Checklist for Do’s and Don’ts for Using Glassware for Analysis

Checklist for Do’s and Don’ts for Using Glassware for Analysis

Checklist for Do’s

  • Use Class A Glassware for analysis
  • Use  transparent glassware for analysis
  • Before using glassware for analysis check for cracks or breakage.
  • Use exact capacity glassware by checking the marking of capacity e.g. ‘20’ flask not to be used for 25 ml capacity.
  • Check dilution marking of glassware for up-to-mark.
  • Use Dry & clean glassware for analysis
  • Check the free-flowing capacity of the pipette.
  • For titration use burette capacity such that the titrant volume is 30% of the nominal volume of the burette. e.g.: If titrant volume is in excess of 15 ml – use 50 ml burette. Less of 15 ml use 25 ml burette
  • Check to leak of solvent or titrant While using the separator for extraction and Burette for titration.
  • Use amber-colored glassware for analysis of light-sensitive material.
  • Use a pipette stand, separator stand, and test tube stands to avoid breakage.

Checklist for Do’s and Don’ts

  • Don’t use  Class B Glassware for analysis
  • Don’t use Opaque cloudy glassware for analysis
  • Don’t use cracked & broken glassware for analysis
  • Do not assume any capacity of glassware for usage.
  • Don’t use glassware without marking
  • Don’t use unclean glassware for analysis.
  • Do not use a pipette that gives adherence of solvent to the side walls of the pipette
  • For titration Don’t use a burette of nominal volume.
  • e.g.: If the titrant volume is in excess of 15 ml – don’t use a 20 ml burette. Less than 15 ml don’t use 10 ml burette.
  • Don’t use a leakage separator for extraction and a burette for titration
  • Don’t use routine glassware for analysis of light-sensitive material which may degrade the material.
  • Don’t keep pipettes, separators, and test tubes on the table.

About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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