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VAQORACHEMICALS
Impurity reference standards

Ibuprofen impurities & reference standards

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

87reference materials
4isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Ibuprofen
15687-27-1 · C13H18O2
View API
Reference Standard
(R)-Ibuprofen chemical structure
(R)-Ibuprofen
CAS
51146-57-7
Formula
C13H18O2
MW
206.28 g/mol
VQ-037625
Reference Standard
(R)-Ibuprofen-d3 chemical structure
(R)-Ibuprofen-d3
CAS
121702-86-1
Formula
C13H18O2
MW
209.3 g/mol
VQ-037640
Reference Standard
(S)-(+)-Ibuprofen chemical structure
(S)-(+)-Ibuprofen
CAS
51146-56-6
Formula
C13H18O2
MW
206.28 g/mol
VQ-037624
Reference Standard
(S)-Ibuprofen-d3 chemical structure
(S)-Ibuprofen-d3
CAS
1329643-44-8
Formula
C13H18O2
MW
209.3 g/mol
VQ-037641
Reference Standard
2-Hydroxyibuprofen chemical structure
2-Hydroxyibuprofen
CAS
51146-55-5
Formula
C13H18O3
MW
222.28 g/mol
VQ-031131
Reference Standard
Hydroxy Ibuprofen chemical structure
Hydroxy Ibuprofen
CAS
53949-54-5
Formula
C13H18O3
MW
222.28 g/mol
VQ-037632
Reference Standard
Ibufenac chemical structure
Ibufenac
CAS
1553-60-2
Formula
C12H16O2
MW
192.25 g/mol
VQ-037634
IP/BP/USP
Ibuprofen chemical structure
Ibuprofen
CAS
15687-27-1
Formula
C13H18O2
MW
206.28 g/mol
VQ-004003
Reference Standard
Ibuprofen 13C,d3 chemical structure
Ibuprofen 13C,d3
CAS
1261394-40-4
Formula
C13H18O2
MW
210.29 g/mol
VQ-037642
Reference Standard
Ibuprofen Arginine chemical structure
Ibuprofen Arginine
CAS
57469-82-6
Formula
C19H32N4O4
MW
380.5 g/mol
VQ-037637

FAQs — Ibuprofen impurities

Which Ibuprofen impurities do you supply?

We list 87 Ibuprofen-related reference materials, including process impurities, degradation products, 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 Ibuprofen 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 Ibuprofen 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 Ibuprofen impurity standards

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