Finland · Impurity Reference Standards

Impurity Standards supply to Finland

The impurity reference standards division counts 20,060 products, and each one can be quoted for delivery to Finland. Locally, the main users are in pulp & paper chemicals, refining & renewable fuels and inorganic chemicals & battery materials. Typical delivery points include Porvoo (Kilpilahti), Kokkola and Turku. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Finland Sample products

20,060products in this division

28–38 dsea transit from India

3–5 dair freight

6categories

Supplying impurity reference standards to Finland

Sea freight reaches HaminaKotka and Helsinki (Vuosaari) in about 28–38 days port to port. Urgent or small lots fly to Helsinki (HEL) in 3–5 days. Import compliance for this category sits with Fimea / 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 Finland

Authority	Fimea / EMA
Seaports	HaminaKotka, Helsinki (Vuosaari), Rauma
Airports	Helsinki (HEL)
Dangerous goods	IMDG by sea, IATA DGR by air

Finland applies EU REACH and CLP. When a substance enters the EU at 1 tonne or more per year, the EU importer or an Only Representative for the Indian manufacturer must hold the registration. SDS and labels are expected in Finnish and Swedish. Active substances for medicinal use need GMP compliance and an EU written confirmation, and Fimea supervises authorised importers. Hazardous materials must be packed and declared to IMDG or IATA DGR, and customs entry needs the importer's EORI number.

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.
28–38 daysOcean transit to HaminaKotka
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: 35–55 days

By air: about 7–15 days in total.

Documents for Finland

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 OR declaration (substances ≥1 t/yr)
EU Written Confirmation for API imports (Art. 46b Directive 2001/83/EC)
Dangerous Goods Declaration (IMDG/IATA) where applicable
Importer's EORI number

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 Finland

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

Full impurity reference standards range

Paliperidone palmitate

CAS: 199739-10-1
Formula: C₃₉H₅₇FN₄O₄
MW: 664.9 g/mol

ZX-026282

5-Fluoro Paliperidone

CAS: 1346598-34-2
Formula: C₂₃H₂₇FN₄O₃
MW: 426.5 g/mol

ZX-026283

Paliperidone N-Oxide

CAS: 761460-08-6
Formula: C₂₃H₂₇FN₄O₄
MW: 442.5 g/mol

ZX-026284

3-Ethyl-9-hydroxy-2-methyl-6,7,8,9-tetrahydro-pyrido[1,2-a]pyrimidin-4-one

CAS: 849903-79-3
Formula: C₁₁H₁₆N₂O₂
MW: 208.26 g/mol

ZX-026285

Paliperidone Palmitate N-Oxide

CAS: 1404053-60-6
Formula: C₃₉H₅₇FN₄O₅
MW: 680.9 g/mol

ZX-026286

3-(2-Chloroethyl)-7,8-dihydro-2-methyl-4H-pyrido[1,2-a]pyrimidine-4,9(6H)-dione

CAS: 1138463-56-5
Formula: C₁₁H₁₃ClN₂O₂
MW: 240.68 g/mol

ZX-026287

3-(2-Chloroethyl)-9-hydroxy-2-methylpyrido[1,2-a]pyrimidin-4-one

CAS: 260273-82-3
Formula: C₁₁H₁₁ClN₂O₂
MW: 238.67 g/mol

ZX-026288

Defluoro Paliperidone

CAS: 1380413-60-4
Formula: C₂₃H₂₈N₄O₃
MW: 408.5 g/mol

ZX-026289

Paliperidone Z-Oxime

CAS: 1388021-47-3
Formula: C₂₃H₂₈F₂N₄O₃
MW: 446.5 g/mol

ZX-026290

Tetradecanoic Acid 3-[2-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-6,7,8,9-tetrahydro-2-methyl-4-oxo-4H-pyrido[1,2a]pyrimidin-9-yl ester

CAS: 1172995-11-7
Formula: C₃₇H₅₃FN₄O₄
MW: 636.8 g/mol

ZX-026291

(S,S)-Palonosetron Acid

CAS: 2407763-21-5
Formula: C₁₉H₂₆N₂O₂
MW: 314.4 g/mol

ZX-026292

Disodium Pamidrote

CAS: 109552-15-0
Formula: C₃H₁₉NNa₂O₁₂P₂
MW: 369.11 g/mol

ZX-026293

Questions

Impurity Reference Standards for Finland

Can Zemixal deliver impurity reference standards to Finland?

Yes. We ship by sea to HaminaKotka and Helsinki (Vuosaari), 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 Finland?

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 Fimea / EMA is agreed with you at quote stage.

How long does delivery to Finland take?

Allow 28–38 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.

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 Finland

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

Impurity Reference Standards in nearby countries