Sweden · Pharmaceutical Intermediates

Pharmaceutical Intermediates for Sweden

The pharmaceutical intermediates division counts 14,468 products, and each one can be quoted for delivery to Sweden. Locally, the main users are in bioprocessing & life-science tools, pharmaceuticals and petrochemicals. Typical delivery points include Stenungsund, Stockholm – Uppsala and Södertälje. Typical customers for this division are API manufacturers, CDMOs and CMOs and medicinal and discovery chemistry groups.

Sweden Sample products

14,468products in this division

26–34 dsea transit from India

3–5 dair freight

4categories

Supplying pharmaceutical intermediates to Sweden

Sea freight reaches Gothenburg and Stockholm (Norvik) in about 26–34 days port to port. Urgent or small lots fly to Stockholm Arlanda (ARN) in 3–5 days. Import compliance for this category sits with Swedish Medical Products 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 Sweden

Authority	Swedish Medical Products Agency / EMA
Seaports	Gothenburg, Stockholm (Norvik), Helsingborg
Airports	Stockholm Arlanda (ARN), Gothenburg Landvetter (GOT)
Dangerous goods	IMDG by sea, IATA DGR by air

Sweden applies EU REACH and CLP. Substances imported at 1 tonne or more per year must be registered by the EU importer or by an Only Representative for the Indian manufacturer, and labels and SDS must be in Swedish. Many chemical products must also be notified to the KemI products register by the Swedish importer. Medicinal active substances need GMP compliance and an EU written confirmation, with the Swedish Medical Products Agency supervising importers. Dangerous goods follow IMDG or IATA DGR, and customs 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.
26–34 daysOcean transit to Gothenburg
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: 33–51 days

By air: about 7–15 days in total.

Documents for Sweden

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 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 Sweden

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

Full pharmaceutical intermediates range

FMOC-2-Aminobutric Acid

CAS: 135112-27-5
Formula: C₁₉H₁₉NO₄
MW: 325.4 g/mol

ZX-019377

FMOC-D-Citrulline

CAS: 200344-33-8
Formula: C₂₁H₂₃N₃O₅
MW: 397.4 g/mol

ZX-019378

FMOC-D-Norleucine

CAS: 112883-41-7
Formula: C₂₁H₂₃NO₄
MW: 353.4 g/mol

ZX-019379

Terephthalic -d4-Acid, for spectroscopy, for NMR

CAS: 60088-54-2
Formula: C₈H₆O₄
MW: 170.15 g/mol

ZX-019381

Sodium Diacetate, pure

CAS: 126-96-5
Formula: C₄H₇NaO₄
MW: 142.09 g/mol

ZX-019409

Sodium Dihydrogen Citrate, ACS, AR

CAS: 18996-35-5
Formula: C₆H₇NaO₇
MW: 214.1 g/mol

ZX-019410

Benzoic-d5 Acid, for spectroscopy, for NMR

CAS: 1079-02-3
Formula: C₇H₆O₂
MW: 127.15 g/mol

ZX-019417

Biphenyl-d10, for spectroscopy, for NMR

CAS: 1486-01-7
Formula: C₁₂H₁₀
MW: 164.27 g/mol

ZX-019418

Quinine Glycero Phosphate, AR

CAS: 146-39-4
Formula: C₄₃H₅₇N₄O₁₀P
MW: 820.9 g/mol

ZX-019425

Quinine Sulphate, AR

CAS: 6119-70-6
Formula: C₄₀H₅₄N₄O₁₀S
MW: 782.9 g/mol

ZX-019426

Ammonium-d4 Formate-d, for spectroscopy, for NMR

CAS: 65387-23-7
Formula: CH₅NO₂
MW: 68.09 g/mol

ZX-019432

N N N -Tetrakis (4-Aminophenyl)-1 4-phenylenediamine

CAS: 3283-07-6
Formula: C₃₀H₂₈N₆
MW: 472.6 g/mol

ZX-019452

Questions

Pharmaceutical Intermediates for Sweden

Can Zemixal deliver pharmaceutical intermediates to Sweden?

Yes. We ship by sea to Gothenburg and Stockholm (Norvik), 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 Sweden?

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 Swedish Medical Products Agency / EMA is agreed with you at quote stage.

How long does delivery to Sweden take?

Allow 26–34 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.

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 Sweden

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

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