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N-Nitroso Diisopropylamine (NDIPA)
N-Nitroso Diisopropylamine (NDIPA)
N-Nitroso Diisopropylamine (NDIPA)
N-Nitroso Diisopropylamine (NDIPA)
N-Nitroso Diisopropylamine (NDIPA)
N-Nitroso Diisopropylamine (NDIPA)

N-Nitroso Diisopropylamine (NDIPA)

Price 1700 INR/ Kilograms

MOQ : 25 Kilograms

N-Nitroso Diisopropylamine (NDIPA) Specification

  • Molecular Weight
  • 130.19 g/mol Grams (g)
  • Shelf Life
  • 24-36 Months
  • Ph Level
  • 6.0 7.0
  • Taste
  • Other
  • Structural Formula
  • [(CH)CH]N-N=O
  • HS Code
  • 292990
  • Melting Point
  • 46C to 49C
  • Boiling point
  • 194.5C at 760 mmHg
  • EINECS No
  • 210-001-4
  • Solubility
  • Highly soluble in Methanol, Acetonitrile, and Chloroform
  • Loss on Drying
  • 0.5%
  • Smell
  • Other
  • Particle Size
  • Standard Fine Powder/Crystals
  • Heavy Metal (%)
  • 0.001%
  • Storage
  • Freezer
  • Molecular Formula
  • CHNO
  • Medicine Name
  • N-Nitroso Diisopropylamine (NDIPA) Reference Standard
  • Chemical Name
  • N-Nitrosodiisopropylamine
  • CAS No
  • 601-77-4
  • Type
  • Pharmaceutical Intermediates
  • Grade
  • Other
  • Usage
  • Laboratory research, drug impurity profiling, HPLC-MS/MS testing calibration
  • Purity(%)
  • 98.0%
  • Appearance
  • Crystalline solid
  • Physical Form
  • Solid
 

N-Nitroso Diisopropylamine (NDIPA) Trade Information

  • Minimum Order Quantity
  • 25 Kilograms
  • Payment Terms
  • Cash in Advance (CID)
  • Supply Ability
  • 500 Kilograms Per Month
  • Delivery Time
  • 1 Week
  • Sample Available
  • Yes
  • Sample Policy
  • Contact us for information regarding our sample policy
  • Packaging Details
  • Amber glass vials (1 mL, 10 mg, or 50 mg), packed under inert gas (nitrogen/argon), sealed in thermocol boxes with ice packs.
  • Main Domestic Market
  • All India
  • Certifications
  • coa,msds
 

N-Nitroso Diisopropylamine (NDIPA) About

N-Nitroso Diisopropylamine (NDIPA) is a chemical compound belonging to the nitrosamine class, recognized globally as a potential mutagenic impurity and suspected carcinogen in pharmaceutical products. It gained significant regulatory attention following the discovery of nitrosamine impurities in widely prescribed medications like sartan-based blood pressure drugs. 


  • Pharmaceutical Reference Standards: It serves as a Certified Reference Material (CRM) to test and quantify impurities in drug batches. Chemists use it to ensure compliance with threshold limits set by international regulators. 
  • Analytical Testing Methods: Labs utilize NDIPA standards to develop and validate high-sensitivity testing methods. These typically include High-Performance Liquid Chromatography-Tandem Mass Spectrometry (HPLC-MS/MS) and Gas Chromatography.
  • Toxicology and Mutagenicity Studies: Researchers study NDIPA to map the metabolic pathways and structural risk factors of nitrosamines. For instance, toxicological assessments show it has lower mutagenicity compared to nitrosamines with more -hydrogen atoms, helping refine structural risk modeling.

 

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