Czech Republic · Pharmaceutical Intermediates

Pharmaceutical Intermediates for Czech Republic

The pharmaceutical intermediates division counts 14,468 products, and each one can be quoted for delivery to Czech Republic. Demand there comes mainly from generic pharmaceuticals, petrochemicals & refining and automotive components & coatings. Typical delivery points include Prague, Pardubice and Ústí nad Labem. Typical customers for this division are API manufacturers, CDMOs and CMOs and medicinal and discovery chemistry groups.

Czech Republic Sample products

14,468products in this division

28–36 dsea transit from India

4–6 dair freight

4categories

Supplying pharmaceutical intermediates to Czech Republic

Sea freight reaches Hamburg (via rail) and Bremerhaven (via rail) in about 28–36 days port to port. Urgent or small lots fly to Prague (PRG) in 4–6 days. Import compliance for this category sits with SÚKL / EMA, and we prepare the COA, SDS and commercial documents your broker needs. Common grades for this division are Key starting material (KSM) specification, Advanced intermediate (customer spec), Building block, ≥95% / ≥98% purity and Chiral (ee specified).

Grades in this division

Key starting material (KSM) specificationAdvanced intermediate (customer spec)Building block, ≥95% / ≥98% purityChiral (ee specified)Technical gradeLow genotoxic-impurity specification

Pharma compliance in Czech Republic

Authority	SÚKL / EMA
Seaports	Hamburg (via rail), Bremerhaven (via rail), Koper (via rail)
Airports	Prague (PRG), Ostrava (OSR)
Dangerous goods	IMDG by sea, IATA DGR by air

Czech imports fall under EU REACH and CLP. Registration for substances at 1 tonne or more per year is held by the EU importer or an Only Representative, and SDS and labels must be in Czech. APIs need an EU written confirmation or equivalent GMP standing and must go to a SÚKL-authorised importer. Sea cargo can be cleared at Hamburg or Koper, or moved under transit with a T1 document and cleared at a Czech rail terminal, so agree the clearance point before booking.

From order to delivery

1–2 daysQuote and document set agreed
Price, pack sizes, Incoterm and the paperwork list are confirmed in writing.
3–7 daysPacking for export
Stock items are packed in UN-rated drums or cartons. Made-to-order material adds its own lead time.
1–3 daysExport clearance at Nhava Sheva or Mundra
Shipping bill filed, dangerous goods declared under IMDG where needed.
28–36 daysOcean transit to Hamburg (via rail)
Port-to-port time depends on the vessel schedule and any transhipment.
2–5 daysImport clearance
Your broker clears the goods against local rules. Chemical oversight: ECHA (EU REACH & CLP).

Indicative total by sea: 35–53 days

By air: about 8–16 days in total.

Documents for Czech Republic

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
REACH registration number or Only Representative declaration (substances ≥1 t/yr)
SDS in REACH Annex II format in the local language (supplied to the EU importer)
EU Written Confirmation for API imports (Art. 46b Directive 2001/83/EC)
EORI number of the EU importer (customs declaration)
Dangerous Goods Declaration (IMDG/IATA) where applicable
T1 transit document where cleared inland

Categories in pharmaceutical intermediates

Organic Building Blocks 8,529Heterocyclic Building Blocks 2,832Bulk Pharma Intermediates 22 API Process Intermediates & Related Compounds 3,085

A selection we ship to Czech Republic

A rotating sample from the division. Every product in the catalogue can be quoted for this destination.

Full pharmaceutical intermediates range

Foeniculin

CAS: 78259-41-3
Formula: C₁₄H₁₈O
MW: 202.29 g/mol

ZX-034862

Dimethyl2,3-dihydroxysuccinate

CAS: 405897-14-5
Formula: C₆H₁₀O₆
MW: 178.14 g/mol

ZX-034864

2,3-Dihydroxy-4-methoxy-4-oxobutanoic Acid

CAS: 860708-13-0
Formula: C₅H₈O₆
MW: 164.11 g/mol

ZX-034865

1,2,3,4-Tetraphenyl-1,3-cyclopentadiene

CAS: 15570-45-3
Formula: C₂₉H₂₂
MW: 370.5 g/mol

ZX-034867

Tetracontane

CAS: 4181-95-7
Formula: C₄₀H₈₂
MW: 563.1 g/mol

ZX-034868

1-(Cyanomethyl)urea

CAS: 5962-07-2
Formula: C₃H₅N₃O
MW: 99.09 g/mol

ZX-034869

6-Paradol

CAS: 27113-22-0
Formula: C₁₇H₂₆O₃
MW: 278.4 g/mol

ZX-034870

1,2-Dichloropropane

CAS: 78-87-5
Formula: C₃H₆Cl₂
MW: 112.98 g/mol

ZX-034872

Methyl 2,3-dichloropropionate

CAS: 3674-09-7
Formula: C₄H₆Cl₂O₂
MW: 156.99 g/mol

ZX-034874

Propionamide

CAS: 79-05-0
Formula: C₃H₇NO
MW: 73.09 g/mol

ZX-034876

1,2-Dibromobenzene

CAS: 583-53-9
Formula: C₆H₄Br₂
MW: 235.9 g/mol

ZX-034881

2-Cyclohexylidene-acetic Acid Ethyl Ester

CAS: 1552-92-7
Formula: C₁₀H₁₆O₂
MW: 168.23 g/mol

ZX-034882

Questions

Pharmaceutical Intermediates for Czech Republic

Can Zemixal deliver pharmaceutical intermediates to Czech Republic?

Yes. We ship by sea to Hamburg (via rail) and Bremerhaven (via rail), by air cargo or by express courier depending on quantity and urgency. Every lot carries a COA and a 16-section GHS SDS.

Which documents come with a pharma intermediates shipment to Czech Republic?

Commercial invoice, packing list, certificate of analysis and SDS as standard, plus the bill of lading or air waybill and a certificate of origin. Anything specific to SÚKL / EMA is agreed with you at quote stage.

How long does delivery to Czech Republic take?

Allow 28–36 days for ocean transit or 4–6 days by air, plus packing, export clearance and import clearance. The timeline on this page shows each stage.

Can you scale an intermediate from grams to kilograms without changing the route?

For many listed intermediates the gram packs and the kilogram supply come from the same manufacturing route, which keeps the impurity profile consistent. Where scale-up needs a different route, we tell you before you commit and can provide comparison samples so your team can check the new material against the old.

How do you control isomer and enantiomer content?

Positional isomers are controlled by HPLC or GC methods suited to the compound, and chiral intermediates are tested by chiral HPLC to report enantiomeric excess. The limits that apply to your lot appear on the COA. If your process needs tighter limits, state them on the enquiry and we will confirm what can be met.

Other divisions for Czech Republic

Lab Reagents Solvents (HPLC & GC) Biochemicals APIs Impurity Reference Standards Inorganics & Metals Specialty Chemicals

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