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VAQORACHEMICALS
Impurity reference standards

Lanreotide impurities & reference standards

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

7reference materials
COAHPLC · NMR · MS on request
Reference Standard
D-Cys(7)-Lanreotide
D-Cys(7)-Lanreotide
CAS
205234-53-3
Formula
C54H69N11O10S2
MW
1096.32 g/mol
VQ-031435
Reference Standard
L-Nal-Lanreotide
L-Nal-Lanreotide
CAS
205234-49-7
Formula
C54H69N11O10S2
MW
1096.3 g/mol
VQ-031433
Reference Standard
L-Trp4-Lanreotide
L-Trp4-Lanreotide
CAS
1219612-61-9
Formula
C54H69N11O10S2
MW
1096.33 g/mol
VQ-031436
Reference Standard
Lanreotide Acetate chemical structure
Lanreotide Acetate
CAS
127984-74-1
Formula
C56H73N11O12S2
MW
1156.4 g/mol
VQ-043201
Reference Standard
Lys-(Ac)5 Lanreotide
Lys-(Ac)5 Lanreotide
CAS
1353092-24-6
Formula
C56H71N11O11S2
MW
1138.36 g/mol
VQ-026353
Reference Standard
N-Ac-Lanreotide
N-Ac-Lanreotide
CAS
109605-17-6
Formula
C56H71N11O11S2
MW
1138.36 g/mol
VQ-026352

FAQs — Lanreotide impurities

Which Lanreotide impurities do you supply?

We list 7 Lanreotide-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 Lanreotide 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 Lanreotide 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 Lanreotide impurity standards

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

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