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Anagrelide

Anagrelide Impurities

Anagrelide is a phosphodiesterase inhibitor used primarily in the treatment of essential thrombocythemia to reduce platelet counts. Its impurity profile includes structurally related analogs, residual solvents, and degradation products formed under stress conditions such as hydrolysis, oxidation, and photolysis. Furthermore, typical degradation pathways involve oxidative modification of the quinazoline scaffold, hydrolytic cleavage of amide bonds, and rearrangement of substituents within the heteroaromatic framework. These impurities may affect the drug’s potency, stability, and safety. Importantly, all impurities are structurally characterized and qualified according to ICH guidelines for toxicological assessment and analytical validation.

Anagrelide EP Impurities

Pharmacopeial and non-pharmacopeial Anagrelide impurity compounds are available in compliance with European Pharmacopoeia (EP) specifications. These standards support analytical method development, impurity profiling, and long-term stability studies. In addition, EP traceable materials are supplied with validated analytical data, including purity, structural confirmation, and spectral characterization.

Anagrelide Related Compounds

Structurally related compounds and synthetic analogs associated with Anagrelide are included for impurity identification, toxicological qualification, and regulatory submission. Consequently, these related substances are used in forced degradation studies, genotoxicity assessments, and impurity threshold evaluations. They are essential for understanding the impurity profile and ensuring compliance with regulatory limits.

Anagrelide Impurity Reference Standards

Anagrelide impurity reference standards are provided with validated analytical data, including purity, NMR, MS, and full Certificates of Analysis. These standards are used in pharmaceutical research, method validation, and GMP-compliant quality control. Additionally, EP/USP traceable entries are available upon request and are routinely re-tested to ensure consistency and reliability.

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CAS No.

: 733043-41-9

Mol F.

: C10H7Cl2N3O2

Mol W.

: 272.1

Cat No.

: SA90301

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CAS No.

: 1092352-99-2

Mol F.

: C10H6Cl3N3O

Mol W.

: 290.5

Cat No.

: SA90304

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CAS No.

: 68475-42-3

Mol F.

: C10H7Cl2N3O

Mol W.

: 256.1

Cat No.

: SA90300

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CAS No.

: 444904-63-6

Mol F.

: C8H7Cl2N3

Mol W.

: 216.1

Cat No.

: SA90305

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CAS No.

: 183620-20-4

Mol F.

: C15H20Cl2N2O4

Mol W.

: 363.2

Cat No.

: SA90321

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CAS No.

: NA

Mol F.

: C11H11Cl2N3O2

Mol W.

: 288.1

Cat No.

: SA90319

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CAS No.

: NA

Mol F.

: C10H7Cl2N3O2

Mol W.

: 272.1

Cat No.

: SA90318

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CAS No.

: NA

Mol F.

: C11H11Cl2N3O5

Mol W.

: 336.1

Cat No.

: SA90306

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CAS No.

: 3065021-63-5

Mol F.

: C15H18Cl2N2O6

Mol W.

: 393.2

Cat No.

: SA90320

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CAS No.

: NA

Mol F.

: C10H7Cl2N3O2

Mol W.

: 272.1

Cat No.

: SA90317

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CAS No.

: 70380-52-8

Mol F.

: C11H11Cl2N3O2 : HBr

Mol W.

: 288.1 : 80.9

Cat No.

: SA90303

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CAS No.

: 2187431-30-5

Mol F.

: C11H11Cl3N2O4

Mol W.

: 341.6

Cat No.

: SA90311

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CAS No.

: 70406-92-7

Mol F.

: C11H14Cl2N2O2

Mol W.

: 277.2

Cat No.

: SA90308

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CAS No.

: 1159977-03-3

Mol F.

: C10H9Cl2N3O2

Mol W.

: 274.1

Cat No.

: SA90309

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CAS No.

: 742010-46-4

Mol F.

: C12H13Cl2N3O2

Mol W.

: 302.2

Cat No.

: SA90310

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CAS No.

: 349150-82-9

Mol F.

: C11H15ClN2O2

Mol W.

: 242.7

Cat No.

: SA90315

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CAS No.

: NA

Mol F.

: C11H14Cl2N2O2

Mol W.

: 277.1

Cat No.

: SA90316

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CAS No.

: 2187431-31-6

Mol F.

: C11H13Cl3N2O2

Mol W.

: 311.6

Cat No.

: SA90313

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CAS No.

: NA

Mol F.

: C11H13Cl2N3O3

Mol W.

: 306.1

Cat No.

: SA90307

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CAS No.

: 70380-54-0

Mol F.

: C11H11Cl2N3O2 : HCl

Mol W.

: 288.1 : 36.5

Cat No.

: SA90312

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CAS No.

: 85325-11-7

Mol F.

: C11H12Cl2N2O4

Mol W.

: 307.1

Cat No.

: SA90302

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CAS No.

: NA

Mol F.

: C11H14Cl2N2O2

Mol W.

: 277.1

Cat No.

: SA90314

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