2-Amino-6-Chloropurine CAS 10310-21-1 Purity ≥99.0% (HPLC) Famciclovir Intermediate

Short Description:

Chemical Name: 2-Amino-6-Chloropurine 

CAS: 10310-21-1

Purity: ≥99.0% (HPLC)

Light Yellow to Off-White Crystalline Powder

High Quality, Commercial Production 

Intermediate for Famciclovir (CAS: 104227-87-4)

E-Mail: alvin@ruifuchem.com


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Description:

Manufacturer Supply, High Purity, Commercial Production 
Chemical Name: 2-Amino-6-Chloropurine 
CAS: 10310-21-1

Chemical Properties:

Chemical Name 2-Amino-6-Chloropurine
Synonyms 6-Chloroguanine; Famciclovir USP Related Compound F
CAS Number 10310-21-1
CAT Number RF-PI489 
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C5H4ClN5
Molecular Weight 169.57
Melting Point  >300℃ (lit.)
Solubility Solubility in 1mol/L NaOH; Very Faint Turbidity
Brand Ruifu Chemical

Specifications:

Item Specifications
Appearance Light Yellow to Off-White Crystalline Powder
Purity / Analysis Method ≥99.0% (HPLC)
Loss on Drying ≤0.50%
Sulphated Ash ≤0.20%
Guanine (RPT=0.27) ≤0.20%
Impurity (RPT=1.54) ≤0.20%
Impurity (RPT=1.75) ≤0.30%
Any Other Impurity ≤0.20%
Total Impurities ≤1.0%
Heavy Metals ≤10ppm
Test Standard Enterprise Standard
Usage Intermediate for Famciclovir (CAS: 104227-87-4)

Package & Storage:

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 moisture.

Advantages:

1

FAQ:

Application:

2-Amino-6-Chloropurine (CAS: 10310-21-1) is an intermediate of the antiviral agent Famciclovir (CAS: 104227-87-4). Famciclovir, an effective oral prodrug of the antiviral penciclovir, was launched in the UK and shortly after in the U.S.A. for the treatment of shingles (herpes zoster). Famciclovir is a synthetic purine nucleoside analogue related to guanine. As the diacetyl ester of the 6-deoxy-penciclovir, famciclovir has significantly improved oral absorption. The high selectivity of Famciclovir/Penciclovir to herpes family of viruses and their rather low toxicity may make this agent superior to other existing drugs.

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