Change to read:
Labeling—
Where the labeling indicates the relative quantities of alpha and beta lactose, determine compliance using
Content of alpha and beta anomers.
Where the labeling states the particle size distribution, it also indicates the d
10, d
50, and d
90 values and the range for each.
NF26
Add the following:
Clarity and color of solution—
A solution of 1 g in 10 mL of boiling water is clear and nearly colorless. Determine the absorbance of this solution at a wavelength of 400 nm. The absorbance divided by the path length, in cm, is not more than 0.04.
NF26
Add the following:
Specific rotation 
781
—
Dissolve 10 g by heating in 80 mL of water to 50
. Allow to cool, and add 0.2 mL of 6 N ammonium hydroxide. Allow to stand for 30 minutes, and dilute with water to 100 mL: the specific rotation, calculated on the anhydrous basis, determined at 20
, is between +54.4
and +55.9
.
NF26
Add the following:
Microbial limits 61—
The total aerobic microbial count does not exceed 100 cfu per g, the total combined molds and yeasts count does not exceed 50 cfu per g, and it meets the requirements of the test for absence of
Escherichia coli.
NF26
Add the following:
Acidity or alkalinity—
Dissolve 6 g by heating in 25 mL of carbon dioxide-free water, cool, and add 0.3 mL of phenolphthalein TS: the solution is colorless, and not more than 0.4 mL of 0.1 N sodium hydroxide is required to produce a red color.
NF26
Content of alpha and beta anomers—
Silylation reagent—
Prepare a mixture of pyridine and trimethylsilylimidazole (72:28).
Resolution mixture—
Prepare a mixture of alpha lactose monohydrate and beta lactose having an anomeric ratio of about 1:1 based on the labeled anomeric contents of the alpha lactose monohydrate and the beta lactose.
Chromatographic system
(see
Chromatography 621)—The gas chromatograph is equipped with a flame-ionization detector and a 4-mm × 0.9-m glass column packed with 3% liquid phase G19 on support S1A. The column temperature is maintained at about 215
, and the injection port and the detector temperatures are maintained at about 275
. The carrier gas is helium, flowing at a rate of about 40 mL per minute.
Derivatization procedure—
Transfer about 1 mg of Anhydrous Lactose to a 5-mL reaction vial equipped with a screw cap, add 0.45 mL of dimethyl sulfoxide, seal the vial tightly with a screw cap, and mix on a vortex mixer to dissolve. Add 1.8 mL of Silylation reagent, seal the vial tightly with a screw cap, and mix gently. Transfer about 1 mg of Resolution mixture to a second 5-mL reaction vial equipped with a screw cap, add 0.45 mL of dimethyl sulfoxide, seal the vial tightly with a screw cap, and mix on a vortex mixer to dissolve. Add 1.8 mL of Silylation reagent, seal the vial tightly with a screw cap, and mix gently. Maintain both vials at room temperature for 20 minutes before using.
Procedure—
Inject a 2.0-µL portion of the derivatized
Resolution mixture into the chromatograph, and record the peak areas for the major peaks: the relative retention times are about 0.7 for the silyl derivative of alpha lactose and 1.0 for the silyl derivative of beta lactose, and the resolution,
R, between the two peaks is not less than 3.0. Similarly inject a 2.0-µL portion of the derivatized Anhydrous Lactose into the chromatograph, and record the peak areas for the major peaks. Determine the percentage of alpha anomer in the Anhydrous Lactose by the formula:
100ra / (ra + rb)
in which
ra is the response of the alpha anomer silyl derivative peak and
rb is the response of the beta anomer silyl derivative peak. Determine the percentage of beta anomer in the Anhydrous Lactose by the formula:
100rb / (ra + rb)
in which the terms are as defined above.
;)
-d-galactopyranosyl-(1®4)-
-d-glucopyranose (;)
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