CAS 5391-39-9 C5H8N2O2 1-Acetyl-2-imidazolidinone 99%

Product Details
Customization: Available
CAS No.: 5391-39-9
Formula: C5H8N2O2
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Management System Certification
ISO 9001, ISO 20000
  • CAS 5391-39-9 C5H8N2O2 1-Acetyl-2-imidazolidinone 99%
  • CAS 5391-39-9 C5H8N2O2 1-Acetyl-2-imidazolidinone 99%
  • CAS 5391-39-9 C5H8N2O2 1-Acetyl-2-imidazolidinone 99%
  • CAS 5391-39-9 C5H8N2O2 1-Acetyl-2-imidazolidinone 99%
  • CAS 5391-39-9 C5H8N2O2 1-Acetyl-2-imidazolidinone 99%
  • CAS 5391-39-9 C5H8N2O2 1-Acetyl-2-imidazolidinone 99%
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Basic Info.

Model NO.
1-Acetyl-2-imidazolidinone
EINECS
226-388-3
Type
Pharmaceutical Intermediates
Appearance
Powder
Quality
Refined
Colour
White
Transport Package
25kg Cartons or Kraft Paper Sacks
Specification
25kg
Trademark
Good-brand
Origin
China
HS Code
2933990090

Product Description

China 1-Acetyl-2-imidazolidinone High-quality supplier
CAS 5391-39-9 C5H8N2O2 1-Acetyl-2-imidazolidinone 99%
 
Product name  1-Acetyl-2-imidazolidinone
CAS Number
5391-39-9
Synonyms  1-ethanoylimidazolidin-2-one;N-acetyl-2-iMidazolidazolidinone;Clonidine IMpurity-A(BP);Clonidine Impurity A;2-Imidazolidinone,1-acetyl-;n-acetyl-2-imidazolidinone;RARECHEM AQ NN 0041;ACETYL IMIDAZO-2-ONE
Molecular formula C5H8N2O2
Molecular weight 128.13
Purity  99%
Appearance  White powder
EINECS number  226-388-3

product usage

N-Acetyl-2-imidazolidinone (colistin EP impurity A) is a synthetic reagent used to prepare tris[14C]-labeled moxonidine, which is an anti-hypertensive compound. 
 

Pharmaceutical intermediates, mainly used in the synthesis of new penicillin.

 


CAS 5391-39-9 C5H8N2O2 1-Acetyl-2-imidazolidinone 99%
CAS 5391-39-9 C5H8N2O2 1-Acetyl-2-imidazolidinone 99%
 
CAS 5391-39-9 C5H8N2O2 1-Acetyl-2-imidazolidinone 99%
CAS 5391-39-9 C5H8N2O2 1-Acetyl-2-imidazolidinone 99%

Quality Control
        Quality Management Department consists of Quality Assurance (QA) and Quality Control (QC), which is independent from production and manages all activities related to quality. The quality management department is leaded directly by General Manager.
       All the products must be examined and confirmed whether released or rejected by quality management department.
       All the inspection record and product record must be collected in the technology archives room.
      The company implements the stringent QA/QC system that covers the whole line from supplier audit, procurement, and production, to shipment and distribution.
       Its operation complies with China's GMP, even beyond it. It has passed 8 GMP inspections by Chinese regulatory bodies, as well as GMP certifications of Brazil, Egypt, Indonesia, and Pakistan.

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