Croatia · Impurity Reference Standards

Impurity Reference Standards for Croatia

The impurity reference standards division counts 20,060 products, and each one can be quoted for delivery to Croatia. In Croatia the strongest demand is from generic & branded pharmaceuticals, fertilisers and petroleum refining. Regular consignments go to industrial centres such as Zagreb, Kutina and Rijeka. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Croatia Sample products

20,060products in this division

20–28 dsea transit from India

4–6 dair freight

6categories

Supplying impurity reference standards to Croatia

By sea, containers and LCL lots take roughly 20–28 days to Rijeka and Ploče. Air cargo to Zagreb (ZAG) takes 4–6 days, which suits small and urgent packs. The relevant authority is HALMED / EMA. Our export desk lines up the COA, GHS SDS and shipping documents to match. 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 Croatia

Authority	HALMED / EMA
Seaports	Rijeka, Ploče, Split
Airports	Zagreb (ZAG), Split (SPU)
Dangerous goods	IMDG by sea, IATA DGR by air

Croatia follows EU REACH and CLP. For substances at 1 tonne or more per year, registration rests with the EU importer or an Only Representative, and SDS and labels must be in Croatian. API imports require an EU written confirmation or equivalent GMP standing, and the importer must hold a manufacturing or import authorisation from HALMED. Clearance at Rijeka or Ploče uses the standard EU single administrative document with the importer's EORI number, and 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.
20–28 daysOcean transit to Rijeka
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: 27–45 days

By air: about 8–16 days in total.

Documents for Croatia

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 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 Croatia

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

Full impurity reference standards range

Fluphenazine Decanoate N-Oxide

CAS: 76005-64-6
Formula: C₃₂H₄₄F₃N₃O₃S
MW: 607.8 g/mol

ZX-029577

Fluphenazine Decanoate EP Impurity F

CAS: 13220-06-9
Formula: C₃₃H₄₆F₃N₃O₂S
MW: 605.8 g/mol

ZX-029578

7-Hydroxy Fluphenazine

CAS: 33098-48-5
Formula: C₂₂H₂₆F₃N₃O₂S
MW: 453.5 g/mol

ZX-029579

10-(3-Bromopropyl)-2-(trifluoromethyl)-10H-phenothiazine

CAS: 1675-43-0
Formula: C₁₆H₁₃BrF₃NS
MW: 388.2 g/mol

ZX-029580

Fluphenazine Decanoate Di-N-Oxide

CAS: 76005-65-7
Formula: C₃₂H₄₄F₃N₃O₄S
MW: 623.8 g/mol

ZX-029581

Fluphenazine Decanoate s-Oxide

CAS: 64610-50-0
Formula: C₃₂H₄₄F₃N₃O₃S
MW: 607.8 g/mol

ZX-029582

2-(4-(3-(2-(Trifluoromethyl)-10H-phenothiazin-10-yl)propyl)piperazin-1-yl)ethyl stearate

CAS: 2285-19-0
Formula: C₄₀H₆₀F₃N₃O₂S
MW: 704 g/mol

ZX-029583

2-Amino-3-nitro-6-chloropyridine

CAS: 27048-04-0
Formula: C₅H₄ClN₃O₂
MW: 173.56 g/mol

ZX-029584

2-Amino-3-nitro-6-(4'-fluorobenzylamino)-pyridine

CAS: 33400-49-6
Formula: C₁₂H₁₁FN₄O₂
MW: 262.24 g/mol

ZX-029585

Flurbiprofen Glyceryl Ester

CAS: 124635-84-3
Formula: C₁₈H₁₉FO₄
MW: 318.3 g/mol

ZX-029586

4'-Hydroxy Flurbiprofen

CAS: 52807-12-2
Formula: C₁₅H₁₃FO₃
MW: 260.26 g/mol

ZX-029587

(2-Fluoro-4-biphenyl)acetic Acid

CAS: 5001-96-7
Formula: C₁₄H₁₁FO₂
MW: 230.23 g/mol

ZX-029588

Questions

Impurity Reference Standards for Croatia

Do you ship impurity standards to Croatia?

Yes. We ship by sea to Rijeka and Ploče, 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 Croatia?

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 HALMED / EMA is agreed with you at quote stage.

How long does delivery to Croatia take?

Allow 20–28 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 Croatia

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

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