Belgium · Impurity Reference Standards

Impurity Standards supply to Belgium

Zemixal supplies 20,060 products from its impurity reference standards range to buyers in Belgium. Locally, the main users are in petrochemicals & polymers, vaccines & biologics and generic & innovative pharma. Regular consignments go to industrial centres such as Antwerp port cluster, Ghent and Walloon Brabant (Wavre). Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Belgium Sample products

20,060products in this division

21–27 dsea transit from India

3–5 dair freight

6categories

Supplying impurity reference standards to Belgium

By sea, containers and LCL lots take roughly 21–27 days to Antwerp and Zeebrugge. Air cargo to Brussels (BRU) takes 3–5 days, which suits small and urgent packs. The relevant authority is FAMHP / EMA. Our export desk lines up the COA, GHS SDS and shipping documents to match. 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 Belgium

Authority	FAMHP / EMA
Seaports	Antwerp, Zeebrugge, Ghent
Airports	Brussels (BRU), Liège (LGG)
Dangerous goods	IMDG by sea, IATA DGR by air

Belgium 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. The SDS and labels need to be in Dutch, French or German depending on where the product is placed. Medicinal active substances from India require GMP compliance and an EU written confirmation, with FAMHP supervising authorised importers. Hazardous cargo is packed and declared under 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.
21–27 daysOcean transit to Antwerp
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: 28–44 days

By air: about 7–15 days in total.

Documents for Belgium

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 Belgium

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

Full impurity reference standards range

2-Butynoic acid

CAS: 590-93-2
Formula: C₄H₄O₂
MW: 84.07 g/mol

ZX-030557

Methyl 4-amino-2-methoxybenzenecarboxylate

CAS: 27492-84-8
Formula: C₉H₁₁NO₃
MW: 181.19 g/mol

ZX-030558

Metoclopramide Hydrochloride

CAS: 7232-21-5
Formula: C₁₄H₂₅Cl₂N₃O₃
MW: 354.3 g/mol

ZX-030559

Metoclopramide-d3

CAS: 1216522-89-2
Formula: C₁₄H₂₂ClN₃O₂
MW: 302.81 g/mol

ZX-030560

Metomidate Hydrochloride

CAS: 35944-74-2
Formula: C₁₃H₁₅ClN₂O₂
MW: 266.72 g/mol

ZX-030561

Metopimazine

CAS: 14008-44-7
Formula: C₂₂H₂₇N₃O₃S₂
MW: 445.6 g/mol

ZX-030562

Metopimazine Acid

CAS: 18182-00-8
Formula: C₂₂H₂₆N₂O₄S₂
MW: 446.6 g/mol

ZX-030563

2-(Methylsulfonyl) Phenothiazine

CAS: 23503-68-6
Formula: C₁₃H₁₁NO₂S₂
MW: 277.4 g/mol

ZX-030564

Metoprolol EP Impurity M dihydrochloride

CAS: 73313-36-7
Formula: C₉H₂₄Cl₂N₂O
MW: 247.2 g/mol

ZX-030565

Metoprolol EP Impurity M

CAS: 343785-33-1
Formula: C₉H₂₂N₂O
MW: 174.28 g/mol

ZX-030566

(S)-Metoprolol

CAS: 81024-42-2
Formula: C₁₅H₂₅NO₃
MW: 267.36 g/mol

ZX-030567

2-(Phenoxymethyl)oxirane

CAS: 122-60-1
Formula: C₉H₁₀O₂
MW: 150.17 g/mol

ZX-030568

Questions

Impurity Reference Standards for Belgium

Do you ship impurity standards to Belgium?

Yes. We ship by sea to Antwerp and Zeebrugge, 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 Belgium?

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 FAMHP / EMA is agreed with you at quote stage.

How long does delivery to Belgium take?

Allow 21–27 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 Belgium

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

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