Cyprus · Impurity Reference Standards

Impurity Reference Standards for Cyprus

Buyers in Cyprus can order any of the 20,060 products in our impurity reference standards division. In Cyprus the strongest demand is from generic pharmaceuticals, water desalination & treatment and construction materials. Typical delivery points include Limassol, Nicosia and Larnaca. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Cyprus Sample products

20,060products in this division

16–24 dsea transit from India

3–6 dair freight

6categories

Supplying impurity reference standards to Cyprus

Sea freight reaches Limassol and Larnaca in about 16–24 days port to port. Urgent or small lots fly to Larnaca (LCA) in 3–6 days. Import compliance for this category sits with Cyprus Pharmaceutical Services / 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 Cyprus

Authority	Cyprus Pharmaceutical Services / EMA
Seaports	Limassol, Larnaca
Airports	Larnaca (LCA), Paphos (PFO)
Dangerous goods	IMDG by sea, IATA DGR by air

Cyprus applies EU REACH and CLP. A substance imported at 1 tonne or more per year needs registration by the EU importer or by an Only Representative acting for the Indian manufacturer, and SDS and labels must be in Greek. Active substances for medicines need GMP compliance and an EU written confirmation, with the Cyprus Pharmaceutical Services supervising authorised importers. Dangerous goods are 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.
16–24 daysOcean transit to Limassol
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: 23–41 days

By air: about 7–16 days in total.

Documents for Cyprus

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 Cyprus

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

Full impurity reference standards range

Amiodarone EP Impurity G

CAS: 1087223-70-8
Formula: C₂₆H₃₁I₂NO₄
MW: 675.3 g/mol

ZX-020603

N-Nitroso Amiodarone EP Impurity B

CAS: 678982-38-2
Formula: C₂₃H₂₄I₂N₂O₄
MW: 646.3 g/mol

ZX-020604

N,N-Di-desethyl Amiodarone Hydrochloride

CAS: 757220-04-5
Formula: C₂₁H₂₂ClI₂NO₃
MW: 625.7 g/mol

ZX-020605

Amisulpride EP impurity C

CAS: 176849-91-5
Formula: C₁₅H₂₂IN₃O₂
MW: 403.26 g/mol

ZX-020606

Amitriptyline EP Impurity D

CAS: 1159-03-1
Formula: C₂₀H₂₅NO
MW: 295.4 g/mol

ZX-020607

Nortriptyline EP Impurity J

CAS: 4317-14-0
Formula: C₂₀H₂₃NO
MW: 293.4 g/mol

ZX-020608

Amlodipine Azido Impurity

CAS: 88150-46-3
Formula: C₂₀H₂₃ClN₄O₅
MW: 434.9 g/mol

ZX-020609

Amlodipine N-Lactoside (Mixture of Diastereomers)

CAS: 2173291-00-2
Formula: C₃₂H₄₅ClN₂O₁₅
MW: 733.2 g/mol

ZX-020610

3-O-Desmethyl Amlodipine

CAS: 113994-37-9
Formula: C₁₉H₂₃ClN₂O₅
MW: 394.8 g/mol

ZX-020611

Desethyl Amlodipine

CAS: 1809326-44-0
Formula: C₁₈H₂₁ClN₂O₅
MW: 380.8 g/mol

ZX-020612

N-Formyl Amlodipine

CAS: 93848-81-8
Formula: C₂₁H₂₅ClN₂O₆
MW: 436.9 g/mol

ZX-020613

Amlodipine Related Compound K

CAS: 1621516-91-3
Formula: C₁₈H₂₀ClNO₃
MW: 333.8 g/mol

ZX-020614

Questions

Impurity Reference Standards for Cyprus

Can Zemixal deliver impurity reference standards to Cyprus?

Yes. We ship by sea to Limassol and Larnaca, 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 Cyprus?

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 Cyprus Pharmaceutical Services / EMA is agreed with you at quote stage.

How long does delivery to Cyprus take?

Allow 16–24 days for ocean transit or 3–6 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 Cyprus

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

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