1,2-Distearoyl-sn-glycero-3-phospho-rac-(1-glycerol) Sodium Salt
- CAS
- 200880-42-8
- Formula
- C42H82NaO10P
- MW
- 801.1 g/mol
VQ-036821
Impurity reference standards
Doxorubicin impurities & reference standards
Characterised Doxorubicin impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
21reference materials
COAHPLC · NMR · MS on request
6,11-Dihydroxy-8-(2-hydroxyacetyl)-1-methoxytetracene-5,12-dione
- CAS
- 105612-58-6
- Formula
- C21H14O7
- MW
- 378.3 g/mol
VQ-030091
FAQs — Doxorubicin impurities
Which Doxorubicin impurities do you supply?
We list 21 Doxorubicin-related reference materials, including process impurities, degradation products and related compounds. Each is supplied with a COA, and characterisation data (HPLC, 1H-NMR, MS, IR) can be provided on request.
What are Doxorubicin 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 Doxorubicin 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 Doxorubicin impurity standards
We reply within one business day with price, pack options, lead time and documentation.