Remdesivir GS-5734 CAS 1809249-37-3 COVID-19 API High Quality
Manufacturer Commercial Supply Remdesivir and Related Intermediates with High Quality
Remdesivir CAS 1809249-37-3
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Chemical Name | Remdesivir |
Synonyms | GS-5734; 2-ethylbutyl ((S)-(((2R,3S,4R,5R)-5-(4-aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)-5-cyano-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)(phenoxy)phosphoryl)-L-alaninate |
CAS Number | 1809249-37-3 |
CAT Number | RF-API96 |
Stock Status | In Stock, Production Scale Up to Hundreds of Kilograms |
Molecular Formula | C27H35N6O8P |
Molecular Weight | 602.58 |
Density | 1.47±0.1 g/cm3 |
Brand | Ruifu Chemical |
Item | Specifications |
Appearance | White to Off-White Solid Powder |
Identification A | IR: The infrared absorption spectrum of the product should be consistent with that of the reference substance |
Identification B | HPLC Retention time similar to reference substance |
Specific Rotation | -19.0° ~ -22.0° |
Solubility | Solunle in Methanol, Sparingly Soluble in Ethanol, Slightly Soluble in Acetonitrile, Practically Insoluble in Water |
Related Substances | |
Any Individual Impurity | ≤0.10% |
Total Impurities | ≤1.0% |
RD-3.1 | ≤0.10% |
RD-C | ≤0.10% |
RD-D | ≤0.10% |
RD-E | ≤0.10% |
RP-Isomer | ≤0.10% |
Nitrophenol | ≤0.10% |
Residual Solvents | |
Methanol Dichloride | ≤6000ppm |
Acetone | ≤5000ppm |
Isopropyl Alcohol | ≤5000ppm |
Acetonitrile | ≤410ppm |
Dichloromethane | ≤600ppm |
Methyl tert Butyl Ether | ≤5000ppm |
Ethyl Acetate | ≤5000ppm |
Tetrahydrofuran | ≤720ppm |
n-Heptane | ≤5000ppm |
Assay | 98.0%~102.0% (Calculated on the dried basis) |
Total Aerobic Counts | |
Aerobic Bacteria | ≤100cfu/g |
Yeast and Mould | ≤10cfu/g |
E. Coil | Negative |
Bacterial Endotoxin | ≤1.0EU |
Heavy Metals | ≤20ppm |
Test Standard | Enterprise Standard |
Usage | API, COVID-19 |
Package: Bottle, Aluminum foil bag, Cardboard drum, 25kg/Drum, or according to customer's requirement.
Storage Condition: Store in sealed containers at cool and dry place; Protect from light, moisture and pest infestation.
Remdesivir (CAS 1809249-37-3), sold under the brand name Veklury, is a broad-spectrum antiviral medication developed by the biopharmaceutical company Gilead Sciences. It is administered via injection into a vein. During the COVID-19 pandemic, remdesivir was approved or authorized for emergency use to treat COVID-19 in around 50 countries. Updated guidelines from the World Health Organization in November 2020 include a conditional recommendation against the use of Remdesivir for the treatment of COVID-19. Remdesivir was originally developed to treat hepatitis C, and was subsequently investigated for Ebola virus disease and Marburg virus infections before being studied as a post-infection treatment for COVID-19. The most common side effect in healthy volunteers is raised blood levels of liver enzymes (a sign of liver problems). The most common side effect in people with COVID-19 is nausea. Side effects may include liver inflammation and an infusion-related reaction with nausea, low blood pressure, and sweating. Remdesivir is a prodrug that is intended to allow intracellular delivery of GS-441524 monophosphate and subsequent biotransformation into GS-441524 triphosphate, a ribonucleotide analogue inhibitor of viral RNA polymerase.