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

Cholesterol impurities & reference standards

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

45reference materials
3isotope-labelled
COAHPLC · NMR · MS on request
Reference Standard
24-Ketocholesterol chemical structure
24-Ketocholesterol
CAS
17752-16-8
Formula
C27H44O2
MW
400.6 g/mol
VQ-044406
Reference Standard
7-Keto Cholesterol chemical structure
7-Keto Cholesterol
CAS
566-28-9
Formula
C27H44O2
MW
400.6 g/mol
VQ-021147
Cholestenone chemical structure
Cholestenone
CAS
601-57-0
Formula
C27H44O
MW
384.6 g/mol
VQ-047780
Reference Standard
Cholesterol-d7 chemical structure
Cholesterol-d7
CAS
83199-47-7
Formula
C27H46O
MW
393.7 g/mol
VQ-043392
Reference Standard
Doristerol chemical structure
Doristerol
CAS
566-99-4
Formula
C27H46O
MW
386.7 g/mol
VQ-036282
Reference Standard
Epicholesterol chemical structure
Epicholesterol
CAS
474-77-1
Formula
C27H46O
MW
386.7 g/mol
VQ-032779
Reference Standard
Triflumuron chemical structure
Triflumuron
CAS
64628-44-0
Formula
C15H10ClF3N2O3
MW
358.7 g/mol
VQ-029778
Reference Standard
Zymosterol chemical structure
Zymosterol
CAS
128-33-6
Formula
C27H44O
MW
384.6 g/mol
VQ-036283
Reference Standard
β-Cholestanol chemical structure
β-Cholestanol
CAS
80-97-7
Formula
C27H48O
MW
388.7 g/mol
VQ-024953

FAQs — Cholesterol impurities

Which Cholesterol impurities do you supply?

We list 45 Cholesterol-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 Cholesterol 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 Cholesterol 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 Cholesterol 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.