4,5-Dimethyl-1,3-Dioxol-2-One (DMDO) CAS 37830-90-3 Purity >99.0% (GC) Olmesartan Medoxomil Intermediate Factory

Chemical Name: 4,5-Dimethyl-1,3-Dioxol-2-One Synonyms: DMDO CAS: 37830-90-3 Purity: >99.0% (GC)   White to Light Gray to Light Yellow Powder to Crystal Intermediate of Olmesartan Medoxomil E-Mail: alvin@ruifuchem.com

Products Details

Chemical Properties:

Package: Bottle, Aluminium foil bag, 25kg/Cardboard Drum, or according to customer's requirement Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moistureRuifu Chemical Supply Olmesartan Medoxomil Intermediates With High Quality: 4,5-Dimethyl-1,3-Dioxol-2-One (DMDO) CAS 37830-90-3 4-Chloromethyl-5-Methyl-1,3-Dioxol-2-One (DMDO-Cl) CAS 80841-78-7 Ethyl 4-(1-Hydroxy-1-Methylethyl)-2-Propyl-Imidazole-5-Carboxylate CAS 144689-93-0 Diethyl 2-Propyl-1H-Imidazole-4,5-Dicarboxylate CAS 144689-94-1 Trityl Olmesartan Ethyl Ester CAS 144690-33-5 Trityl Olmesartan Acid CAS 761404-85-7 N2-Trityl Olmesartan Acid CAS 752179-89-8 Trityl Olmesartan Medoxomil CAS 144690-92-6 Olmesartan Medoxomil CAS 144689-63-4
Item Specifications
Appearance White to Light Gray to Light Yellow Powder to Crystal
Purity / Analysis Method >99.0% (GC)    
Melting Point 76.0~80.0℃
Loss on Drying <1.00%
Total Impurities <1.00%
Infrared Spectrum Conforms to Structure
Test Standard Enterprise Standard
Usage Intermediate of Olmesartan Medoxomil (CAS: 144689-63-4)

Description:

Specifications:

Package & Storage:

Chemical Name 4,5-Dimethyl-1,3-Dioxol-2-One
Synonyms DMDO
CAS Number 37830-90-3
CAT Number RF-PI1877
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C5H6O3
Molecular Weight 114.10
Brand Ruifu Chemical

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Application:

4,5-Dimethyl-1,3-Dioxol-2-One (DMDO) (CAS: 37830-90-3) is used in the preparation of Olmesartan Medoxomil (CAS: 144689-63-4). Olmesartan Medoxomil was launched in the US as Benicar@, an orally administered treatment for hypertension. Olmesartan, is a new selective and competitive nonpeptide angiotensin II type 1 receptor antagonist and potently inhibits the Ang.ll-induced pressor responses. The drug competitively inhibited binding of [125I1]-All to AT1 receptors in bovine adrenal cortical membranes, but had no effect on binding to AT2 receptors in bovine cerebellar membranes. In comparative clinical studies in patients with essential hypertension, Olmesartan reduced sitting cuff diastolic blood pressure significantly more than Losartan, Valdesartan and Ibesartan, while reductions in systolic blood pressure were similar for all treatments. Olmesartan Medoxomil was also shown to reduce blood pressure significantly more effectively than losartan and the ACE inhibitor captopril and as effectively as the pbloker atenolol.

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