Impurity reference standards
Bupivacaine impurities & reference standards
Characterised Bupivacaine impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
26reference materials
1nitrosamine impurities
3isotope-labelled
COAHPLC · NMR · MS on request
1-Butyl-N-(2,4-dimethylphenyl)piperidine-2-carboxamide
- CAS
- 2774312-11-5
- Formula
- C18H28N2O
- MW
- 288.4 g/mol
VQ-024686
N-(2,6-Dimethylphenyl)-1-nitrosopiperidine-2-carboxamide
- CAS
- 3035512-94-5
- Formula
- C14H19N3O2
- MW
- 261.32 g/mol
VQ-044483
FAQs — Bupivacaine impurities
Which Bupivacaine impurities do you supply?
We list 26 Bupivacaine-related reference materials, including process impurities, degradation products, nitrosamine impurities, stable-isotope-labelled standards and related compounds. Each is supplied with a COA, and characterisation data (HPLC, 1H-NMR, MS, IR) can be provided on request.
What are Bupivacaine impurity standards used for?
They are used for analytical method development and validation, impurity identification and quantification, forced-degradation and stability studies, and to support ANDA, DMF and other regulatory submissions under ICH Q3A/Q3B (and ICH M7 for mutagenic impurities).
Can you synthesise a Bupivacaine impurity that is not listed?
Yes. Our custom synthesis service can prepare and characterise unlisted impurities, metabolites and labelled analogues from milligram to gram scale. Share the structure or name and required quantity for a quotation.
Request Bupivacaine impurity standards
We reply within one business day with price, pack options, lead time and documentation.