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Home > Products >  High quality USP 39/EP 9.0 /BP 2012 Ceftazidime Pentahydrate CAS NO 78439-06-2

High quality USP 39/EP 9.0 /BP 2012 Ceftazidime Pentahydrate CAS NO 78439-06-2 CAS NO.78439-06-2

  • Min.Order: 100 Gram
  • Payment Terms: T/T
  • Product Details

Keywords

  • Ceftazidime Pentahydrate
  • 78439-06-2
  • CAS 78439-06-2

Quick Details

  • ProName: High quality USP 39/EP 9.0 /BP 2012 Ce...
  • CasNo: 78439-06-2
  • Molecular Formula: C22H32N6O12S2
  • Appearance: White fine powder
  • Application: Animal Pharmaceuticals
  • DeliveryTime: 3 days after the payment
  • PackAge: packing with bottle or drum
  • Port: Shanghai port
  • ProductionCapacity: 10 Metric Ton/Month
  • Purity: 99%
  • Storage: Preserve in well-closed, light-resista...
  • Transportation: 1) 25kg/drum (25kg net weight, 28kg gr...
  • LimitNum: 100 Gram

Superiority

1) Product Name: Ceftazidime pentahydrate/ceftazidime 

2) Specification: 99%

3) Testing Method: HPLC

4) Appearance:  White fine powder  

5) Introduction:  

  Ceftazidime Pentahydrate is a third generation cephalosporin antibiotic. Cephalosporins are composed of 7-aminocephalosporanic acids and are of different sizes depending on their side chain substituents. Studies show that Ceftazidime Pentahydrate has greater activity againstPseudomonas aeruginosa than it does against gram-positive cocci. 

 

Details

  Our  Referance Specification, for more details, pls contact us for COA,MSDS and certification:

  

Item Standard Test Results

Identification

A.H-NMR:Comply with the structure

Complies

B.LC-MS:Comply with the structure

Complies

C.The IR spectrum of sample should be identical with that of reference standard;

Complies

D.HPLC-ESI-MS

The retention time of the major peak in the chromatogram of the Assay preparation corresponds to that in the chromatogram of the Standard preparation, as obtained in the Assay.

Complies

Crystallinity

meets the requirements.

Complies

Loss on drying

≤2.0%

0.19%

Heavy metals

≤10 ppm

<10ppm

Water

≤1.0%

0.1%

Sulphated ash

≤0.5%, determined on 1.0 g.

0.009%

Related substances

Unspecified impurities: for each impurity

≤0.10%

<0.10%

Total Impurity

≤0.5%

0.18%

Purity

≥99.0%

99.7%

Assay

99.0%~101.0% (anhydrous substance).

99.8%

Microbiological Analysis

Total plate count

≤1000cfu/g

Complies

Yeast and Moulds

≤100cfu/g

Complies

E. Coli.

Absent

Negative

Salmonella

Absent

Negative

S.aureus

Absent

Negative

Storage

Preserve in well-closed, light-resistant and airtight containers.

Complies

 

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