Greece · Impurity Reference Standards

Impurity Reference Standards for Greece

The impurity reference standards division counts 20,060 products, and each one can be quoted for delivery to Greece. In Greece the strongest demand is from generic pharmaceuticals, refining & petrochemicals and aluminium. Regular consignments go to industrial centres such as Attica (Athens), Thessaloniki and Oinofyta (Viotia). Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Greece Sample products

20,060products in this division

14–20 dsea transit from India

3–5 dair freight

6categories

Supplying impurity reference standards to Greece

By sea, containers and LCL lots take roughly 14–20 days to Piraeus and Thessaloniki. Air cargo to Athens (ATH) takes 3–5 days, which suits small and urgent packs. The relevant authority is EOF / 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 Greece

Authority	EOF / EMA
Seaports	Piraeus, Thessaloniki
Airports	Athens (ATH), Thessaloniki (SKG)
Dangerous goods	IMDG by sea, IATA DGR by air

Greece applies EU REACH and CLP. Substances imported at 1 tonne or more per year require registration by the EU importer or by an Only Representative for the Indian manufacturer, and SDS and labels must be in Greek. Active substances for medicinal products need GMP compliance and an EU written confirmation, and EOF supervises authorised importers. Dangerous goods are packed and declared under IMDG or IATA DGR, and customs clearance requires 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.
14–20 daysOcean transit to Piraeus
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: 21–37 days

By air: about 7–15 days in total.

Documents for Greece

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 Greece

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

Full impurity reference standards range

Stigmastan-3β-ol

CAS: 19466-47-8
Formula: C₂₉H₅₂O
MW: 416.7 g/mol

ZX-042515

Sulconazole Nitrate

CAS: 61318-91-0
Formula: C₁₈H₁₆Cl₃N₃O₃S
MW: 460.8 g/mol

ZX-042522

Sulfamethizole-13C6

CAS: 1334378-92-5
Formula: C₉H₁₀N₄O₂S₂
MW: 276.3 g/mol

ZX-042525

Sulfapyridine 13C6

CAS: 1228182-45-3
Formula: C₁₁H₁₁N₃O₂S
MW: 255.25 g/mol

ZX-042527

Sulfathiazole Sodium Salt

CAS: 144-74-1
Formula: C₉H₈N₃NaO₂S₂
MW: 277.3 g/mol

ZX-042528

Suvorexant Impurity 10

CAS: 51793-93-2
Formula: C₇H₄ClNOS
MW: 185.63 g/mol

ZX-042533

(3S,4S,5R)-3-(3,4-Difluoro-2-methoxyphenyl)-4,5-dimethyl-5-(trifluoromethyl)dihydrofuran-2(3H)-one

CAS: 2875066-38-7
Formula: C₁₄H₁₃F₅O₃
MW: 324.24 g/mol

ZX-042534

2-Phenyl-1,3-benzoxazole-6-carboxylic acid

CAS: 594839-90-4
Formula: C₁₄H₉NO₃
MW: 239.23 g/mol

ZX-042535

Tafenoquine Succinate

CAS: 106635-81-8
Formula: C₂₈H₃₄F₃N₃O₇
MW: 581.6 g/mol

ZX-042536

2-(4-Oxopentyl)isoindoline-1,3-dione

CAS: 3197-25-9
Formula: C₁₃H₁₃NO₃
MW: 231.25 g/mol

ZX-042537

1,2-Diphenyl-1-(4-hydroxyphenyl)but-1-ene

CAS: 68684-63-9
Formula: C₂₂H₂₀O
MW: 300.4 g/mol

ZX-042538

1,2-Diphenylbutan-1-one

CAS: 16282-16-9
Formula: C₁₆H₁₆O
MW: 224.3 g/mol

ZX-042539

Questions

Impurity Reference Standards for Greece

Do you ship impurity standards to Greece?

Yes. We ship by sea to Piraeus and Thessaloniki, 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 Greece?

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 EOF / EMA is agreed with you at quote stage.

How long does delivery to Greece take?

Allow 14–20 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 Greece

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

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