2-Amino-1-Pyrroline Hydrochloride CAS 7544-75-4 Purity >99.5% (HPLC) Tipiracil Hydrochloride Intermediate Factory

Chemical Name: 2-Amino-1-Pyrroline Hydrochloride CAS: 7544-75-4 Purity: >99.5% (HPLC)   Appearance: White Powder  Intermediate of Tipiracil Hydrochloride (CAS: 183204-72-0) in the treatment of Rectal Cancer Mobile/Wechat/WhatsApp: +86-15026746401 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 moistureManufacturer Supply, High Quality and Competitive Price Tipiracil Hydrochloride (CAS: 183204-72-0) Related Intermediates 6-(Chloromethyl)uracil CAS: 18592-13-7 6-(Hydroxymethyl)uracil CAS: 22126-44-9  2-Amino-1-Pyrroline Hydrochloride CAS 7544-75-4

Item

Specifications

Results

 Appearance

 White Powder

White Powder

Purity / Analysis Method

>99.5% (HPLC)

99.8%

Largest Single Impurity

<0.50%

0.09%

 Water Content (K.F)

<0.50%

0.45%

Proton NMR Spectrum

Conforms to Structure

Conforms

Test Standard

Enterprise Standard

Usage

Intermediate of Tipiracil Hydrochloride (CAS: 183204-72-0)

Description:

Specifications:

Package & Storage:

Chemical Name 2-Amino-1-Pyrroline Hydrochloride
Synonyms 3,4-Dihydro-2H-Pyrrol-5-Amine Hydrochloride; 2-Aminopyrrolidine HCl
CAS Number 7544-75-4
CAT Number RF-PI1838
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C4H8N2·HCl
Molecular Weight 120.58
Melting Point 171.0 to 175.0℃
Sensitive Hygroscopic
Brand Ruifu Chemical

Advantages:

FAQ:

Application:

2-Amino-1-Pyrroline Hydrochloride (CAS: 7544-75-4) is a heterocyclic organic compound, which can be used as a pharmaceutical intermediate. 2-Amino-1-Pyrroline Hydrochloride is an intermediate of Tipiracil Hydrochloride (CAS: 183204-72-0) in the treatment of Rectal Cancer. Tipiracil Hydrochloride is a potent and competitive inhibitor of thymidine phosphorylase (TPase) with an IC50 value of 35 nM for human placental TPase. It is selective for TPase over other pyrimidine-metabolizing enzymes (IC50s = >1 mM for UPase, OPRTase, TK, and DPDase). TPI inhibits the phosphorolysis and degradation of trifluorothymidine, a cytotoxic nucleoside, in human breast and colon carcinoma tumor samples. Oral administration of TPI (12.5-50 mg/kg) enhances the anti-tumor activity of trifluorothymidine in a mouse AZ-521 stomach cancer xenograft model. Formulations containing TPI have been used for the treatment of metastatic colorectal cancer.

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