Sweden · Impurity Reference Standards

Impurity Reference Standards shipped to Sweden

Zemixal supplies 20,060 products from its impurity reference standards range to buyers in Sweden. In Sweden the strongest demand is from bioprocessing & life-science tools, pharmaceuticals and petrochemicals. Typical delivery points include Stenungsund, Stockholm – Uppsala and Södertälje. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Sweden Sample products

20,060products in this division

26–34 dsea transit from India

3–5 dair freight

6categories

Supplying impurity reference standards 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 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 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 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 Sweden

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

Full impurity reference standards range

Cyanidin Chloride

CAS: 528-58-5
Formula: C₁₅H₁₁ClO₆
MW: 322.69 g/mol

ZX-028752

Cyanocobalamin-b-carboxylic Acid

CAS: 38218-77-8
Formula: C₆₃H₈₇CoN₁₃O₁₅P
MW: 1356.3 g/mol

ZX-028753

Aquocobalamin

CAS: 13422-52-1
Formula: C₆₂H₉₁CoN₁₃O₁₆P
MW: 1364.4 g/mol

ZX-028754

Cyantraniliprole

CAS: 736994-63-1
Formula: C₁₉H₁₄BrClN₆O₂
MW: 473.7 g/mol

ZX-028755

3-Bromo-1-(3-chloropyridin-2-yl)-N-(4-formamido-2-methyl-6-(methylcarbamoyl)phenyl)-1H-pyrazole-5-carboxamide

CAS: 2957882-50-5
Formula: C₁₉H₁₆BrClN₆O₃
MW: 491.7 g/mol

ZX-028756

Dibenzosuberane

CAS: 833-48-7
Formula: C₁₅H₁₄
MW: 194.27 g/mol

ZX-028757

10-Bromo-10,11-dihydro-5H-dibenzo[a,d][7]annulen-5-one

CAS: 24167-44-0
Formula: C₁₅H₁₁BrO
MW: 287.15 g/mol

ZX-028758

Cyclobenzaprine-d3 Hydrochloride

CAS: 1184983-42-3
Formula: C₂₀H₂₂ClN
MW: 314.9 g/mol

ZX-028759

Dodecamethylcyclohexasiloxane

CAS: 540-97-6
Formula: C₁₂H₃₆O₆Si₆
MW: 444.92 g/mol

ZX-028760

Alcophosphamide

CAS: 52336-54-6
Formula: C₇H₁₇Cl₂N₂O₃P
MW: 279.1 g/mol

ZX-028761

(2-Chloroethyl){2-[(3-hydroxypropyl)amino]ethyl}phosphoramidic acid

CAS: 2810251-24-0
Formula: C₇H₁₈ClN₂O₄P
MW: 260.65 g/mol

ZX-028762

N-Dechloroethyl Cyclophosphamide

CAS: 36761-83-8
Formula: C₅H₁₂ClN₂O₂P
MW: 198.59 g/mol

ZX-028763

Questions

Impurity Reference Standards for Sweden

Can Zemixal deliver impurity reference standards 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 impurity standards 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.

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 Sweden

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

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