PY3205 PHARMACEUTICAL ORGANIC CHEMISTRY LABORATORY SYLLABUS | ANNA UNIVERSITY B.TECH PHARMACEUTICAL TECHNOLOGY 3RD SEMESTER SYLLABUS REGULATION 2008 2011-2012 BELOW IS THE ANNA UNIVERSITY THIRD SEMESTER B.TECH PHARMACEUTICAL TECHNOLOGY DEPARTMENT SYLLABUS IT IS APPLICABLE FOR ALL STUDENTS ADMITTED IN THE YEAR 2011-2012 (ANNA UNIVERSITY CHENNAI,TRICHY,MADURAI,TIRUNELVELI,COIMBATORE), 2008 REGULATION OF ANNA UNIVERSITY CHENNAI AND STUDENTS ADMITTED IN ANNA UNIVERSITY CHENNAI DURING 2009
PY3205 PHARMACEUTICAL ORGANIC CHEMISTRY LABORATORY
1. Determination of Impurities
2. Synthesis of some organic compounds involving single step reactions like
nitration, halogenation, acetylation and hydrolysis.
3. Synthesis of organic compounds involving Two steps
4. Assay of organic compounds involving acidimetry, alkalimetry, Iodometry etc.
5. Determination of rate of reation in zero, first order reations.
6. Determination of physical constants used as criteria of purity like melting point,
boiling point, weight per ml, refractive index and viscosity.
7. Determination of pH, potentiometric and dead stop endpoint technique.
8. Preparation of buffers, sensitivity, specificity, precision and accuracy.
9. Tests for Purity for official compounds mentioned in IP/BP/USP.
10. Limit test for marketed formulations.
11. Functional group analysis
12. Molecular weight calculations
TOTAL: 45 PERIODS
PY3205 PHARMACEUTICAL ORGANIC CHEMISTRY LABORATORY
1. Determination of Impurities
2. Synthesis of some organic compounds involving single step reactions like
nitration, halogenation, acetylation and hydrolysis.
3. Synthesis of organic compounds involving Two steps
4. Assay of organic compounds involving acidimetry, alkalimetry, Iodometry etc.
5. Determination of rate of reation in zero, first order reations.
6. Determination of physical constants used as criteria of purity like melting point,
boiling point, weight per ml, refractive index and viscosity.
7. Determination of pH, potentiometric and dead stop endpoint technique.
8. Preparation of buffers, sensitivity, specificity, precision and accuracy.
9. Tests for Purity for official compounds mentioned in IP/BP/USP.
10. Limit test for marketed formulations.
11. Functional group analysis
12. Molecular weight calculations
TOTAL: 45 PERIODS
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