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Home > Products >  High quality USP 39/EP 9.0 /BP 2012 GMP DMF FDA Dolasetron Mesylate Dalasetron Mesylate hydrate CAS NO 878143-33-0 producer

High quality USP 39/EP 9.0 /BP 2012 GMP DMF FDA Dolasetron Mesylate Dalasetron Mesylate hydrate CAS NO 878143-33-0 producer CAS NO.878143-33-0

  • Min.Order: 1 Gram
  • Payment Terms: T/T
  • Product Details

Keywords

  • Dalasetron (Mesylate hydrate)
  • 878143-33-0
  • cas 878143-33-0

Quick Details

  • ProName: High quality USP 39/EP 9.0 /BP 2012 GM...
  • CasNo: 878143-33-0
  • Molecular Formula: C19H20N2O3.CH4O3S.H2O
  • Appearance: white poeder
  • Application: pharmaceutical raw material
  • DeliveryTime: 3 days after the payment
  • PackAge: 25kgs packaging Fiber drum outside and...
  • Port: any China Port
  • ProductionCapacity: 1000 Kilogram/Month
  • Purity: 99%
  • Transportation: by air, sea and express
  • LimitNum: 1 Gram

Superiority

Overview
Quick Details
CAS No.:
878143-33-0
Other Names:
Dalasetron (Mesylate hydrate)
MF:
C19H20N2O3.CH4O3S.H2O
EINECS No.:
878143-33-0
Place of Origin:
Shanghai, China (Mainland)
Type:
Antibiotic and Antimicrobial Agents
Grade Standard:
Medicine Grade
Brand Name:
Dideu
Model Number:
USP 39
Purity:
99.9%
Test Standard:
EP 9.0/USP39/BP2015
Content:
99.0% to 101.0%
Test method:
HPLC-ESI-MS
Water:
0.5% Max.
Sulfated ash:
0.1% Max.
Heavy metals:
10ppm Max
Total Impurity:
0.5% Max.
Total plate count:
≤1000cfu/g
Yeast and Moulds:
≤100cfu/g
E. Coli.:
Absent

 

Details

Packaging & Delivery
Packaging Details:
25kgs/Drum; 5kgs/Tin&10kgs/Carton
Delivery Detail:
10 Days

   

Product Description

 

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

  Email:support(at)dideu.com(Skype), sales(at)dideu.com Telephone:+86-29-88380327

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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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