Sitagliptin Phosphate Monohydrate Intermediate CAS 486460-21-3 Purity >99.0% (HPLC) Factory High Quality

Short Description:

Chemical Name: 3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine Hydrochloride 

CAS: 486460-21-3

Purity: >99.0% (HPLC)

Appearance: White to Light Yellow Powder

Intermediate of Sitagliptin Phosphate Monohydrate (CAS: 654671-77-9) for the treatment of type II diabetes mellitus

E-Mail: alvin@ruifuchem.com


Product Detail

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Description:

Chemical Properties:

Chemical Name 3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine Hydrochloride
Synonyms Sitagliptin Phosphate Monohydrate Intermediate
CAS Number 486460-21-3
CAT Number RF-PI1194
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C6H7F3N4
Molecular Weight 192.14
Boiling Point 266℃
Brand Ruifu Chemical

Specifications:

Item Specifications
Appearance White to Light Yellow Powder
Identification The UV absorption spectrum of the standard sample exhibits maximum&minimum at same wavelengths
Identification HPLC: Retention time Similar
Loss on Drying <2.00%
Ordinary Impurities <1.00%
Purity / Analysis Method >99.0% (HPLC) 
Test Standard Enterprise Standard
Usage Intermediate of Sitagliptin Phosphate Monohydrate (CAS: 654671-77-9)

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:

3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine Hydrochloride (CAS: 486460-21-3) is an intermediate of Sitagliptin Phosphate Monohydrate (CAS: 654671-77-9) for the treatment of type II diabetes mellitus. Sitagliptin is approved by the FDA as an adjunct to diet and exercise to improve glycaemic control in patients with T2DM, either as a monotherapy, or in combination with Metformin or a peroxisome proliferatoractivated receptor-γ agonist (for example, thiazolidinediones) when the single agent does not provide adequate glycaemic control.

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