Turkey · Impurity Reference Standards

Impurity Reference Standards shipped to Turkey

The impurity reference standards division counts 20,060 products, and each one can be quoted for delivery to Turkey. Locally, the main users are in generic pharmaceuticals, textiles & dyeing and automotive & coatings. Typical delivery points include Istanbul, Kocaeli (Gebze/Dilovası chemical zone) and Tekirdağ (Çerkezköy). Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Turkey Sample products

20,060products in this division

18–26 dsea transit from India

2–4 dair freight

6categories

Supplying impurity reference standards to Turkey

Sea freight reaches Ambarlı (Istanbul) and Mersin in about 18–26 days port to port. Urgent or small lots fly to Istanbul (IST) in 2–4 days. Import compliance for this category sits with TİTCK (Turkish Medicines and Medical Devices Agency), 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 Turkey

Authority	TİTCK (Turkish Medicines and Medical Devices Agency)
Seaports	Ambarlı (Istanbul), Mersin, Gebze / Izmit (Kocaeli)
Airports	Istanbul (IST), Istanbul Sabiha Gökçen (SAW)
Dangerous goods	IMDG by sea, IATA DGR by air

Turkey's KKDIK regulation mirrors EU REACH. Substances placed on the Turkish market at 1 tonne or more per year must be registered by the Turkish manufacturer, the importer or an Only Representative, with phased deadlines. SDS must be prepared in Turkish by a certified SDS preparer, which the importer usually arranges. APIs and medicines fall under TİTCK, which generally expects GMP evidence for the manufacturing site. Dangerous goods move under IMDG or IATA rules.

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.
18–26 daysOcean transit to Ambarlı (Istanbul)
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: KKDIK (Ministry of Environment, Urbanisation and Climate Change).

Indicative total by sea: 25–43 days

By air: about 6–14 days in total.

Documents for Turkey

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
KKDIK registration / pre-registration number or OR declaration (substances ≥1 t/yr)
Turkish-language SDS prepared by a certified SDS preparer (usually arranged by importer)
TİTCK-related API documentation (e.g. GMP evidence, DMF) 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 Turkey

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

Full impurity reference standards range

2-Methyl-5H-dibenzazepine

CAS: 70401-31-9
Formula: C₁₅H₁₃N
MW: 207.27 g/mol

ZX-032812

2,5-Dimethyl Celecoxib

CAS: 457639-26-8
Formula: C₁₈H₁₆F₃N₃O₂S
MW: 395.4 g/mol

ZX-032813

Ethyl Ester of Cetirizine Dihydrochloride

CAS: 2732277-01-7
Formula: C₂₃H₃₁Cl₃N₂O₃
MW: 489.9 g/mol

ZX-032814

1,1-Dimethyl-3-cyanoguanidine

CAS: 1609-06-9
Formula: C₄H₈N₄
MW: 112.13 g/mol

ZX-032815

5-Acetyl-10,11-dihydro-5H-dibenzo[b,f]azepine

CAS: 13080-75-6
Formula: C₁₆H₁₅NO
MW: 237.3 g/mol

ZX-032816

Cyclizine Hydrochloride

CAS: 303-25-3
Formula: C₁₈H₂₃ClN₂
MW: 302.8 g/mol

ZX-032817

Didanosine

CAS: 69655-05-6
Formula: C₁₀H₁₂N₄O₃
MW: 236.23 g/mol

ZX-032818

Dithranol

CAS: 1143-38-0
Formula: C₁₄H₁₀O₃
MW: 226.23 g/mol

ZX-032819

Fipronil Sulfone

CAS: 120068-36-2
Formula: C₁₂H₄Cl₂F₆N₄O₂S
MW: 453.1 g/mol

ZX-032820

Flubendazole EP Impurity C

CAS: 1097107-40-8
Formula: C₁₄H₉FN₂O₂
MW: 256.23 g/mol

ZX-032821

Flubendazole EP Impurity D

CAS: 1515807-30-3
Formula: C₁₄H₉FN₂O
MW: 240.23 g/mol

ZX-032822

Flucloxacillin Sodium

CAS: 1847-24-1
Formula: C₁₉H₁₆ClFN₃NaO₅S
MW: 475.9 g/mol

ZX-032823

Questions

Impurity Reference Standards for Turkey

Can Zemixal deliver impurity reference standards to Turkey?

Yes. We ship by sea to Ambarlı (Istanbul) and Mersin, 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 Turkey?

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 TİTCK (Turkish Medicines and Medical Devices Agency) is agreed with you at quote stage.

How long does delivery to Turkey take?

Allow 18–26 days for ocean transit or 2–4 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 Turkey

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

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