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Granisetron

Granisetron Impurities

Granisetron is a selective 5‑HT₃ receptor antagonist used in the prevention of chemotherapy-induced and postoperative nausea and vomiting. 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 indazole 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.

Granisetron EP Impurities

Pharmacopeial and non-pharmacopeial Granisetron 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.

Granisetron Related Compounds

Structurally related compounds and synthetic analogs associated with Granisetron 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.

Granisetron Impurity Reference Standards

Granisetron 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.

: 133841-15-3

Mol F.

: C18H24N4O2

Mol W.

: 328.4

Cat No.

: SA90608

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CAS No.

: 109889-09-0

Mol F.

: C18H24N4O

Mol W.

: 312.4

Cat No.

: SA90600

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CAS No.

: 127472-42-8

Mol F.

: C18H24N4O

Mol W.

: 312.4

Cat No.

: SA90601

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CAS No.

: 107007-95-4

Mol F.

: C17H22N4O

Mol W.

: 298.4

Cat No.

: SA90602

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CAS No.

: 160177-67-3

Mol F.

: C17H22N4O

Mol W.

: 298.4

Cat No.

: SA90603

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CAS No.

: 50890-83-0

Mol F.

: C9H8N2O2

Mol W.

: 176.2

Cat No.

: SA90604

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CAS No.

: 76272-56-5

Mol F.

: C9H18N2

Mol W.

: 154.3

Cat No.

: SA90605

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CAS No.

: 1364914-39-5

Mol F.

: C18H24N4O

Mol W.

: 312.4

Cat No.

: SA90607

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CAS No.

: 34252-44-3

Mol F.

: C9H8N2O2

Mol W.

: 176.2

Cat No.

: SA90609

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CAS No.

: 4498-67-3

Mol F.

: C8H6N2O2

Mol W.

: 162.2

Cat No.

: SA90610

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CAS No.

: 1363173-34-5

Mol F.

: C18H14N4O3

Mol W.

: 334.3

Cat No.

: SA90606

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CAS No.

: NA

Mol F.

: C8H5N3O3

Mol W.

: 191.1

Cat No.

: SA90613

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CAS No.

: 98556-68-4

Mol F.

: C8H4N4O

Mol W.

: 172.1

Cat No.

: SA90612

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CAS No.

: NA

Mol F.

: C17H21N5O2

Mol W.

: 327.4

Cat No.

: SA90614

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CAS No.

: NA

Mol F.

: C17H21N5O2

Mol W.

: 327.4

Cat No.

: SA90611

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CAS No.

: NA

Mol F.

: C18H23N5O2

Mol W.

: 341.4

Cat No.

: SA90615

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