Iceland · Pharmaceutical Intermediates

Pharma Intermediates supply to Iceland

The pharmaceutical intermediates division counts 14,468 products, and each one can be quoted for delivery to Iceland. Locally, the main users are in aluminium smelting, geothermal energy & water treatment and fisheries & aquaculture. Typical delivery points include Reykjavík, Hafnarfjörður (Straumsvík) and Grundartangi. Typical customers for this division are API manufacturers, CDMOs and CMOs and medicinal and discovery chemistry groups.

Iceland Sample products

14,468products in this division

32–45 dsea transit from India

4–7 dair freight

4categories

Supplying pharmaceutical intermediates 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 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 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 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 Iceland

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

Full pharmaceutical intermediates range

2-Palmityl-1,3-diolein

CAS: 1716-07-0
Formula: C₅₅H₁₀₂O₆
MW: 859.4 g/mol

ZX-041099

2-Ethyl-5-oxohexyl phthalate

CAS: 40321-98-0
Formula: C₁₆H₂₀O₅
MW: 292.33 g/mol

ZX-041100

Perfluorohexylsulfonamide

CAS: 41997-13-1
Formula: C₆H₂F₁₃NO₂S
MW: 399.13 g/mol

ZX-041101

Bis(1,3-dichloro-2-propyl) phosphate

CAS: 72236-72-7
Formula: C₆H₁₁Cl₄O₄P
MW: 319.9 g/mol

ZX-041102

Perfluorodecanesulfonic acid

CAS: 335-77-3
Formula: C₁₀HF₂₁O₃S
MW: 600.15 g/mol

ZX-041103

Avoralstat

CAS: 918407-35-9
Formula: C₂₈H₂₇N₅O₅
MW: 513.5 g/mol

ZX-041104

N-(Chlorosulfonyl)-N-methyl-beta-alanine methyl ester

CAS: 1250575-99-5
Formula: C₅H₁₀ClNO₄S
MW: 215.66 g/mol

ZX-041105

Ethyl-4,4,4-Trichloro acetoacetate

CAS: 3702-98-5
Formula: C₆H₇Cl₃O₃
MW: 233.5 g/mol

ZX-041106

Ethyl 2,2,4-trichloro-3-oxo-butanoate

CAS: 85153-67-9
Formula: C₆H₇Cl₃O₃
MW: 233.5 g/mol

ZX-041107

Ethyl 4-chloro-3,3-diethoxybutyrate

CAS: 65840-81-5
Formula: C₁₀H₁₉ClO₄
MW: 238.71 g/mol

ZX-041108

Ethyl Stearate

CAS: 111-61-5
Formula: C₂₀H₄₀O₂
MW: 312.5 g/mol

ZX-041109

Ethyl Linoleate

CAS: 544-35-4
Formula: C₂₀H₃₆O₂
MW: 308.5 g/mol

ZX-041110

Questions

Pharmaceutical Intermediates for Iceland

Can Zemixal deliver pharmaceutical intermediates 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 pharma intermediates 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.

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 Iceland

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

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