Bicyclo[2.2.1]heptane-2-one, 1,7,7-trimethyl-.
Camphor.
2-Bornanone
[
76-22-2].
Packaging and storage
Preserve in tight containers, and avoid exposure to excessive heat.
Labeling
Label it to indicate whether it is obtained from natural sources or is prepared synthetically.
Specific rotation 781S:
between +41
and +43
, for natural Camphor.
Test solution:
100 mg per mL, in alcohol.
Synthetic Camphor is optically inactive.
Water
A 1 in 10 solution in solvent hexane is clear.
Limit of nonvolatile residue
Heat 2.0 g in a tared dish on a steam bath until sublimation is complete. Then dry the residue at 120
for 3 hours, cool, and weigh: the weight of the residue does not exceed 1.0 mg (0.05%).
Halogens
Mix 100 mg of finely divided Camphor with 200 mg of sodium peroxide in a clean, dry, hard glass test tube of about 25-mm internal diameter and 20-cm length. Suspend the tube at an angle of about 45
by means of a clamp placed at the upper end, and gently heat the tube, starting near the upper end, but not heating the clamp, and gradually bringing the heat toward the lower part of the tube until incineration is complete. Dissolve the residue in 25 mL of warm water, acidify with nitric acid, and filter the solution into a comparison tube. Wash the test tube and the filter with two 10-mL portions of hot water, adding the washings to the filtered solution. To the filtrate add 0.50 mL of 0.10 N silver nitrate, dilute with water to 50 mL, and mix: the turbidity does not exceed that produced in a blank test with the same quantities of the same reagents and 0.050 mL of 0.020 N hydrochloric acid (0.035%).
Auxiliary Information
Staff Liaison :
Behnam Davani, Ph.D., MBA, Senior Scientist
Expert Committee : (MDAA05) Monograph Development-Antivirals and Antimicrobials
USP29NF24 Page 362
Pharmacopeial Forum : Volume No. 31(3) Page 742
Phone Number : 1-301-816-8394