Molnupiravir Impurity 1 CAS 3258-02-4
Product Name:N(4)-hydroxycytidine
Synonym:3,4-Dihydro-1-β-D-ribofuranosyl-4-(hydroxyimino)pyrimidin-2(1H)-one;N-Hydroxycytidine;β-D-N4-Hydroxycytidine;Beta-d-N4-hydroxycytidine;EIDD-1931;Beta-d-N4-hydroxycytidine(NHC);Molnupiravir Impurity 1
CAS NO.:3258-02-4
EINECS NO.:/
Molecular Formula:C9H13N3O6
Purity & Grade: 99%; Medicine grade
Character:White powder
Free sample:Available
Stock:In stock
Warehouse: USA/EU/AU Warehouse
MOQ & Package: 1g; Package according to demand
Shipping: Safe and fast delivery
Lead Time: 5-10 days
Store & Shelf life: Cool & dry place; 24 months
Description
Product description

Molnupiravir Impurity 1 is a structurally modified nucleoside compound and a highly valuable active nucleoside monomer for research in biochemistry and molecular biology. It is a white solid powder at room temperature, exhibits good water solubility, and is typically stored at -20°C in a sealed, light-protected environment. Its stable physicochemical properties allow for long-term preservation for various experimental studies. Structurally, N(4)-hydroxycytidine uses natural cytidine as its backbone, with the amino group at the fourth position of the cytosine base hydroxylated to form a unique hydroxyl-amino substitution structure, distinct from the molecular configuration of natural nucleosides. This special structural modification is the root of its core biological characteristics, enabling it to participate in nucleic acid synthesis and metabolism within organisms. During biological metabolism, this substance undergoes phosphorylation within cells, transforming into its activated triphosphate form, which can randomly integrate into newly formed RNA chains, disrupting the normal base pairing rules of nucleic acids. Compared to the specific pairing characteristics of natural cytidine, N(4)-hydroxycytidine can flexibly pair with guanine and adenine, thereby inducing the accumulation of base mismatches during viral nucleic acid replication, ultimately causing nucleic acid sequence mutations, genetic information disorder, and blocking the normal replication and transcription of biological genetic material.
Furthermore, related studies have found that the biological activity of N(4)-hydroxycytidine is closely related to cellular oxidative stress. It can mediate cellular oxidative damage and metabolic regulation processes by regulating intracellular reactive oxygen species levels. This characteristic makes it an important research object in the fields of cytotoxicology and oxidative biology. After years of scientific research, the molecular mechanism of action, physicochemical properties, and biological functions of this substance have been gradually verified and improved. It is now widely used in multiple research fields such as virology, molecular genetics, and biochemistry. Molnupiravir Impurity 1 is an important compound connecting basic nucleic acid theory research with applied research on antiviral mechanisms, providing a solid experimental foundation and theoretical basis for the development of novel antiviral mechanisms and the analysis of nucleic acid metabolism mechanisms.

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COA
| Test Item | Specification | Result |
| Appearance | White powder | Conforms |
| Specification | 99% | Conforms |
| Odor | Characteristic | Conforms |
| Particle size | 100% pass 80 mesh | Conforms |
| Heavy metals | ||
| Total Heavy metals | ≤10ppm | Conforms |
| Microbial | ||
| Total microbacterial count | ≤1000cfu/g | Conforms |
| Yeast &Mould | ≤100cfu/g | Conforms |
| Escherichia Coli presence | Negative | Conforms |
| Salmonella | Negative | Conforms |
| Staphylococcus | Negative | Conforms |
| Conclusion | Conform with enterprise specification | |
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Molecular Formula: C9H13N3O6
Molecular Weight: 259.21600
Exact Mass: 259.08000
PSA: 137.07000
InChIKey XCUAIINAJCDIPM-XVFCMESISA-N
SMILES O=c1nc(NO)ccn1C1OC(CO)C(O)C1O
Mechanism of action of N(4)-hydroxycytidine
Mimicking Natural Nucleosides Incorporation into Nucleic Acids
After entering the cell, they are phosphorylated to form the active triphosphate form, which is recognized by RNA polymerase and randomly incorporated into the nascent viral/host RNA chain.
Altering Base Pairing Rules
Hydroxy modification alters the base conformation, preventing specific pairing with guanine (G). It can simultaneously mispair with uracil (U) and guanine (G), causing base pairing disorder.
Inducing High-Frequency Gene Mutations
Missense mutations continuously occur throughout RNA replication and translation, resulting in a large accumulation of viral genome mutations, i.e., mutagenic effects.
Inhibiting Viral Proliferation
The continuous accumulation of mutations leads to abnormal viral protein structure and loss of function, ultimately significantly reducing viral replication capacity, achieving antiviral and viral attenuation effects.
High Concentrations Producing Cytotoxicity
Excessive incorporation into host cell RNA disrupts normal gene expression and protein synthesis, causing host cell damage.
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Transportation Time |
Shipping method |
Cargo weight requirements |
Advantage |
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3-7 days |
DHL,Germany DHL,Germany DPD, |
Suitable for under 50kg. |
We have warehouses in Germany and California, USA, and customers in Europe and America can enjoy sending goods directly from these two places. |
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7-15 days |
By Air |
Suitable for more than 50kg. |
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15-60 days |
By Sea |
Suitable for more than 500kg. |
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FAQ
01. What are the laboratory storage requirements?
Molnupiravir Impurity 1 needs to be stored at -20°C, protected from light, sealed, and frozen, avoiding repeated freeze-thaw cycles; aqueous solutions should be prepared and used immediately.
02. Is it the same substance as 5-hydroxycytidine?
No, the hydroxyl substitution positions are different: one is at position 4, and the other is at position 5, resulting in differences in structure, physicochemical properties, and biological activity.
03. Where can I buy Molnupiravir Impurity 1?
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