Talk:Quantitative NMR
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Contents
1
Regulations
1.1
EU
1.2
US
1.3
Japan
2
Theoretical Basics of qNMR Analysis
2.1
Metrology
2.2
High Precision Measurements
2.3
Reference Standards
2.4
Parameter and Risk Assessment
2.5
Traceability
3
Practical Basics of qNMR Analysis
3.1
Sample Preparation
3.1.1
Sample Weight
3.1.2
Solvents
3.2
qNMR Analysis
3.3
Spectrum Evaluation
3.3.1
Phase Correction
3.3.2
Baseline Correction
3.3.3
Integration
3.4
Quantification Techniques
3.4.1
Internal Standard
3.4.2
External Standard
3.4.3
Standard Addition
3.4.4
PULCON
3.4.5
ERETIC
3.4.6
Tube in Tube
3.5
Validation
3.5.1
Nomenclature
3.5.2
Validation Process
3.5.3
GLP, GMP
3.5.4
System Suitability Test
3.6
Proficiency Tests
3.7
Quantitative Heteronuclear Analysis
3.7.1
15
N qNMR
3.7.2
19
F qNMR
3.7.3
31
P qNMR
3.8
Education and Training
3.9
Applications
3.9.1
Food Screener
3.9.2
Lipid Analysis
3.9.3
Pharmaceuticals
3.9.4
Natural Materials
3.9.5
Polymer in Solutions
Regulations
EU
European Pharmacopeia
Arzneimittelbuch
US
US Pharmacopoeia
Japan
Japanese Pharmacopoeia
Theoretical Basics of qNMR Analysis
Metrology
High Precision Measurements
Reference Standards
Parameter and Risk Assessment
Traceability
Practical Basics of qNMR Analysis
Sample Preparation
Sample Weight
Solvents
qNMR Analysis
Spectrum Evaluation
Phase Correction
Baseline Correction
Integration
Quantification Techniques
Internal Standard
External Standard
Standard Addition
PULCON
ERETIC
Tube in Tube
Validation
Nomenclature
Validation Process
GLP, GMP
System Suitability Test
Proficiency Tests
Quantitative Heteronuclear Analysis
15
N qNMR
19
F qNMR
31
P qNMR
Education and Training
Applications
Food Screener
Lipid Analysis
Pharmaceuticals
Natural Materials
Polymer in Solutions
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