Iceland · Impurity Reference Standards

Impurity Reference Standards for Iceland

The impurity reference standards division counts 20,060 products, and each one can be quoted for delivery to Iceland. Demand there comes mainly from aluminium smelting, geothermal energy & water treatment and fisheries & aquaculture. Typical delivery points include Reykjavík, Hafnarfjörður (Straumsvík) and Grundartangi. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Iceland Sample products

20,060products in this division

32–45 dsea transit from India

4–7 dair freight

6categories

Supplying impurity reference standards to Iceland

Sea freight reaches Reykjavík (Sundahöfn) and Hafnarfjörður in about 32–45 days port to port. Urgent or small lots fly to Keflavík (KEF) in 4–7 days. Import compliance for this category sits with Icelandic Medicines Agency / 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 Iceland

Authority	Icelandic Medicines Agency / EMA
Seaports	Reykjavík (Sundahöfn), Hafnarfjörður
Airports	Keflavík (KEF)
Dangerous goods	IMDG by sea, IATA DGR by air

Iceland applies EU REACH and CLP through the EEA Agreement. A substance imported at 1 tonne or more per year must be registered by the importer or by an Only Representative, and SDS and labels are expected in Icelandic. Medicinal active substances follow EEA GMP rules under the Icelandic Medicines Agency. Indian-origin goods that meet the rules can claim India–EFTA TEPA preferences when a valid proof of origin is provided. Dangerous goods must be declared under IMDG or IATA.

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.
32–45 daysOcean transit to Reykjavík (Sundahöfn)
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 (EEA REACH & CLP) / Environment Agency of Iceland.

Indicative total by sea: 39–62 days

By air: about 8–17 days in total.

Documents for Iceland

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, EEA)
Written Confirmation for API imports (EEA application of Directive 2001/83/EC)
Dangerous Goods Declaration (IMDG/IATA) where applicable
Certificate of Origin supporting India–EFTA TEPA preferences

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 Iceland

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

Full impurity reference standards range

3-(2-Thienyl)-L-alanine

CAS: 22951-96-8
Formula: C₇H₉NO₂S
MW: 171.22 g/mol

ZX-031252

Nitrosophenylhydrazin

CAS: 614-01-7
Formula: C₆H₇N₃O
MW: 137.14 g/mol

ZX-031253

Psi-Tropine

CAS: 135-97-7
Formula: C₈H₁₅NO
MW: 141.21 g/mol

ZX-031254

4-Bromo-1-Butene

CAS: 5162-44-7
Formula: C₄H₇Br
MW: 135 g/mol

ZX-031255

Irganox 1035

CAS: 41484-35-9
Formula: C₃₈H₅₈O₆S
MW: 642.9 g/mol

ZX-031256

4-Carboxyphenylboronic acid

CAS: 14047-29-1
Formula: C₇H₇BO₄
MW: 165.94 g/mol

ZX-031257

2-Methyl-4,6-bis(octylsulfanylmethyl)phenol

CAS: 110553-27-0
Formula: C₂₅H₄₄OS₂
MW: 424.8 g/mol

ZX-031258

1-(Isopropylamino)-3-(naphthalen-2-yloxy)propan-2-ol

CAS: 2007-72-9
Formula: C₁₆H₂₁NO₂
MW: 259.34 g/mol

ZX-031260

Diflubenzuron

CAS: 35367-38-5
Formula: C₁₄H₉ClF₂N₂O₂
MW: 310.68 g/mol

ZX-031262

3,5-Dibenzyloxyphenylglyoxal hydrate

CAS: 59229-14-0
Formula: C₂₂H₂₀O₅
MW: 364.4 g/mol

ZX-031263

Flufenacet

CAS: 142459-58-3
Formula: C₁₄H₁₃F₄N₃O₂S
MW: 363.33 g/mol

ZX-031264

2,3-Dichloro-1-propanol

CAS: 616-23-9
Formula: C₃H₆Cl₂O
MW: 128.98 g/mol

ZX-031265

Questions

Impurity Reference Standards for Iceland

Can Zemixal deliver impurity reference standards to Iceland?

Yes. We ship by sea to Reykjavík (Sundahöfn) and Hafnarfjörður, 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 Iceland?

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 Icelandic Medicines Agency / EMA is agreed with you at quote stage.

How long does delivery to Iceland take?

Allow 32–45 days for ocean transit or 4–7 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 Iceland

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

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