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Canada · Impurity Reference Standards

Impurity Reference Standards for Canada

Buyers in Canada can order any of the 20,060 products in our impurity reference standards division. In Canada the strongest demand is from generic & biotech pharmaceuticals, petrochemicals & oil sands and mining & metals. Typical delivery points include Greater Toronto Area, Montreal and Vancouver. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Canada Sample products
20,060products in this division
30–42 dsea transit from India
4–6 dair freight
6categories

Supplying impurity reference standards to Canada

Sea freight reaches Vancouver and Montreal in about 30–42 days port to port. Urgent or small lots fly to Toronto Pearson (YYZ) in 4–6 days. Import compliance for this category sits with Health Canada (Health Products and Food Branch), 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 Canada

AuthorityHealth Canada (Health Products and Food Branch)
SeaportsVancouver, Montreal, Halifax
AirportsToronto Pearson (YYZ), Montreal (YUL)
Dangerous goodsIMDG by sea, IATA DGR by air

Under CEPA 1999, imported substances must be on the Domestic Substances List or notified to Environment and Climate Change Canada and Health Canada under the New Substances Notification Regulations. Hazardous products supplied to workplaces need WHMIS 2015 SDS and labels in English and French. APIs require a Drug Establishment Licence held by the Canadian importer and GMP evidence for the foreign site. Precursors fall under the Precursor Control Regulations, and customs data can be supplied on a Canada Customs Invoice or commercial invoice.

From order to delivery

  1. 1–2 daysQuote and document set agreed

    Price, pack sizes, Incoterm and the paperwork list are confirmed in writing.

  2. 3–7 daysPacking for export

    Stock items are packed in UN-rated drums or cartons. Made-to-order material adds its own lead time.

  3. 1–3 daysExport clearance at Nhava Sheva or Mundra

    Shipping bill filed, dangerous goods declared under IMDG where needed.

  4. 30–42 daysOcean transit to Vancouver

    Port-to-port time depends on the vessel schedule and any transhipment.

  5. 2–5 daysImport clearance

    Your broker clears the goods against local rules. Chemical oversight: ECCC & Health Canada (CEPA 1999, DSL/NDSL).

Indicative total by sea: 37–59 days

By air: about 8–16 days in total.

Documents for Canada

  • Commercial Invoice
  • Packing List
  • Bill of Lading / Air Waybill
  • Certificate of Origin
  • Certificate of Analysis (COA)
  • Safety Data Sheet (16-section GHS)
  • DSL status or New Substances Notification confirmation (by importer)
  • WHMIS 2015-compliant bilingual SDS and labels (English/French)
  • Canada Customs Invoice or commercial invoice with CBSA data
  • Precursor import permit where applicable
  • Dangerous Goods Declaration (IMDG/IATA) where applicable

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 Canada

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

Full impurity reference standards range
Questions

Impurity Reference Standards for Canada

Can Zemixal deliver impurity reference standards to Canada?
Yes. We ship by sea to Vancouver and Montreal, 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 Canada?
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 Health Canada (Health Products and Food Branch) is agreed with you at quote stage.
How long does delivery to Canada take?
Allow 30–42 days for ocean transit or 4–6 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 Canada

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

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