á741ñMELTING RANGE OR TEMPERATURE
For Pharmacopeial purposes,the melting range or temperature of a solid is defined as those points of temperature within which,or the point at which,the solid coalesces and is completely melted,except as defined otherwise for Classes IIand IIIbelow.Any apparatus or method capable of equal accuracy may be used.The accuracy should be checked at suitable intervals by the use of one or more of the six USP Melting Point Reference Standards,preferably those that melt nearest the melting temperatures of the compounds being tested (see USP Reference Standards á11ñ).
Five procedures for the determination of melting range or temperature are given herein,varying in accordance with the nature of the substance.When no class is designated in the monograph,use the procedure for Class Ia.
The procedure known as the mixed-melting point determination,whereby the melting range of a solid under test is compared with that of an intimate mixture of equal parts of the solid and an authentic specimen of it,e.g.,the corresponding USP Reference Standard,if available,may be used as a confirmatory identification test.Agreement of the observations on the original and the mixture constitutes reliable evidence of chemical identity.

Apparatus I— An example of a suitable melting range Apparatus Iconsists of a glass container for a bath of transparent fluid,a suitable stirring device,an accurate thermometer (see Thermometers á21ñ),*and a controlled source of heat.The bath fluid is selected with a view to the temperature required,but light paraffin is used generally and certain liquid silicones are well adapted to the higher temperature ranges.The fluid is deep enough to permit immersion of the thermometer to its specified immersion depth so that the bulb is still about 2cm above the bottom of the bath.The heat may be supplied by an open flame or electrically.The capillary tube is about 10cm long and 0.8to 1.2mm in internal diameter with walls 0.2to 0.3mm in thickness.

Apparatus II— An instrument may be used in the procedures for Classes I,Ia,and Ib.An example of a suitable melting range Apparatus IIconsists of a block of metal that may be heated at a controlled rate,its temperature being monitored by a sensor.The block accommodates the capillary tube containing the test substance and permits monitoring of the melting process,typically by means of a beam of light and a detector.The detector signal may be processed by a microcomputer to determine and display the melting point or range,or the detector signal may be plotted to allow visual estimation of the melting point or range.

Procedure for Class I,Apparatus I— Reduce the substance under test to a very fine powder,and,unless otherwise directed,render it anhydrous when it contains water of hydration by drying it at the temperature specified in the monograph,or,when the substance contains no water of hydration,dry it over a suitable desiccant for not less than 16hours.
Charge a capillary glass tube,one end of which is sealed,with a sufficient amount of the dry powder to form a column in the bottom of the tube 2.5to 3.5mm high when packed down as closely as possible by moderate tapping on a solid surface.
Heat the bath until the temperature is about 30below the expected melting point.Remove the thermometer,and quickly attach the capillary tube to the thermometer by wetting both with a drop of the liquid of the bath or otherwise,and adjust its height so that the material in the capillary is level with the thermometer bulb.Replace the thermometer,and continue the heating,with constant stirring,sufficiently to cause the temperature to rise at a rate of about 3per minute.When the temperature is about 3below the lower limit of the expected melting range,reduce the heating so that the temperature rises at a rate of about 1to 2per minute.Continue heating until melting is complete.
The temperature at which the column of the substance under test is observed to collapse definitely against the side of the tube at any point is defined as the beginning of melting,and the temperature at which the test substance becomes liquid throughout is defined as the end of melting or the “melting point.”The two temperatures fall within the limits of the melting range.

Procedure for Class Ia,Apparatus I— Prepare the test substance and charge the capillary as directed for Class I,Apparatus I.Heat the bath until the temperature is about 10below the expected melting point and is rising at a rate of 1±0.5per minute.Insert the capillary as directed under Class I,Apparatus Iwhen the temperature is about 5below the lower limit of the expected melting range,and continue heating until melting is complete.Record the melting range as directed for Class I,Apparatus I.

Procedure for Class Ib,Apparatus I— Place the test substance in a closed container and cool to 10,or lower,for at least 2hours.Without previous powdering,charge the cooled material into the capillary tube as directed for Class I,Apparatus I,then immediately place the charged tube in a vacuum desiccator and dry at a pressure not exceeding 20mm of mercury for 3hours.Immediately upon removal from the desiccator,fire-seal the open end of the tube,and as soon as practicable proceed with the determination of the melting range as follows:Heat the bath until a temperature 10±1below the expected melting range is reached,then introduce the charged tube,and heat at a rate of rise of 3±0.5per minute until melting is complete.Record the melting range as directed for Class I,Apparatus I.
If the particle size of the material is too large for the capillary,pre-cool the test substance as above directed,then with as little pressure as possible gently crush the particles to fit the capillary,and immediately charge the tube.

Procedure for Class I,Apparatus II— Prepare the substance under test and charge the capillary tube as directed for Class I,Apparatus I.Operate the apparatus according to the manufacturer's instructions.Heat the block until the temperature is about 30below the expected melting point.Insert the capillary tube into the heating block,and continue heating at a rate of temperature increase of about 1to 2per minute until melting is complete.
The temperature at which the detector signal first leaves its initial value is defined as the beginning of melting,and the temperature at which the detector signal reaches its final value is defined as the end of melting,or the melting point.The two temperatures fall within the limits of the melting range.
In the event of dispute,only the melting range or temperature obtained as directed for Class I,Apparatus I,is definitive.

Procedure for Class II— Carefully melt the material to be tested at as low a temperature as possible,and draw it into a capillary tube,which is left open at both ends,to a depth of about 10mm.Cool the charged tube at 10,or lower,for 24hours,or in contact with ice for at least 2hours.Then attach the tube to the thermometer by suitable means,adjust it in a water bath so that the upper edge of the material is 10mm below the water level,and heat as directed for Class I,Apparatus Iexcept,within 5of the expected melting temperature,to regulate the rate of rise of temperature to 0.5to 1.0per minute.The temperature at which the material is observed to rise in the capillary tube is the melting temperature.

Procedure for Class III— Melt a quantity of the test substance slowly,while stirring,until it reaches a temperature of 90to 92.Remove the source of the heat and allow the molten substance to cool to a temperature of 8to 10above the expected melting point.Chill the bulb of a suitable thermometer (see Thermometers á21ñ)to 5,wipe it dry,and while it is still cold dip it into the molten substance so that approximately the lower half of the bulb is submerged.Withdraw it immediately,and hold it vertically away from the heat until the wax surface dulls,then dip it for 5minutes into a water bath having a temperature not higher than 16.
Fix the thermometer securely in a test tube so that the lower point is 15mm above the bottom of the test tube.Suspend the test tube in a water bath adjusted to about 16,and raise the temperature of the bath at the rate of 2per minute to 30,then change to a rate of 1per minute,and note the temperature at which the first drop of melted substance leaves the thermometer.Repeat the determination twice on a freshly melted portion of the test substance.If the variation of three determinations is less than 1,take the average of the three as the melting point.If the variation of three determinations is 1or greater than 1,make two additional determinations and take the average of the five.
*  ASTM Method E77deals with “Verification and Calibration of Liquid-in-glass Thermometers.”