Properties: Crystals from ether, mp 262-264°; mp 268-271° (Arth, 1961). [a]D25 +77.5° (dioxane). Soly in water (25°): 10 mg/100 ml. Sol in acetone, ethanol, chloroform.
Melting point: mp 262-264°; mp 268-271° (Arth, 1961)
Optical Rotation: [a]D25 +77.5° (dioxane)
Derivative Type: 21-Acetate
CAS Registry Number: 1177-87-3
Trademarks: Decadronal (Merck Co.); Decadron-LA (Merck Co.); Dectancyl (Sanofi-Aventis)
Percent Composition: C 66.34%, H 7.19%, F 4.37%, O 22.09%
Properties: Crystals, mp 215-221° (Arth, 1958); mp 229-231° (Oliveto); mp 238-240° (Arth, 1961). [a]D25 +73° (chloroform) (Arth, 1958); [a]D +77.6° (Oliveto). uv max: 239 nm (e 14900).
Melting point: mp 215-221° (Arth, 1958); mp 229-231° (Oliveto); mp 238-240° (Arth, 1961)
Optical Rotation: [a]D25 +73° (chloroform) (Arth, 1958); [a]D +77.6° (Oliveto)
Absorption maximum: uv max: 239 nm (e 14900)
Derivative Type: 21-Phosphate disodium salt
CAS Registry Number: 2392-39-4
Additional Names: Dexamethasone 21-(dihydrogen phosphate) disodium salt; dexamethasone sodium phosphate
Trademarks: Ak-Dex (Akorn); Dalalone (Forest); Desocort (Bausch Lomb); Dexabene (Merckle); Hexadrol (Organon); Oradexon (Organon); Orgadrone (Han Wha); SoluDecadron (Merck Co.); Soldesam (Farmacologico); Solupen N (Winzer); Totocortin (Winzer)
Percent Composition: C 51.17%, H 5.47%, F 3.68%, Na 8.90%, O 24.79%, P 6.00%
Literature References: Used as an injectable form of dexamethasone. Prepn: Chemerda et al.,
US
2939873 (1960 to Merck Co.); Irmscher, Chem. Ind. (London)
1961, 1035.
Properties: Crystals, mp 233-235°. [a]D +57° (water). Also reported as [a]D25 +74 ±4° (calcd on water-free and alcohol-free basis, concn of 10 mg/ml): USP
XIX, p 124. uv max (ethanol): 238-239 nm (e 14000). Sol in water.
Melting point: mp 233-235°
Optical Rotation: [a]D +57° (water); [a]D25 +74 ±4° (calcd on water-free and alcohol-free basis, concn of 10 mg/ml): USP
XIX, p 124
Absorption maximum: uv max (ethanol): 238-239 nm (e 14000)
Derivative Type: 21-Isonicotinate
Additional Names: Dexamethasone 21-(4-pyridinecarboxylate)
Trademarks: Auxisone (Boehringer, Ing.)
Percent Composition: C 67.59%, H 6.48%, F 3.82%, N 2.82%, O 19.29%
Properties: Crystals, mp 250-252°. [a]D27 +183.5° (dioxane).
Melting point: mp 250-252°
Optical Rotation: [a]D27 +183.5° (dioxane)
Derivative Type: 17,21-Dipropionate Trademarks: Methaderm (Taiho)
Percent Composition: C 66.65%, H 7.39%, F 3.77%, O 22.20%
Therap-Cat: Glucocorticoid; anti-inflammatory. Diagnostic aid (Cushing's syndrome, depression).
Therap-Cat-Vet: Glucocorticoid; anti-inflammatory.
Keywords: Antiallergic (Steroidal, Nasal); Antiasthmatic (Steroidal, Inhalant); Diagnostic Aid; Glucocorticoid.
产品链接: 50-02-2››