Impurity reference standards
Cobicistat impurities & reference standards
Characterised Cobicistat impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
24reference materials
COAHPLC · NMR · MS on request
(2R,5R)-1,6-Diphenylhexane-2,5-diamine Dihydrochloride
- CAS
- 1247119-31-8
- Formula
- C18H26Cl2N2
- MW
- 341.3 g/mol
In stock
(S)-(-)-Alpha-Amino-gamma-butyrolactone hydrobromide
- CAS
- 15295-77-9
- Formula
- C4H8BrNO2
- MW
- 182.02 g/mol
VQ-039325
(S)-1-((2-Isopropylthiazol-4-yl)methyl)-1-methyl-3-(2-oxotetrahydrofuran-3-yl)urea
- CAS
- 1004316-93-1
- Formula
- C13H19N3O3S
- MW
- 297.38 g/mol
VQ-029919
2-(4-((Methylamino)methyl)thiazol-2-yl)propan-2-ol
- CAS
- 1051463-24-1
- Formula
- C8H14N2OS
- MW
- 186.28 g/mol
VQ-029917
Cobicistat on Colloidal silicon Dioxide Related Compound 7
- CAS
- 1004316-56-6
- Formula
- C28H30N4O4S2
- MW
- 550.7 g/mol
In stock
Ethyl(S)-2-(3-((2-isopropylthiazol-4-yl)methyl)-3-methylureido)-4-morpholinobutanoate oxalate
- CAS
- 1247119-35-2
- Formula
- C19H32N4O4S
- MW
- 412.5 g/mol
VQ-029916
N-((2-Isopropylthiazol-4-yl)methyl)-N-methyl-1H-imidazole-1-carboxamide
- CAS
- 1247119-46-5
- Formula
- C12H16N4OS
- MW
- 264.35 g/mol
VQ-036431
Thiazol-5-Ylmethyl ((2R,5R)-5-((S)-2-Amino-4-morpholinobutanamido)-1,6-diphenylhexan-2-yl)Carbamate
- CAS
- 1051463-15-0
- Formula
- C31H41N5O4S
- MW
- 579.8 g/mol
VQ-029920
Thiazol-5-ylmethyl ((2S,5S)-5-((S)-2-(3-((2-isopropylthiazol-4-yl)methyl)-3-methylureido)-4-morpholinobutanamido)-1,6-diphenylhexan-2-yl)carbamate
- CAS
- 2230789-82-7
- Formula
- C40H53N7O5S2
- MW
- 776 g/mol
VQ-025073
FAQs — Cobicistat impurities
Which Cobicistat impurities do you supply?
We list 24 Cobicistat-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 Cobicistat 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 Cobicistat 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 Cobicistat impurity standards
We reply within one business day with price, pack options, lead time and documentation.