Poland · Pharmaceutical Intermediates

Pharmaceutical Intermediates shipped to Poland

Buyers in Poland can order any of the 14,468 products in our pharmaceutical intermediates division. In Poland the strongest demand is from generic pharmaceuticals, nitrogen fertilisers & caprolactam and petroleum refining & petrochemicals. Typical delivery points include Warsaw, Płock and Tarnów. Typical customers for this division are API manufacturers, CDMOs and CMOs and medicinal and discovery chemistry groups.

Poland Sample products

14,468products in this division

28–36 dsea transit from India

3–5 dair freight

4categories

Supplying pharmaceutical intermediates to Poland

Sea freight reaches Gdańsk and Gdynia in about 28–36 days port to port. Urgent or small lots fly to Warsaw Chopin (WAW) in 3–5 days. Import compliance for this category sits with URPL (Office for Registration of Medicinal Products) / GIF / 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 Poland

Authority	URPL (Office for Registration of Medicinal Products) / GIF / EMA
Seaports	Gdańsk, Gdynia, Szczecin–Świnoujście
Airports	Warsaw Chopin (WAW), Katowice (KTW)
Dangerous goods	IMDG by sea, IATA DGR by air

Poland applies EU REACH and CLP. The importer or an Only Representative registers substances imported at 1 tonne or more per year and must supply SDS and labels in Polish. API imports need an EU written confirmation or equivalent GMP standing, and importing sites are supervised by the Chief Pharmaceutical Inspectorate (GIF), with URPL handling medicinal product registration. Customs clearance requires the importer's EORI number, and dangerous goods are declared under IMDG or IATA rules.

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 Gdańsk
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 7–15 days in total.

Documents for Poland

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

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 Poland

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

Full pharmaceutical intermediates range

N-Methyl-1-(phenylmethyl)-3-(1,2,3,6-tetrahydro-1-methyl-4-pyridinyl)-1H-indole-5-ethanesulfonamide

CAS: 894351-86-1
Formula: C₂₄H₂₉N₃O₂S
MW: 423.6 g/mol

ZX-044009

2,3,6-Triaminopyridine Dihydrochloride

CAS: 20284-90-6
Formula: C₅H₁₀Cl₂N₄
MW: 197.06 g/mol

ZX-044011

N-[6-(Trifluoromethoxy)-2-benzothiazolyl]urea

CAS: 1456696-94-8
Formula: C₉H₆F₃N₃O₂S
MW: 277.23 g/mol

ZX-044012

Methyl L-Tyrosinate

CAS: 1080-06-4
Formula: C₁₀H₁₃NO₃
MW: 195.21 g/mol

ZX-044013

R-Venlafaxine Di-p-toluoyl-D-tartrate Salt

CAS: 272788-00-8
Formula: C₃₇H₄₅NO₁₀
MW: 663.8 g/mol

ZX-044014

S-Venlafaxine-di-p-toluoyl-L-tartrate Salt (2:1)

CAS: 93471-25-1
Formula: C₅₄H₇₂N₂O₁₂
MW: 941.2 g/mol

ZX-044015

L-Valine tert-Butyl Ester Hydrochloride

CAS: 13518-40-6
Formula: C₉H₂₀ClNO₂
MW: 209.71 g/mol

ZX-044016

D-Valine Benzyl Ester p-Toluenesulfonate

CAS: 17662-84-9
Formula: C₁₉H₂₅NO₅S
MW: 379.5 g/mol

ZX-044017

3-Methyl-7-propylxanthine

CAS: 55242-64-3
Formula: C₉H₁₂N₄O₂
MW: 208.22 g/mol

ZX-044019

Resorufin Sodium Salt ~90%

CAS: 34994-50-8
Formula: C₁₂H₆NNaO₃
MW: 235.17 g/mol

ZX-044027

4-Bromo-3-oxo-butyric acid ethyl ester

CAS: 13176-46-0
Formula: C₆H₉BrO₃
MW: 209.04 g/mol

ZX-044037

2-Cyano Loratadine

CAS: 860010-31-7
Formula: C₂₃H₂₂ClN₃O₂
MW: 407.9 g/mol

ZX-044038

Questions

Pharmaceutical Intermediates for Poland

Can Zemixal deliver pharmaceutical intermediates to Poland?

Yes. We ship by sea to Gdańsk and Gdynia, 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 Poland?

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 URPL (Office for Registration of Medicinal Products) / GIF / EMA is agreed with you at quote stage.

How long does delivery to Poland take?

Allow 28–36 days for ocean transit or 3–5 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 Poland

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

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