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| Product | Description | |
|---|---|---|
| Zolpidem Impurity 69 | Zolpidem Impurity 69. Uses: For analytical and research use. CAS No. 109461-69-0. Molecular formula: C17H16N2O2. Mole weight: 280.33. Catalog: APB109461690. |  |
| Zolpidem Impurity 71 | Zolpidem Impurity 71. Uses: For analytical and research use. CAS No. 917252-78-9. Molecular formula: C16H14N2O2. Mole weight: 266.3. Catalog: APB917252789. | |
| Zolpidem Impurity 72 | Zolpidem Impurity 72. Uses: For analytical and research use. CAS No. 917252-80-3. Molecular formula: C18H16N2O4. Mole weight: 324.34. Catalog: APB917252803. | |
| Zolpidem Impurity 73 | Zolpidem Impurity 73. Uses: For analytical and research use. CAS No. 1330277-06-9. Molecular formula: C14H8D6N2O. Mole weight: 232.32. Catalog: APB1330277069. | |
| Zolpidem Impurity 76 (Sulbenox) | Zolpidem Impurity 76 (Sulbenox). Uses: For analytical and research use. CAS No. 58095-31-1. Molecular formula: C9H10N2O2S. Mole weight: 210.25. Catalog: APB58095311. | |
| Zolpidem Impurity 77 | Zolpidem Impurity 77. Uses: For analytical and research use. CAS No. 20972-36-5. Molecular formula: C11H10O3. Mole weight: 190.2. Catalog: APB20972365. | |
| Zolpidem Tartrate CEP | Zolpidem Tartrate CEP. CAS No. 99294-93-6. Cenik is your partner of choice for specialised chemicals. We don't just provide products - we supply solutions to your technical and regulatory specifications. |  |
| Zolpidem Tartrate Impurity 18 | Zolpidem Tartrate Impurity 18. Uses: For analytical and research use. CAS No. 118026-15-6. Molecular formula: C19H21Cl2N3O. Mole weight: 378.3. Catalog: APB118026156. | |
| Zolpidem USP Related Compound C | Zolpidem USP Related Compound C. Uses: For analytical and research use. CAS No. 14547-80-9. Molecular formula: C13H12N2O. Mole weight: 212.25. Catalog: APB14547809. | |
| Zolucatetide | Zolucatetide (FOG-001;I-66) is a potent β-catenin inhibitor with an IC50 of <50 nM. Zolucatetide can inhibits β-catenin and T-cell factor (TCF) transcription factor interaction. Zolucatetide inhibits cell proliferation and induces cell cycle arrest in target cells. Zolucatetide exhibits anti-tumor efficacy in mice bearing COLO320DM colon cancer cell (with APC, TP53 mutations) xenografts. Zolucatetide can be used for the study of colon cancer[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: FOG-001; I-66. CAS No. 3044032-95-0. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P10925. |  |
| Zomepirac Sodium Salt | Zomepirac is an analgesic, anti-inflammatory drug. Group: Biochemicals. Alternative Names: 5-(4-Chlorobenzoyl)-1,4-dimethyl-1H-pyrrole-2-acetic Acid Sodium Salt; McN 2783-21-98; Sodium Zomepirac; Zomax; Zomepirac Sodium; Zomepirac Sodium Salt. Grades: Highly Purified. CAS No. 64092-48-4. Pack Sizes: 100mg. US Biological Life Sciences. |  Worldwide |
| Zomiradomide | Zomiradomide is an orally active PROTAC degrader for IRAK4 (DC50=6 nM), thereby inhibiting the NF-κB signaling pathway. Zomiradomide acts also as a molecular glue, recruiting Ikaros and Aiolos, and mediating their degradation (DC50 for Ikaros is 1 nM), thereby activating the type I IFN signaling pathway[1][2][3]. (Pink: target protein ligand PROTAC IRAK4 ligand-5 (HY-168311), Blue: E3 ligase ligand Thalidomide-4-Br (HY-W039116), Black: linker (HY-168313)). Uses: Scientific research. Category: Signaling pathways. Alternative Names: KT-413. CAS No. 2655656-99-6. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-153368. | |
| Zomitriptan EP impurity A | Zomitriptan EP impurity A. Uses: For analytical and research use. CAS No. 139264-24-7. Molecular formula: C16H21N3O2. Mole weight: 287.36. Catalog: APB139264247. | |
| Zomitriptan EP impurity B | Zomitriptan EP impurity B. Uses: For analytical and research use. CAS No. 251451-30-6. Molecular formula: C16H21N3O3. Mole weight: 303.36. Catalog: APB251451306. | |
| Zomitriptan EP impurity C | Zomitriptan EP impurity C. Uses: For analytical and research use. CAS No. 1350928-05-0. Molecular formula: C38H53N7O4. Mole weight: 671.89. Catalog: APB1350928050. | |
| Zomitriptan EP impurity D | Zomitriptan EP impurity D. Uses: For analytical and research use. CAS No. 139264-15-6. Molecular formula: C14H17N3O2. Mole weight: 259.31. Catalog: APB139264156. | |
| Zomitriptan EP impurity E | Zomitriptan EP impurity E. Uses: For analytical and research use. CAS No. 152305-23-2. Molecular formula: C10H12N2O2. Mole weight: 192.22. Catalog: APB152305232. | |
| Zomitriptan EP impurity F | Zomitriptan EP impurity F. Uses: For analytical and research use. CAS No. 139264-69-0. Molecular formula: C15H23N3O. Mole weight: 261.37. Catalog: APB139264690. | |
| Zomitriptan EP impurity G | Zomitriptan EP impurity G. Uses: For analytical and research use. CAS No. 139264-35-0. Molecular formula: C15H19N3O2. Mole weight: 273.34. Catalog: APB139264350. | |
| Zomitriptan EP impurity H | Zomitriptan EP impurity H. Uses: For analytical and research use. CAS No. 2518343-21-8. Molecular formula: C16H19N3O2. Mole weight: 285.35. Catalog: APB2518343218. | |
| Zomitriptan EP impurity I | Zomitriptan EP impurity I. Uses: For analytical and research use. CAS No. 659738-69-9. Molecular formula: C17H21N3O4. Mole weight: 331.37. Catalog: APB659738699. | |
| ZONATAC NG 98 | ZONATAC NG 98. |  |
| Zongertinib | Zongertinib (BI 1810631) is a potent and selective HER2 and EGFR tyrosine kinase inhibitor with IC50 values of 13 nM and 579 nM, respectively. Zongertinib has antitumor activity and can be used in the study of multiple solid tumors[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: BI 1810631. CAS No. 2728667-27-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148810. | |
| Zoniporide Hydrochloride | Zoniporide is a potent and selective inhibitor of human sodium-hydrogen exchanger isoform1(NHE-1) and protects against cardiac ischemia-reperfusion injury. Group: Biochemicals. Alternative Names: N-(Aminoiminomethyl)-5-cyclopropyl-1-(5-quinolinyl)-1H-pyrazole-4-carboxamide Hydrochloride;CP 597396 Hydrochloride; N-[5-Cyclopropyl-1-(quinolin-5-yl)-1H-pyrazole-4-carbonyl]guanidine Hydrochloride; [1-(Quinolin-5-yl)-5-cyclopropyl-1H-pyrazole-4-carbonyl]guanidine Hydrochloride. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Zonisamide | Zonisamide. Group: Biochemicals. Grades: Highly Purified. CAS No. 68291-97-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Zonisamide | Zonisamide (AD 810) is an orally active carbonic anhydrase inhibitor, with Kis of 35.2 and 20.6 nM for hCA II and hCA V, respectively. Zonisamide exerts neuroprotective effects through anti-apoptosis and upregulating MnSOD levels. Zonisamide also increases the expression of Hrd1, thereby improving cardiac function in AAC rats. Zonisamide can be used in studies of seizure, parkinsons disease and cardiac hypertrophy[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AD 810; CI 912. CAS No. 68291-97-4. Pack Sizes: 10 mM * 1 mL in DMSO; 200 mg; 500 mg. Product ID: HY-B0124. | |
| Zonisamide (1,2-Benzisoxazole-3-methanesulfonamide) | Heterocyclic methanesulfonide with anticonvulsant properties. The compound is under investigation for potential therapeutic use as an antiepileptic drug. Group: Biochemicals. Alternative Names: 1,2-Benzisoxazole-3-methanesulfonamide. Grades: Highly Purified. CAS No. 68291-97-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Zonisamide-[13C2,15N] | Zonisamide-[13C2,15N] is the labelled analogue of Zonisamide, which is a Sulfonamide-derived antiseizure agent and coule be used as a neuroprotective as well as neuroresearch agent. Synonyms: Zonisamide 13C2 15N; 1,2-Benzisoxazole-13C2-3-methanesulfonamide-15N; 3-(Sulfamoyl-15N-methyl)-1,2-benzisoxazole-13C2. Grade: 95% by HPLC; 98% atom 13C; 98% atom 15N. CAS No. 1188265-58-8. Molecular formula: C6[13C]2H8N[15N]O3S. Mole weight: 215.20. |  |
| Zonisamide-[13C6] | An isotope labelled Zonisamide. Zonisamide can be used to treat the symptoms of epilepsy and Parkinson's disease. Grade: 95% by HPLC; 98% atom 13C. CAS No. 1435934-68-1. Molecular formula: C2[13C]6H8N2O3S. Mole weight: 218.18. | |
| Zonisamide-[d4] | An isotope labelled Zonisamide. Zonisamide can be used to treat the symptoms of epilepsy and Parkinson's disease. Uses: Labelled sulfonamide antiseizure agent; blocks repetitive firing of voltagesensitive sodium channels and reduces voltage-sensitive t-type calcium currents. heterocyclic methanesulfonide with anticonvulsant properties. the compound is under investigation f. Synonyms: Zonisamide D4. Grade: 95% atom D. CAS No. 1020720-04-0. Molecular formula: C8H4D4N2O3S. Mole weight: 216.25. | |
| Zonisamide-d4 (1,2-Benzisoxazole-3-methanesulfonamide-d4) | A deuterated heterocyclic methanesulfonide with anticonvulsant properties. The compound is under investigation for potential therapeutic use as an antiepileptic drug. Group: Biochemicals. Alternative Names: 1,2-Benzisoxazole-3-methanesulfonamide-d4. Grades: Highly Purified. CAS No. 1020720-04-0. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Zonisamide Impurity 1 | Zonisamide Impurity 1. Uses: For analytical and research use. CAS No. 4865-84-3. Molecular formula: C9H7NO3. Mole weight: 177.2. Catalog: APB4865843-1. | |
| Zonisamide Impurity 2 | Zonisamide Impurity 2. Uses: For analytical and research use. Molecular formula: C9H9NO4S. Mole weight: 227.2. Catalog: APB000065. | |
| Zonisamide Impurity 3 | Zonisamide Impurity 3. Uses: For analytical and research use. CAS No. 73101-65-2. Molecular formula: C8H6ClNO3S. Mole weight: 231.7. Catalog: APB73101652. | |
| Zonisamide-N-(6-hexanoic Acid) | Zonisamide derivative. Group: Biochemicals. Alternative Names: ZNS Carboxylic Acid; 6- [ [ (1, 2-Benzisoxazol-3-ylmethyl) sulfonyl] amino] hexanoic Acid. Grades: Highly Purified. CAS No. 1076199-51-3. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Zonisamide N,N-Dimethylformimidamide | Zonisamide related compound C. Group: Biochemicals. Alternative Names: (N)-Benzisox-3-ylmethylsulfonyl)-N,N-dimethylformimidamide. Grades: Highly Purified. CAS No. 1217201-89-2. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Zonisamide Related Compound A | Zonisamide Related Compound A. Uses: For analytical and research use. CAS No. 73101-64-1. Mole weight: 235.19. Catalog: AP73101641. | |
| Zonisamide Related Compound C | Zonisamide Related Compound C. Uses: For analytical and research use. CAS No. 1217201-89-2. Mole weight: 267.30. Catalog: AP1217201892. | |
| Z-Onsu | Z-Onsu. Group: Biochemicals. Alternative Names: N-Benzyl oxycarbonyl oxysuccinimide . Grades: Highly Purified. CAS No. 13139-17-8. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C12H11NO5. US Biological Life Sciences. | Worldwide |
| ZONYL FS-300 | ZONYL FS-300 is a fluorosurfactant known for its ability to reduce liquid surface tension and provide unique properties such as excellent wetting, spreading and leveling capabilities. CAS No. 197664-69-0. Product ID: ACM197664690. Molecular formula: RfCH2CH2O(CH2CH2O)xH. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Zonyl FS-300 fluorosurfactant | Zonyl FS-300 fluorosurfactant. Alternative Names: ZONYL FS-300. CAS No. 197664-69-0. Purity: 25%. Product ID: ACM197664690-1. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Zopiclone | Cyclopyrrolone member of a family of non-benzodiazepine GABAA receptor agonists. This is a controlled substance (depressant) in the US but not in Canada. Sedative, hypnotic. Group: Biochemicals. Alternative Names: 4-Methyl-1-piperazine-carboxylic Acid 6-(5-chloro-2-pyridinyl)-6,7-dihydro-7-oxo-5H-pyrrolo[3,4-b]pyrazin-5-yl Ester; RP-27267; Amoban; Imovane; Limovan; Sopivan; Ximovan; Zimovane. Grades: Highly Purified. CAS No. 43200-80-2. Pack Sizes: 10mg, 25mg, 50mg, 100mg. Molecular Formula: C17H17ClN6O3. US Biological Life Sciences. | Worldwide |
| Zopiclone-d8 | Cyclopyrrolone member of a family of non-benzodiazepine GABAA receptor agonists. This is a controlled substance (depressant) in the US but not in Canada. Sedative, hypnotic. Group: Biochemicals. Alternative Names: 4-Methyl-1-piperazine-d8-carboxylic Acid 6-(5-chloro-2-pyridinyl)-6,7-dihydro-7-oxo-5H-pyrrolo[3,4-b]pyrazin-5-yl Ester; RP-27267-d8; Amoban-d8; Imovane-d8; Limovan-d8; Sopivan-d8; Ximovan-d8; Zimovane. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Zopiclone-d8 N-Oxide. (Mixture of diastereomers) (1-Piperazine-d8-carboxylic Acid 4-Methyl-4-oxide 6-(5-Chloro-pyridin-2-yl)-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-5yl Ester,. RP 29753-d8) | A labeled metabolite of Zopiclone. Group: Biochemicals. Alternative Names: 1-Piperazine-d8-carboxylic Acid 4-Methyl-4-oxide 6-(5-Chloro-pyridin-2-yl)-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-5yl Ester;RP 29753-d8. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Zopiclone Impurity 15 | Zopiclone Impurity 15. Uses: For analytical and research use. CAS No. 4180-30-7. Molecular formula: C11H22N4O. Mole weight: 226.32. Catalog: APB4180307. | |
| Zopiclone Impurity 2 | Zopiclone Impurity 2. Uses: For analytical and research use. CAS No. 1122549-43-2. Molecular formula: C11H9ClN4O2. Mole weight: 264.67. Catalog: APB1122549432. | |
| Zopiclone N-Oxide (Eszopiclone Impurity A) | Eszopiclone impurity A. Group: Biochemicals. Alternative Names: 1-Piperazine-carboxylic Acid 4-Methyl-4-oxide 6-(5-Chloro-pyridin-2-yl)-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-5yl Ester;RP 29753; Eszopiclone Impurity A. Grades: Highly Purified. CAS No. 43200-96-0. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Zopolrestat | Zopolrestat (CP73850) is a potent, orally active aldose reductase (AR) inhibitor with an IC50 of 3.1 nM. Zopolrestat is used for the research of diabetic complications[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CP73850. CAS No. 110703-94-1. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-19687. | |
| Zoptarelin doxorubicin | Zoptarelin doxorubicin (AEZS-108; AN-152) is a hybrid anticancer agent, containing Zoptarelin and Doxorubicin. Zoptarelin doxorubicin has been used to research targeting tumors expressing LHRH receptors. Zoptarelin doxorubicin abolishes tumor progression and induces remarkable apoptosis in vitro[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AEZS-108; AN-152. CAS No. 139570-93-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-16532. | |
| Zorevunersen sodium | Zorevunersen sodium is an antisense oligonucleotide targeting the Scn1a gene based on TANGO technology. Zorevunersen sodium increases Scn1a mRNA transcripts and elevates the expression level of NaV1.1 protein. Zorevunersen sodium restores the excitability of PV interneurons, thereby reducing seizures and prolonging survival in mice. Zorevunersen sodium can be used for research on Dravet syndrome[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: STK-001 sodium. CAS No. 2415330-05-9. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148410A. | |
| Zorifertinib | Zorifertinib (AZD3759) is a potent, orally active, BBB-penetrant, EGFR inhibitor. At Km ATP concentrations, the IC50s are 0.3, 0.2, and 0.2 nM for EGFRwt, EGFRL858R, and EGFRexon 19Del, respectively. Zorifertinib induces cancer cell apoptosis. Zorifertinib has antitumor activity, and can be used for NSCLC, HCC etc. research[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AZD3759. CAS No. 1626387-80-1. Pack Sizes: 10 mM * 1 mL in DMSO; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-18750. | |
| Z-Orn-OH HCl | Z-Orn-OH HCl. Molecular formula: C13H18N2O4. Mole weight: 266.3. | |
| Z-Orn(Z)-ONP | Z-Orn(Z)-ONP. Grade: 98% (HPLC). Molecular formula: C27H27N3O8. Mole weight: 521.5. | |
| Zosuquidar | Zosuquidar (LY335979) is a P-glycoprotein (P-gp) inhibitor (Ki=59 nM). Zosuquidar shows anti-tumor activities, and can be used in acute myelogenous leukemia (AML) research[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: RS 33295-198; LY-335979. CAS No. 167354-41-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg. Product ID: HY-15255. | |
| Zosuquidar trihydrochloride | Zosuquidar (LY335979) trihydrochloride is a P-glycoprotein (P-gp) inhibitor (Ki=59 nM). Zosuquidar trihydrochloride shows anti-tumor activities, and can be used in acute myelogenous leukemia (AML) research[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: RS 33295-198 trihydrochloride; LY-335979 trihydrochloride. CAS No. 167465-36-3. Pack Sizes: 10 mM * 1 mL in Water; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-50671. | |
| Zosuquidar Trihydrochloride | Multi-drug resistance (MDR) modulator; selective inhibitor of P-glycoprotein (P-gp). Antineoplastic adjunct (chemosensitizer). Group: Biochemicals. Alternative Names: (α R) -4- [ (1aα , 6α , 10bα ) -1, 1-Difluoro-1, 1a, 6, 10b-tetrahydrodibenzo [a, e]cyclopropa [c]cyclohepten-6-yl]-α - [ (5-quinolinyloxy) methyl]-1-piperazineethanol Hydrochloride; Zosuquidar Hydrochloride. Grades: Highly Purified. CAS No. 167465-36-3. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Zosurabalpin | Zosurabalpin is a polypeptide antibiotic targeting LPS transporter (LptB2FGC complex), which can block the transport of LPS and lead to endotoxin accumulation in cells, and has shown excellent antibacterial activity against Carbapenem-resistant Acinetobacter baumanni (CRAB) [1] [2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Abx MCP; RG6006. CAS No. 2379336-76-0. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-147429. | |
| Zotarolimus | Zotarolimus (ABT-578) is a derivative of Rapamycin (HY-10219), with anti-proliferative activity. Zotarolimus is an immunosuppressant. Zotarolimus is developed specifically for local delivery from stents for the prevention of coronary artery restenosis[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: ABT-578; A 179578. CAS No. 221877-54-9. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-12424. | |
| Zotarolimus | Zotarolimus (also known as ABT-578) is an analogue of rapamycin (sirolimus) that was designed to have a shorter in vivo half-life than rapamycin. Zotarolimus was found to be comparable in potency for inhibiting in vitro proliferation of both rat and human T cells and mechanistically similar to sirolimus in having high-affinity binding to the immunophilin FKBP12. Zotarolimus is a semi-synthetic derivative of rapamycin. It was designed for use in stents with phosphorylcholine as a carrier. Group: Biochemicals. Alternative Names: 40-epi-(N1-Tetrazolyl)-rapamycin; ABT-578; KY 12420. Grades: Highly Purified. CAS No. 221877-54-9. Pack Sizes: 1mg, 5mg. US Biological Life Sciences. | Worldwide |
| Zotarolimus | Zotarolimus (INN, codenamed ABT-578) is an immunosuppressant. It is a semi-synthetic derivative of rapamycin. It was designed for use in stents with phosphorylcholine as a carrier. Coronary stents reduce early complications and improve late clinical outcomes in patients needing interventional cardiology. Synonyms: A-179578; A 179578; A179578; ABT-578; ABT578; ABT 578. Grade: >98%. CAS No. 221877-54-9. Molecular formula: C52H79N5O12. Mole weight: 966.21. | |
| Zotatifin | Zotatifin (eFT226) is a potent, selective, and well-tolerated eIF4A inhibitor. Zotatifin promotes eIF4A binding to specific mRNA sequences with recognition motifs in the 5-UTRs (IC50=2 nM) and interferes with the assembly of the eIF4F initiation complex[1]. Zotatifin shows robust antiviral effects, it effectively reduces viral infectivity by inhibiting SARS-CoV-2 NP protein biogenesis (IC90=37 nM)[2]. Zotatifin induces cell apoptosis[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: eFT226. CAS No. 2098191-53-6. Pack Sizes: 1 mg; 2 mg; 5 mg; 10 mg. Product ID: HY-112163. | |
| Zotepine | Zotepine. Group: Biochemicals. Grades: Highly Purified. CAS No. 26615-21-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Zotepine Impurity1 | Zotepine Impurity1. Uses: For analytical and research use. CAS No. 63720-83-2. Molecular formula: C18H18ClNO2S. Mole weight: 347.86. Catalog: APB63720832. | |
| Zotepine impurity 10 | Zotepine impurity 10. Uses: For analytical and research use. CAS No. 19905-07-8. Molecular formula: C14H9ClS. Mole weight: 244.74. Catalog: APB19905078. | |
| Zotepine impurity 11 | Zotepine impurity 11. Uses: For analytical and research use. CAS No. 4789-54-2. Molecular formula: C22H24ClNO5S. Mole weight: 449.95. Catalog: APB4789542. | |
| Zotepine Impurity2 | Zotepine Impurity2. Uses: For analytical and research use. CAS No. 78105-23-4. Molecular formula: C18H18ClNO2S. Mole weight: 347.86. Catalog: APB78105234. | |
| Zotepine impurity 3 | Zotepine impurity 3. Uses: For analytical and research use. CAS No. 1514918-29-6. Molecular formula: C18H18ClNO3S. Mole weight: 363.86. Catalog: APB1514918296. | |
| Zotepine impurity 4 | Zotepine impurity 4. Uses: For analytical and research use. CAS No. 47289-31-6. Molecular formula: C19H20ClNOS. Mole weight: 345.89. Catalog: APB47289316. | |
| Zotepine impurity 5 | Zotepine impurity 5. Uses: For analytical and research use. CAS No. 93665-48-6. Molecular formula: C21H25ClN2OS. Mole weight: 388.95. Catalog: APB93665486. | |
| Zotepine impurity 6 | Zotepine impurity 6. Uses: For analytical and research use. CAS No. 6823-52-5. Molecular formula: C22H24ClNO5S. Mole weight: 449.95. Catalog: APB6823525. | |
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