Dexamethasone 21-phosphate disodium salt

$ 600.00 /1Kg/Bag

Min. Order1Kg/Bag
Purity99%
Cas No2392-39-4
Supply Ability20 Tons
Update time2020-11-16

Longyan Tianhua Biological Technology Co., Ltd

5YR

China

Chemical Properties

Product Name	Dexamethasone 21-phosphate disodium salt
CAS No	2392-39-4
EC-No	219-243-0
Min. Order	1Kg/Bag
Purity	99%
Supply Ability	20 Tons
Release date	2020/11/16

Dexamethasone 21-phosphate disodium salt Basic information

Summary Anti-inflammatory drugs Characteristic Pharmacology effect Pharmacokinetics Adverse Reaction Medicine interactions Precautions Special people medication Medication contraindication Dosage Storage Usage References

Product Name:	Dexamethasone 21-phosphate disodium salt
Synonyms:	decadronphosphate;dexadreson;dexagro;dexamethasonedisodiumphosphate;disodiumdexamethasonephosphate;disodiumsalt,(11beta,16alpha)-y);megacort;pregna-1,4-diene-3,20-dione,9-fluoro-11,17-dihydroxy-16-methyl-21-(phosphonoox
CAS:	2392-39-4
MF:	C22H28FNa2O8P
MW:	516.4
EINECS:	219-243-0
Product Categories:	Immunomodulators and AntibioticsLipids;Steroids (C21) and Derivatives;Immune Cell Signaling and Blood;Immune System Regulation;Sterols;Pharmaceutical intermediate;API;HEXADROL;Hormone Drugs
Mol File:	2392-39-4.mol

Dexamethasone 21-phosphate disodium salt Chemical Properties

Melting point	233-235 °C
alpha	D +57° (water); D25 +74 ±4° (calcd on water-free and alcohol-free basis, concn of 10 mg/ml): USP XIX, p 124
storage temp.	2-8°C
solubility	H₂O: 50 mg/mL, clear, faintly yellow
form	White Powder
color	white to off-white
Water Solubility	Soluble in water. Slightly soluble in ethanol. Insoluble in dichloromethane.
Merck	13,2960
InChIKey	PLCQGRYPOISRTQ-FCJDYXGNSA-L
CAS DataBase Reference	2392-39-4(CAS DataBase Reference)
EPA Substance Registry System	Pregna-1,4-diene- 3,20-dione, 9-fluoro-11,17-dihydroxy-16- methyl-21-(phosphonooxy)-, disodium salt, (11.beta.,16.alpha.)-(2392-39-4)

Safety Information

Hazard Codes	Xn
Risk Statements	22-40-63
Safety Statements	36/37/39
WGK Germany	3
RTECS	TU4056000
F	3-10
TSCA	Yes

Dexamethasone 21-phosphate disodium salt Usage And Synthesis

Summary	Dexamethasone 21-phosphate disodium salt is a system glucocorticoid with anti-inflammatory properties, is the pro-drug which is converted to dexamethasone in vivo. It stimulates uptake of glutamine in the cerebral cortex and induces apoptosis. In addition to binding to specific nuclear steroid receptors, dexamethasone also interferes with NF-kB activation and apoptotic pathways. It is freely soluble in water, slightly soluble in ethanol, and insoluble in chloroform and in ether. It is an inhibitor of the sodium phosphate symporter and GR activator. Additionally, it serves as an activator of food, medicine, glucocorticoid and anti inflammatory.
Anti-inflammatory drugs	Dexamethasone sodium phosphate (DSP), chemical name 16a-methyl-11β,17a,21-trihydroxy-9a-fluoropregna-1,4-diene-3,20-dione-21-Phosphate disodium salt, belongs to the adrenal cortex hormones. It has the effect of antiphlogosis by stabilizing the lysosomal membrane, reducing the release of lysosomal hydrolase; inhibiting the formation of inflammation-induced material bradykinin, serotonin and prostaglandin, increasing the stability of mast cells particles, reducing the release of histamine, concentrate blood vessels, stop white blood cells and macrophages from migrating outside of the blood vessels, etc. It can inhibit macrophage function to play immunization function and inhibit the formation of fibroblasts which is conducive to prevent corneal scar. When used for trauma, it can stop scar from forming and protect eyesight. It can inhibit or reduce the formation of new vessel in the cornea and conjunctiva disease and alleviate rejection reaction and scar formation in local use. In clinical treatment it can be used for autoimmune diseases, allergies, inflammation, rheumatism, asthma, ophthalmology and dermatology and other diseases.
Characteristic	This product is white or off-white powder; odorless with slightly bitter taste and hygroscopicity. It can dissolve in water or methanol but is almost insoluble in acetone or ether. Melting point 233-235 ℃.
Pharmacology effect	Antiinflammatory effect This product can relieve and prevent the reaction of organization to inflammation. In the early stage of acute inflammation, it can reduce the exudation of local edema by inhibiting capillary permeability, leukocyte infiltration and phagocytosis and reducing the release of various inflammatory mediators In the late inflammatory phase, it can inhibit capillary and fibroblast proliferation and collagen protein synthesis to prevent adhesion and scar formation. Immunity inhibition and anti-allergic effects This product can prevent or inhibit cell-mediated immune response, delayed allergic reactions,reduce the number of T lymphocytes, monocytes and brucella cells, reduce the integration ability between immunoglobulin and cell surface receptors and inhibit interleukin synthesis and release, thus inhibting the transformation of T lymphocytes to lymphocyte and pathological changes caused by allergic reactions such as allergic congestion, edema, exudation, rash, smooth muscle spasm, cell damage. and so on. This product also prevents the immune replenishment from getting through the basement membrane and can reduce the complement component and immunoglobulin concentration. In addition it can inhibit the transplant rejection reaction of tissue and organ and has certain short-term effect on autoimmune diseases. The treatment effect on ophthalmic diseases Inhibition of corneal epithelial regeneration, in the cornea, conjunctival disease can inhibit or reduce the formation of new blood vessels.
Pharmacokinetics	This product is adrenal corticosteroid drugs. Its effect is similar to hydrocortisone but stronger with anti-inflammatory effect 40-50 times that of hydrocortisone and more notable effect of anti-inflammatory, anti-allergy, anti-shock than prednisone. It has quick efficacy and less side effects improving the body function in short time especially for the forst aid in critical illnesses. This product affects sugar metabolism and has strong function of anti-inflammatory, anti-inflammatory, anti-inflammatory and anti-allergy It affects water and sodium retention slightly and has strong inhibitory effect on pituitary-adrenal so it just causes slight side effects such as edema, hypertension,muscle weakness and so on. This product transpires through kidneys in urine after metabolic transformation in liver so the drug's plasma half-life can extend for people with liver and renal dysfunction. The concentration reaches plasma peak one hour after intramuscular and plasma protein binding rate is lower than other corticosteroids drug.
Adverse Reaction	The main adverse reactions of this product is concurrent infection, including fungi, tuberculosis, staphylococcus, proteus, pseudomonas aeruginosa and a variety of herpes virus Long-term use can cause iatrogenic Cushing's syndrome. For patients suffering from chronic wasting disease or mental disorders before, such mental symptoms may occur:euphoria, excitement, delirium, anxiety, orientation disorder or inhibition. Some patients with long-term local drug use may suffer hormone glaucoma and hormone cataracts. Glucocorticoid withdrawal syndrome. Sometimes the patient stop taking medicine may suffer dizziness, fainting tendencies, abdominal pain or back pain, fever, loss of appetite, nausea, vomiting, muscle or joint pain, headache, fatigue, weakness, which can be considered to be glucocorticoid-dependent syndrome adrenal insufficiency and the recurrence of original disease are excluded after careful examination.
Medicine interactions	The decomposition of this product can be speeded and metabolic promotion is weakened if taken with barbiturates, phenytoin, rifampicin and other liver enzyme inducer The toxicity increases combined with salicylic acid The product can reduce the effect of anticoagulant and oral hypoglycemic and attention should be paid adjust the dose. Incompatible with hydrochloric vancomycin
Precautions	Patients with tuberculosis, acute bacterial or viral infections must be given appropriate anti-infective treatment. For eye infections combined with effective antibiotics. Patients with corneal ulcers are not permitted. When patient’s condition turns better dose times should be gradually reduced in case of recurrence. Patients with diabetes, osteoporosis, cirrhosis, renal dysfunction, and hypothyroidism should be cautious to take. After long-term medication, dosage should be gradually reduced before stop. Athletes with caution.
Special people medication	Pregnant women and lactatinal women medication This product with teratogenic effect in animal test can increase the probability of placental insufficiency, neonatal weight loss or stillbirth. So the pregnant women should weight advantages and disadvantages before taking it. Nannie receiving high-dose administration should not breast feed, in case of drug transpiring through milk resulting in infant growth inhibition, adrenal function inefficiency and other adverse reactions Children medication Be careful in giving infant adrental cortex hormones administration because it can inhibit infant from growth and development. If long-term use is necessary, short-acting or medium-acting agents should be used instead of long-acting dexamethasone preparations and changes in intracranial pressure should be observed. Old people medication Easy to suffer high blood pressure and diabetes. For old patients especially after-menopaue women the osteoporosis.tends to be severer.
Medication contraindication	Patients with allergic history to this product and adrenal corticosteroids should not be permitted and in special case pros and cons should be weighed before use .Pay attention to the deterioration of the disease: It is not suitable for patients with hypertension, thrombosis, stomach and duodenal ulcer, psychosis, electrolyte metabolism, myocardial infarction , visceral surgery, glaucoma and so on.

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Dexamethasone 21-phosphate disodium salt

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