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Chemicals for pharmaceutical manufacturing and QC

Building blocks, intermediates, APIs, impurity standards and chromatography solvents for drug developers, formulators and release laboratories.

Products used in pharmaceutical manufacturing and QC

35,713–35,736 of 35,907 products
Xylopentaose
CAS
49694-20-4
Formula
C25H42O21
MW
678.6 g/mol
ZX-042690
Xylotetrose
CAS
22416-58-6
Formula
C20H34O17
MW
546.5 g/mol
ZX-042689
Xylotriose
CAS
47592-59-6
Formula
C15H26O13
MW
414.36 g/mol
ZX-042688
Z-Butene
CAS
590-18-1
Formula
C4H8
MW
56.11 g/mol
ZX-045904
Z-DL-Val-OH
CAS
3588-63-4
Formula
C13H17NO4
MW
251.28 g/mol
ZX-035549
Z-Gly-Pro-OH
CAS
1160-54-9
Formula
C15H18N2O5
MW
306.31 g/mol
ZX-040521
Z-L-Norvaline
CAS
21691-44-1
Formula
C13H17NO4
MW
251.28 g/mol
ZX-043902
Z-Orn(Boc)-OH
CAS
7733-29-1
Formula
C18H26N2O6
MW
366.4 g/mol
ZX-035158
Questions

Buying for pharmaceutical manufacturing and QC

Can I buy an API and its pharmacopoeial impurities in one enquiry?
Yes. Add the API and the named impurities to the quote panel together. We confirm which impurity standards are available from stock, which need synthesis and what characterisation data comes with each, so your method validation and supply qualification can run in parallel.
Are excipients available alongside the active ingredient?
Common excipients such as microcrystalline cellulose, lactose monohydrate, povidone and magnesium stearate can be quoted with pharmacopoeial documentation where the producer supplies it. State the monograph and edition you work to, and the COA will report against it.
How do you handle solvents that are controlled precursors?
Some solvents and reagents used in drug synthesis are listed precursors in India or at destination. We flag these on the quotation and may ask for an end-use declaration or import permit before dispatch. Sharing your licence details early avoids delays.

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