6.5 | |||
|
Passes Test | |||
|
+197º to +201º | |||
|
≤ 0.1% | |||
|
≤ 0.0200% | |||
|
9.0% to 11.0% |
CP COMPENDIA |
||||
---|---|---|---|---|
ANALYSIS |
SPECIFICATIONS |
|||
|
4.5 – 6.5 | |||
|
98.0 – 102.0% | |||
|
A720 ≤ 0.033 A420 – A720 ≤ 0.067 |
|||
|
≤ 0.0125% | |||
|
3≤ 2.4 EU/g | |||
|
≤ 0.0005% | |||
|
Passes Test | |||
|
Passes Test | |||
|
Passes Test | |||
|
Conforms to Standard | |||
|
Absent/g Absent/10g 3≤ 100 CFU/g ≤ 100 CFU/g |
|||
|
≤ 0.5% ≤ 0.5% |
|||
|
≤ 0.1% | |||
|
Passes Test | |||
|
+197º to +201º | |||
|
≤0.020% | |||
|
9.0 – 11.0% |
NON-COMPENDIAL ANALYSIS |
|||
---|---|---|---|
ANALYSIS |
SPECIFICATIONS |
||
Appearance and Color | White to Almost White Crystalline Powder | ||
|
≤ 5000 ppm | ||
1 Residual Methanol | ≤ 3000 ppm |
1 Alternate Validated Method 2 Analyses are Harmonized
3Specification is more stringent than Compendia Monograph
Bio Excipient Grade Trehalose Dihydrate TRED-3251 is suitable for use as an excipient. It is manufactured in accordance with the ICH-Q7 Good Manufacturing Practice Guide. This grade of Trehalose Dihydrate is not suitable to be used as an Active Pharmaceutical Ingredient, Drug Product or Household Item.
The recommended retest period for Trehalose, Dihydrate TRED-3251 is based on current available stability data in accordance with the Stability Testing Program.
10kg and 25kg pails.
American Manufactured - FDA Registered GMP Facilities: Parenteral Excipients, GMP Small Molecule Intermediates, GMP Biological Buffers, Parenteral Carbohydrates, GMP Chlorinated Amino Acids, GMP Solutions in Sterile Single Use Packaging and other Reagent & GMP Fine Chemicals.