Type of
Type of
C17H27ClN2O.ClH
Neat
347.32
+5°C
Room Temperature
3-[4-(3-Chlorophenyl)piperazin-1-yl]propyl Isobutyl Ether Hydrochloride, Trazodone Hydrochloride Imp. G (BP) as Hydrochloride, Trazodone Hydrochloride Impurity G and Trazodone Impurity G
Cl.CC(C)COCCCN1CCN(CC1)c2cccc(Cl)c2
1-(3-chlorophenyl)-4-[3-(2-methylpropoxy)propyl]piperazine;hydrochloride
|
Pack Size
SKU
|
Category | Expected Delivery | Price | Quantity | |
|---|---|---|---|---|---|
|
25mg
CE4617.15-25MG
|
|
3-4 weeks |
|
|
|
|
50mg
CE4617.15-50MG
|
|
3-4 weeks |
|
|
|
|
100mg
CE4617.15-100MG
|
|
3-4 weeks |
|
|
|
|
500mg
CE4617.15-500MG
|
|
3-4 weeks |
|
|
|
|
25mg
CD4617.15-25MG
|
|
3-5 weeks |
|
|
|
|
100mg
CD4617.15-4X25MG
|
|
3-5 weeks |
|
|
|
|
25mg
CB4617.15-25MG
|
|
4-5 weeks |
|
|
|
|
100mg
CB4617.15-4X25MG
|
|
4-5 weeks |
|
|
|
|
Request custom package size
|
|
|
|
|
|
Your shopping cart is empty.
select productsSpecifically developed to support early-stage development, drug discovery, R&D, and academia, these standards are ideal for qualitative applications. Every product is tested through a consistent set of analytical techniques to ensure identity and purity, with verified chemical structure and a guaranteed HPLC purity above 95%.
Research Chemicals / Analytical Standards
With Klivon Dynamic range you can count on carefully determined ASSAY values. Best cost-benefit ratio for varied non-compendial applications in compliance with ICH, FDA and WHO guidelines. A final remark (conclusion) bellow of each spectra is added.
Characterized Reference Standards
Our premium range of High Purity Reference Standards designed to meet the most demanding pharmaceutical laboratories and highly critical research, Klivon Beyond is accompanied by a comprehensive certificate of analysis (CoA), also comes with a complete spectrum elucidation report. A final remark (conclusion) or Spectra Interpretation bellow of each spectra is added.
Full Characterized Reference Standards
Our Impurity Characterized Standards portfolio comprises more than 5,000 compounds accompanied by a comprehensive CoA which can be found in 3 product categories that include a set of different analytical techniques for determining Identity and Purity.
We have designed a range of primary API standards manufactured according to international regulations that come with the most extensive Certificate of Analysis which includes Identity checks by several techniques.
Excipients standards comes with a detailed Certificate of Analysis with Identity, Purity and Assay data. They are also suitable for use with non-compendial analytical methods.
We offer tailor-made synthesis services of up to gram-quantities of materials for a wide range of pharmaceutical customers. The customer can order a specific molecule that is only synthesized on your request on the scale, with the purity and with the specification or methods you require.
Read more