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4 Test method
4.
Some test procedures specified by the test method may lead to dangerous situations
4.
Unless otherwise specified, only reagents confirmed to be analytically pure and grade 3 water specified in GB/T6682-1992 are used in the analysis
4.
Visual inspection
4.
4.
Electrode: E-201-C composite electrode
4.
Ferric chloride solution: 25g/L
4.
Take about 40mg of laboratory samples, add 2mL of water to dissolve, add 1 drop of ferric chloride solution, there should be a blue precipitate (an instantaneous turn into a brown precipitate)
4.
4.
4.
Using glacial acetic acid as the solvent, titrate with perchloric acid standard titration solution, determine the titration end point by measuring the electrode potential , and calculate the content of L-p-hydroxyphenylglycine Deng potassium salt in the sample according to the volume of the perchloric acid standard titration solution
.
4.
5.
1.
2 Reagents
4.
5.
1.
2.
1 Glacial acetic acid
.
4.
5.
1.
2.
2 Perchloric acid standard titration solution: c(HC1O 4 )=0.
1mol/L
.
4.
5.
1.
3 Analysis steps
Weigh about 0.
3g laboratory sample, accurate to 0.
0001g
.
Place in a dry 150mL beaker, add 50mL of glacial acetic acid to dissolve, and titrate with perchloric acid standard titration solution to the end point
.
The determination of the volume of perchloric acid standard titration solution adopts the GB/T 9725-1988 6.
2.
2 secondary derivative method
.
4.
5.
1.
4 Result calculation
The mass fraction w 1 of the content of L-p-hydroxyphenylglycine Deng potassium salt , the value is expressed in %, calculated according to formula (1):
Where:
V—The value of the volume of the sample consumption perchloric acid standard titration solution (4.
5.
1.
2.
2), in milliliter (mL);
c—The exact value of the concentration of perchloric acid standard titration solution, the unit is moles per liter (mol/L);
m—The value of the mass of the sample, in grams (g);
M—The value of the molar mass of L-p-hydroxyphenylglycine Deng potassium salt, in grams per mole (g/mol)
Take the arithmetic mean of the two parallel determination results as the determination result, and the absolute difference between the two parallel determination results shall not exceed 0.
3%
.