PriceList for 2-Bromo-4-Benzyloxy-3-nitroacetophenone - Isocytosine CAS 108-53-2 Purity ≥98.0% (HPLC) Factory High Purity – Ruifu

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PriceList for 2-Bromo-4-Benzyloxy-3-nitroacetophenone - Isocytosine CAS 108-53-2 Purity ≥98.0% (HPLC) Factory High Purity – Ruifu Detail:

Manufacturer with High Purity and Stable Quality
Chemical Name: Isocytosine
Synonyms: 2-Amino-4(1H)-pyrimidinone
CAS: 108-53-2
Appearance: White or Off-White Powder
Purity: ≥98.0% (HPLC)
Loss on Drying: ≤0.5%
Residue on Ignition: ≤0.10%

Name Isocytosine
Synonyms 2-Amino-4(1H)-pyrimidinone
CAS Number 108-53-2
CAT Number RF-PI181
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C4H5N3O
Molecular Weight 111.10
Brand Ruifu Chemical
Item Specifications
Appearance White or Off-White Powder
Purity / Analysis Method ≥98.0% (HPLC)
Melting Point 265.0 ~ 270.0℃
Loss on Drying ≤0.50%
Residue on Ignition ≤0.10%
Test Standard Enterprise Standard
Usage Pharmaceutical Intermediates; Organic Synthesis

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.

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Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of Isocytosine (CAS: 108-53-2) with high quality. It is an organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process.

Isocytosine (CAS: 108-53-2) is a useful intermediate for chemical modifications of base and sugar moieties in natural nucleosides.

Isocytosine (CAS: 108-53-2) is a pyrimidine base that is an isomer of cytosine. It is used in combination with isoguanine in studies of unnatural nucleic acid analogues of the normal base pairs in DNA.  In particular, it is used as a nucleobase of hachimoji RNA. It can be synthesized from guanidine and malic acid. Isocytosine (CAS: 108-53-2) is also used in physical chemical studies involving metal complex binding, hydrogen bonding, and tautomerism and proton transfer effects in nucleobases.


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