Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C22H24N2O9.ClH |
Molecular Weight | 496.895 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 6 / 6 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.[H][C@@]12[C@@H](O)[C@@]3([H])C(C(=O)C4=C(O)C=CC=C4[C@@]3(C)O)=C(O)[C@]1(O)C(=O)C(C(N)=O)=C(O)[C@H]2N(C)C
InChI
InChIKey=UBDNTYUBJLXUNN-IFLJXUKPSA-N
InChI=1S/C22H24N2O9.ClH/c1-21(32)7-5-4-6-8(25)9(7)15(26)10-12(21)17(28)13-14(24(2)3)16(27)11(20(23)31)19(30)22(13,33)18(10)29;/h4-6,12-14,17,25,27-29,32-33H,1-3H3,(H2,23,31);1H/t12-,13-,14+,17+,21-,22+;/m1./s1
Molecular Formula | C22H24N2O9 |
Molecular Weight | 460.434 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 5 / 6 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Molecular Formula | ClH |
Molecular Weight | 36.461 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:00:38 UTC 2023
by
admin
on
Fri Dec 15 15:00:38 UTC 2023
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Record UNII |
4U7K4N52ZM
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Record Status |
Validated (UNII)
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Record Version |
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-
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Classification Tree | Code System | Code | ||
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CFR |
21 CFR 520.1660B
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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CFR |
21 CFR 520.1660C
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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CFR |
21 CFR 333.120
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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CFR |
21 CFR 522.1662
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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EPA PESTICIDE CODE |
6308
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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CFR |
21 CFR 522.1662A
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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NCI_THESAURUS |
C1595
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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CFR |
21 CFR 522.1662B
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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Code System | Code | Type | Description | ||
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DTXSID5021097
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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PRIMARY | |||
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oxytetracycline hydrochloride
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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PRIMARY | |||
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100000092050
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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PRIMARY | |||
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4U7K4N52ZM
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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PRIMARY | |||
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C47649
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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PRIMARY | |||
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OXYTETRACYCLINE HYDROCHLORIDE
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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PRIMARY | Description: A yellow, crystalline powder; odourless. Solubility: Soluble in 2 parts of water and in 45 parts of ethanol (~750 g/l) TS; practically insoluble in ether R. Category: Antibacterial drug. Storage: Oxytetracycline hydrochloride should be kept in a tightly closed container, protected from light. Labelling: The designation sterile Oxytetracycline hydrochloride indicates that the substance complies with the additionalrequirements for sterile Oxytetracycline hydrochloride and may be used for parenteral administration or for other sterile applications. Additional information: Oxytetracycline hydrochloride is hygroscopic. Even in the absence of light, it is gradually degraded onexposure to a humid atmosphere, the decomposition being faster at higher temperatures. Dissolved in water it becomes turbid onstanding owing to the separation of the base caused through partial hydrolysis of the hydrochloride. It deteriorates in solutions ofpH below 2, and is rapidly destroyed by alkali hydroxide solutions. Definition: Oxytetracycline hydrochloride contains not less than 870 International Units of Oxytetracycline per mg, calculated withreference to the anhydrous substance. | ||
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1491015
Created by
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4U7K4N52ZM
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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PRIMARY | |||
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218-161-2
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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m8345
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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PRIMARY | Merck Index | ||
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CHEMBL1517
Created by
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SUB14740MIG
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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PRIMARY | |||
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15000-39-2
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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NON-SPECIFIC STOICHIOMETRY | |||
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2058-46-0
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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PRIMARY | |||
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DBSALT000645
Created by
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PRIMARY | |||
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4780
Created by
admin on Fri Dec 15 15:00:38 UTC 2023 , Edited by admin on Fri Dec 15 15:00:38 UTC 2023
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PRIMARY | RxNorm |
Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE | |||
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BASIS OF STRENGTH->SUBSTANCE |
ASSAY (HPLC)
USP
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BASIS OF STRENGTH->SUBSTANCE |
ASSAY (HPLC)
EP
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Related Record | Type | Details | ||
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
total of impurities D, E and F (eluting between the latter two): not more than the area of the peak due to impurity E in the chromatogram obtained with reference solution (g) (2.0 per cent)
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
total of impurities D, E and F (eluting between the latter two): not more than the area of the peak due to impurity E in the chromatogram obtained with reference solution (g) (2.0 per cent)
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
total of impurities D, E and F (eluting between the latter two): not more than the area of the peak due to impurity E in the chromatogram obtained with reference solution (g) (2.0 per cent)
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
not more than 4 times the area of the peak due to impurity A in the chromatogram obtained with reference solution
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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Related Record | Type | Details | ||
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ACTIVE MOIETY |