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VAQORACHEMICALS
Impurity reference standards

Ledipasvir impurities & reference standards

Characterised Ledipasvir impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.

13reference materials
COAHPLC · NMR · MS on request
Reference Standard
Ledipasvir chemical structure
Ledipasvir
CAS
1256388-51-8
Formula
C49H54F2N8O6
MW
889 g/mol
VQ-031458
Reference Standard
Ledipasvir Acetone chemical structure
Ledipasvir Acetone
CAS
1441674-54-9
Formula
C52H60F2N8O7
MW
947.1 g/mol
VQ-048811
Reference Standard
Methyl
Methyl
CAS
2040487-43-0
Formula
C49H54N8O7
MW
867.02 g/mol
VQ-034967
Reference Standard
Methyl chemical structure
Methyl
CAS
1256393-35-7
Formula
C49H54F2N8O6
MW
889 g/mol
VQ-043765
Reference Standard
Methyl chemical structure
Methyl
CAS
1256391-66-8
Formula
C49H54F2N8O6
MW
889 g/mol
VQ-043766

FAQs — Ledipasvir impurities

Which Ledipasvir impurities do you supply?

We list 13 Ledipasvir-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 Ledipasvir 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 Ledipasvir 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 Ledipasvir impurity standards

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