Detail of > 24390-14-5
- MSDS Download

- CAS Number:
- 24390-14-5
- Name:
Doxycycline hyclate
- Formula:
- C22H24N2O8.HCl
- Molecular Structure:

- Synonyms:
- Vibramycin (TN);Doxycycline hyclate (USP);(2Z,4S,4aR,5S,5aR,6R,12aS)-2-(amino-hydroxy-methylidene)-4-dimethylamino-5,10,11,12a-tetrahydroxy-6-methyl-4a,5,5a,6-tetrahydro-4H-tetracene-1,3,12-trione; ethanol; hydrate; dihydrochloride;Doxycycline hydrochloride hemiethanolate hemihydrate;DOXY;Doryx (TN);Doryx;Doxycycline Hcl;Dipivefrin HCl;
- Molecular Weight:
- 480.90
- Boiling Point:
- 685.2 °C at 760 mmHg
- Flash Point:
- 368.2 °C
- Hazard Symbols:
Xn- Risk Codes:
- 22-36/37/38
- Safety:
- 26Details
- Deleted CAS:
- 62149-53-5
Related products
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Reference
- Antifungal activity of four tetracycline analogs against Candida albicans in vitro: potentiation by amphotericin B
- Antifungal activity of four tetracycline analogs against Candida albicans in vitro: potentiation by amphotericin B. Lew, Michael A.; Beckett, Kevin M.; Levin, Myron J. (Div. Clin. Microbiol., Sidney Farber Cancer Inst., Boston, Mass., USA). J. Infect. Dis., 136(2), 263-70 (English) 1977. CODEN: JIDIAQ. DOCUMENT TYPE: Journal CA Section: 3 (Biochemical Interactions) The antifungal activities of 4 tetracyclines in combination with amphotericin B (I) [1397-89-3] were detd. against 20 strains of C. albicans. When a microtiter checkerboard technique was used, minocycline [10118-90-8] (.ltoreq.10 .mu.g/mL) acted synergistically with I against all strains, whereas doxycycline hyclate [24390-14-5] had a reduced effect, and demeclocycline [127-33-3] and tetracycline [60-54-8] had no potentiating effect at this concn. Killing-curve expts. with 2 strains of C. albicans demonstrated that the combination of minocycline and I produced a decrease in no. of colony-forming units of >2 logs in 4 h and a 4-log decrease in 24 h at concns. (minocycline, 0.64 .mu.g/mL; I, 0.1 .mu.g/mL) that were subinhibitory when each agent was used alone. The killing-curve technique indicated that doxycycline had an intermediate degree of synergistic activity, whereas tetracycline had no synergistic activity at clin. relevant concns.
- Doxycycline capsules
- Doxycycline capsules. Struengmann, A. (Distributa S. A., Luxembourg). Belg. BE 897510 A2 1 Dec 1983, 9 pp. (Dutch). (Belgium). CODEN: BEXXAL. ICI: A61; A61. APPLICATION: BE 21-335 10 Aug 1983. PRIORITY: LU 82-84526 10 Dec 1982. DOCUMENT TYPE: Patent CA Section: 63 (Pharmaceuticals) Sucrose [57-50-1]-corn starch [9005-25-8] pellets are sprayed with a mixt. of doxycycline-HCl.0.5 EtOH.H2O (I) [24390-14-5] and PVP [9003-39-8] until the ratio of doxycycline [564-25-0] to pellets is about 0.7:1, coated with Eudragit E [24938-16-7] dried, and used for filling capsules. For example, a soln. of sucrose 50.0 and corn starch 25.0 in water 10 kg was sprayed onto 25.0 kg cryst. sucrose at 80° and the resulting pellets, after drying, were sieved to sep. the 0.5-0.65 mm fraction. The homogeneous mixt. of 115.4 kg I, PVP, and acetone was sprayed to 37.7 kg pellets, and the pellets were then coated with a 12.There are some commonly used reagents with their cas registry numbers 564-25-0 and 57-50-1 in this article.5% suspension of talc in Eudragit E-100, dried, and dispensed into hard gelatin capsules. The capsule content consisted of I 230.80, sucrose 62.25, corn starch 20.75, talc 5.20, Eudragit E-100 6.40, and PVP 4.60 mg. .
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