(2-Amino-5,6-dichloroquinazolin-3(4H)-yl)acetic Acid
- CAS
- 1159977-03-3
- Formula
- C10H9Cl2N3O2
- MW
- 274.1 g/mol
VQ-020808
Impurity reference standards
Anagrelide impurities & reference standards
Characterised Anagrelide impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
34reference materials
1isotope-labelled
COAHPLC · NMR · MS on request
2-((2,3,4-Trichloro-6-nitrobenzyl)amino)acetic acid ethyl ester
- CAS
- 2187431-30-5
- Formula
- C13H12N2Na2O14S2
- MW
- 530.4 g/mol
VQ-024292
2-Amino-5,6-dichloro-3(4H)-quinazoline Acetic Acid Ethyl Ester Hydrobromide
- CAS
- 70381-75-8
- Formula
- C12H14BrCl2N3O2
- MW
- 383.07 g/mol
VQ-021591
2-Amino-5,6-dichloro-3(4H)-quinazoline Acetic Acid Hydrobromide
- CAS
- 1194434-39-3
- Formula
- C10H10BrCl2N3O2
- MW
- 355.01 g/mol
VQ-024294
2-Amino-5,6-dichloro-3(4H)-quinazolineacetic Acid Methyl Ester Monohydrobromide
- CAS
- 70380-52-8
- Formula
- C11H12BrCl2N3O2
- MW
- 369.04 g/mol
VQ-034995
Anagrelide Related Compound B Hydrochloride
- CAS
- 2203514-95-6
- Formula
- C10H10Cl3N3O2
- MW
- 310.6 g/mol
VQ-029158
Anagrelide USP Related compound A Hydrochloride
- CAS
- 2512201-53-3
- Formula
- C11H15Cl3N2O2
- MW
- 313.6 g/mol
VQ-035728
Ethyl (6-amino-2,3,4-trichlorobenzyl)glycinate
- CAS
- 2187431-31-6
- Formula
- C11H13Cl3N2O2
- MW
- 311.6 g/mol
VQ-021593
Ethyl 2-(6-amino-2,3-dichlorobenzylamino)acetate
- CAS
- 70406-92-7
- Formula
- C11H14Cl2N2O2
- MW
- 277.14 g/mol
VQ-021592
Ethyl-2-(6-amino-2,3-dichlorobenzylamino)acetate Hydrochloride
- CAS
- 85325-12-8
- Formula
- C11H15Cl3N2O2
- MW
- 313.6 g/mol
VQ-024293
Methyl 2-(2-amino-5,6-dichloroquinazolin-3(4H)-yl)acetate hydrochloride
- CAS
- 70380-54-0
- Formula
- C11H11Cl2N3O2 : HCl
- MW
- 324.59 g/mol
VQ-024297
FAQs — Anagrelide impurities
Which Anagrelide impurities do you supply?
We list 34 Anagrelide-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 Anagrelide 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 Anagrelide 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 Anagrelide impurity standards
We reply within one business day with price, pack options, lead time and documentation.