High quality USP 39/EP 9.0 /BP 2012 GMP DMF FDA Flavin adenine dinucleotide CAS:146-14-5 CAS NO.146-14-5
- Min.Order: 1 Kilogram
- Payment Terms: L/C,D/A,D/P,T/T,
- Product Details
Keywords
- FLAVIN ADENINE DINUCLEOTIDE
- 146-14-5
- 99% FLAVIN ADENINE DINUCLEOTIDE
Quick Details
- ProName: High quality USP 39/EP 9.0 /BP 2012 GM...
- CasNo: 146-14-5
- Molecular Formula: C13H18O7
- Appearance: powder
- Application: in pharma and cosmetics cas 138-52-3
- DeliveryTime: 2 days
- PackAge: bags
- Port: Guangzhou
- ProductionCapacity: 4000 Kilogram/Day
- Purity: 99%
- Storage: sealed
- Transportation: by air
- LimitNum: 1 Kilogram
- Grade: Industrial Grade,Food Grade,Pharma Gra...
- cas: 138-52-3
Superiority
Item | Standard | Test Results | |
Identification |
A.H-NMR:Comply with the structure |
Complies |
|
B.LC-MS:Comply with the structure |
Complies |
||
C.The IR spectrum of sample should be identical with that of reference standard; |
Complies |
||
D.HPLC-ESI-MS The retention time of the major peak in the chromatogram of the Assay preparation corresponds to that in the chromatogram of the Standard preparation, as obtained in the Assay. |
Complies |
||
Crystallinity |
meets the requirements. |
Complies |
|
Loss on drying |
≤2.0% |
0.19% |
|
Heavy metals |
≤10 ppm |
<10ppm |
|
Water |
≤1.0% |
0.1% |
|
Sulphated ash |
≤0.5%, determined on 1.0 g. |
0.009% |
|
Related substances |
Unspecified impurities: for each impurity |
≤0.10% |
<0.10% |
Total Impurity |
≤0.5% |
0.18% |
|
Purity |
≥99.0% |
99.7% |
|
Assay |
99.0%~101.0% (anhydrous substance). |
99.8% |
|
Microbiological Analysis |
|||
Total plate count |
≤1000cfu/g |
Complies |
|
Yeast and Moulds |
≤100cfu/g |
Complies |
|
E. Coli. |
Absent |
Negative |
|
Salmonella |
Absent |
Negative |
|
S.aureus |
Absent |
Negative |
|
Storage |
Preserve in well-closed, light-resistant and airtight containers. |
Complies |
Details
Item | Standard | Test Results | |
Identification |
A.H-NMR:Comply with the structure |
Complies |
|
B.LC-MS:Comply with the structure |
Complies |
||
C.The IR spectrum of sample should be identical with that of reference standard; |
Complies |
||
D.HPLC-ESI-MS The retention time of the major peak in the chromatogram of the Assay preparation corresponds to that in the chromatogram of the Standard preparation, as obtained in the Assay. |
Complies |
||
Crystallinity |
meets the requirements. |
Complies |
|
Loss on drying |
≤2.0% |
0.19% |
|
Heavy metals |
≤10 ppm |
<10ppm |
|
Water |
≤1.0% |
0.1% |
|
Sulphated ash |
≤0.5%, determined on 1.0 g. |
0.009% |
|
Related substances |
Unspecified impurities: for each impurity |
≤0.10% |
<0.10% |
Total Impurity |
≤0.5% |
0.18% |
|
Purity |
≥99.0% |
99.7% |
|
Assay |
99.0%~101.0% (anhydrous substance). |
99.8% |
|
Microbiological Analysis |
|||
Total plate count |
≤1000cfu/g |
Complies |
|
Yeast and Moulds |
≤100cfu/g |
Complies |
|
E. Coli. |
Absent |
Negative |
|
Salmonella |
Absent |
Negative |
|
S.aureus |
Absent |
Negative |
|
Storage |
Preserve in well-closed, light-resistant and airtight containers. |
Complies |