Slovakia · Impurity Reference Standards

Impurity Reference Standards for Slovakia

The impurity reference standards division counts 20,060 products, and each one can be quoted for delivery to Slovakia. Demand there comes mainly from automotive manufacturing, petroleum refining and fertilisers & rubber chemicals. Typical delivery points include Bratislava, Šaľa and Hlohovec. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Slovakia Sample products

20,060products in this division

28–36 dsea transit from India

4–6 dair freight

6categories

Supplying impurity reference standards to Slovakia

Sea freight reaches Hamburg (via rail) and Koper (via rail) in about 28–36 days port to port. Urgent or small lots fly to Bratislava (BTS) in 4–6 days. Import compliance for this category sits with ŠÚKL (State Institute for Drug Control) / EMA, and we prepare the COA, SDS and commercial documents your broker needs. Common grades for this division are Impurity reference standard with characterisation data, Secondary / working standard, Stable-isotope labelled standard and Nitrosamine (NDSRI) standard.

Grades in this division

Impurity reference standard with characterisation dataSecondary / working standardStable-isotope labelled standardNitrosamine (NDSRI) standardMetabolite standardCustom synthesised impurity

Pharma compliance in Slovakia

Authority	ŠÚKL (State Institute for Drug Control) / EMA
Seaports	Hamburg (via rail), Koper (via rail), Constanța (via Danube barge)
Airports	Bratislava (BTS), Košice (KSC)
Dangerous goods	IMDG by sea, IATA DGR by air

Slovakia follows EU REACH and CLP. The importer or an Only Representative registers substances imported at 1 tonne or more per year and provides SDS and labels in Slovak. APIs need an EU written confirmation or equivalent GMP standing and an importer authorised by ŠÚKL. Sea cargo arrives via Hamburg or Koper and moves inland by rail, sometimes under a T1 transit document, and much air cargo lands in Vienna before trucking to Bratislava. Dangerous goods follow 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 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 Slovakia

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 impurity reference standards

API Impurities 9,055Pharmacopeial Impurities (EP / USP / BP) 3,890Nitrosamine Impurities 382Stable Isotope Labelled Standards (Deuterated, 13C, 15N) 976Metabolites & Degradation Products 2,569API Reference Standards 3,188

A selection we ship to Slovakia

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

Full impurity reference standards range

Lidocaine EP Impurity H

CAS: 1131-01-7
Formula: C₁₀H₁₂ClNO
MW: 197.66 g/mol

ZX-005800

Linezolid USP Related Compound C

CAS: 168828-90-8
Formula: C₁₄H₁₈FN₃O₃
MW: 295.31 g/mol

ZX-005801

Linezolid USP Related Compound D

CAS: 174649-09-3
Formula: C₁₅H₁₉FN₂O₆S
MW: 374.4 g/mol

ZX-005802

Liothyronine EP Impurity B (Dihydrate Salt)

CAS: 18835-59-1
Formula: C₉H₁₃I₂NO₅
MW: 469.01 g/mol

ZX-005803

Liothyronine EP Impurity B (Freebase)

CAS: 300-39-0
Formula: C₉H₉I₂NO₃
MW: 432.98 g/mol

ZX-005804

Lisinopril EP Impurity B (Freebase)

CAS: 104-15-4
Formula: C₇H₈O₃S
MW: 172.2 g/mol

ZX-005805

Lisinopril EP Impurity B (Monohydrate Salt)

CAS: 6192-52-5
Formula: C₇H₁₀O₄S
MW: 190.22 g/mol

ZX-005806

Lomustine EP Impurity C

CAS: 2387-23-7
Formula: C₁₃H₂₄N₂O
MW: 224.34 g/mol

ZX-005807

Loperamide EP Impurity G

CAS: 109572-89-6
Formula: C₂₉H₃₃ClN₂O₃
MW: 493 g/mol

ZX-005808

Loratadine EP Impurity G

CAS: 38092-89-6
Formula: C₂₀H₂₁ClN₂
MW: 324.8 g/mol

ZX-005809

Lurasidone EP Impurity B

CAS: 186204-36-4
Formula: C₁₉H₂₆N₃S⁺
MW: 328.5 g/mol

ZX-005810

Lurasidone EP Impurity B (Methanesulfonate salt)

CAS: 186204-37-5
Formula: C₂₀H₂₉N₃O₃S₂
MW: 423.6 g/mol

ZX-005811

Questions

Impurity Reference Standards for Slovakia

Can Zemixal deliver impurity reference standards to Slovakia?

Yes. We ship by sea to Hamburg (via rail) and Koper (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 impurity standards shipment to Slovakia?

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 ŠÚKL (State Institute for Drug Control) / EMA is agreed with you at quote stage.

How long does delivery to Slovakia 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.

How is the purity of an impurity standard determined?

Purity is usually assigned by HPLC area percentage, supported by structural confirmation from NMR and mass spectrometry. Where needed, water content, residual solvents or a mass balance approach are added. The methods used and the results for your lot are listed on the certificate of analysis that comes with the vial.

Can I use your impurity standards in place of official pharmacopoeial references?

Our standards are secondary or research materials, not official pharmacopoeial references. Many laboratories use them for method development, peak identification and routine testing, and keep official references for disputes or regulatory submissions where these are mandated. Your quality system and regulator decide which reference is acceptable for each test.

Other divisions for Slovakia

Lab Reagents Solvents (HPLC & GC) Biochemicals APIs Pharmaceutical Intermediates Inorganics & Metals Specialty Chemicals

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