(1R,3S,5R)-2-(tert-Butoxycarbonyl)-2-azabicyclo[3.1.0]hexane-3-carboxylic acid
- CAS
- 197142-34-0
- Formula
- C11H17NO4
- MW
- 227.26 g/mol
ZX-045082
Denmark · Impurity Reference Standards
Denmark Sample products
Impurity Standards supply to Denmark
Buyers in Denmark can order any of the 20,060 products in our impurity reference standards division. Locally, the main users are in insulin & diabetes care, industrial enzymes & fermentation and biotech & life-science research. Typical delivery points include Greater Copenhagen / Medicon Valley, Kalundborg and Aarhus. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.
Denmark Sample products20,060products in this division
26–34 dsea transit from India
3–5 dair freight
6categories
Supplying impurity reference standards to Denmark
Sea freight reaches Aarhus and Copenhagen in about 26–34 days port to port. Urgent or small lots fly to Copenhagen (CPH) in 3–5 days. Import compliance for this category sits with Danish Medicines 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 Denmark
| Authority | Danish Medicines Agency / EMA |
|---|---|
| Seaports | Aarhus, Copenhagen, Fredericia |
| Airports | Copenhagen (CPH), Billund (BLL) |
| Dangerous goods | IMDG by sea, IATA DGR by air |
Danish imports fall under EU REACH and CLP. At 1 tonne or more per year, a substance must be registered by the EU importer or by an Only Representative appointed by the Indian maker. Labels and SDS must be in Danish. Active substances for medicines need GMP compliance and an EU written confirmation, and the Danish Medicines Agency supervises authorised importers. Dangerous goods are packed and declared under IMDG or IATA DGR, and the importer's EORI number is needed for customs.
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 Aarhus
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 Denmark
- 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
A selection we ship to Denmark
A rotating sample from the division. Every product in the catalogue can be quoted for this destination.
Questions
Impurity Reference Standards for Denmark
Can Zemixal deliver impurity reference standards to Denmark?
Yes. We ship by sea to Aarhus and Copenhagen, 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 Denmark?
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 Danish Medicines Agency / EMA is agreed with you at quote stage.
How long does delivery to Denmark 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 Denmark
Lab Reagents Solvents (HPLC & GC) Biochemicals APIs Pharmaceutical Intermediates Inorganics & Metals Specialty Chemicals
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