Worldwide shipping · 120+ destinationsCOA & GHS SDS with every lotMon–Sat, 09:30–18:30 IST
VAQORACHEMICALS
Impurity reference standards

Amlodipine impurities & reference standards

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

86reference materials
1nitrosamine impurities
3isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Amlodipine
88150-42-9 · C20H25ClN2O5
View API
Reference Standard
Amlodipine orotate chemical structure
Amlodipine orotate
CAS
914941-70-1
Formula
C25H29ClN4O9
MW
565 g/mol
VQ-035695
Reference Standard
Amlodipine WS chemical structure
Amlodipine WS
CAS
88150-42-9
Formula
C20H25ClN2O5
MW
408.9 g/mol
VQ-007312
Reference Standard
Amlodipine-d4 chemical structure
Amlodipine-d4
CAS
1185246-14-3
Formula
C20H25ClN2O5
MW
412.9 g/mol
VQ-029137
Reference Standard
Desethyl Amlodipine chemical structure
Desethyl Amlodipine
CAS
1809326-44-0
Formula
C18H21ClN2O5
MW
380.8 g/mol
VQ-021562
Reference Standard
N-Formyl Amlodipine chemical structure
N-Formyl Amlodipine
CAS
93848-81-8
Formula
C21H25ClN2O6
MW
436.9 g/mol
VQ-021563
Reference Standard
N-Nitroso Amlodipine chemical structure
N-Nitroso Amlodipine
CAS
3048033-49-1
Formula
C20H24ClN3O6
MW
437.9 g/mol
VQ-029131
Reference Standard
R-Amlodipine chemical structure
R-Amlodipine
CAS
103129-81-3
Formula
C20H25ClN2O5
MW
408.9 g/mol
VQ-024254
Reference Standard
R-Amlodipine-d4 chemical structure
R-Amlodipine-d4
CAS
1346616-97-4
Formula
C20H25ClN2O5
MW
412.9 g/mol
VQ-035706

FAQs — Amlodipine impurities

Which Amlodipine impurities do you supply?

We list 86 Amlodipine-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 Amlodipine 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 Amlodipine 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 Amlodipine impurity standards

We reply within one business day with price, pack options, lead time and documentation.

By submitting you agree to our privacy policy. We never share your details.