Kazakhstan · Impurity Reference Standards

Impurity Standards supply to Kazakhstan

Zemixal supplies 20,060 products from its impurity reference standards range to buyers in Kazakhstan. Demand there comes mainly from oil, gas & petrochemicals, mining & metallurgy (uranium, copper, zinc) and generic pharmaceuticals. Typical delivery points include Almaty, Astana and Shymkent. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Kazakhstan Sample products

20,060products in this division

40–55 dsea transit from India

3–6 dair freight

6categories

Supplying impurity reference standards to Kazakhstan

Sea freight reaches Aktau (Caspian) and Poti, Georgia (via Caspian ferry/rail) in about 40–55 days port to port. Urgent or small lots fly to Almaty (ALA) in 3–6 days. Import compliance for this category sits with National Center for Expertise of Medicines (NCELS) / Ministry of Healthcare, 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 Kazakhstan

Authority	National Center for Expertise of Medicines (NCELS) / Ministry of Healthcare
Seaports	Aktau (Caspian), Poti, Georgia (via Caspian ferry/rail), Lianyungang, China (via rail)
Airports	Almaty (ALA), Astana (NQZ)
Dangerous goods	IMDG by sea, IATA DGR by air

Kazakhstan applies Eurasian Economic Union technical regulations and the common customs tariff. Certain chemical products need EAC conformity documents and Kazakh or Russian labelling, usually arranged by the importer. APIs and medicines are registered through the National Center for Expertise of Medicines (NCELS), which normally expects GMP evidence. Precursors require licences. Multimodal routing via Caspian, Georgian or Chinese gateways needs rail and transit documents such as CIM or SMGS, and dangerous goods follow IMDG or IATA.

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.
40–55 daysOcean transit to Aktau (Caspian)
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: EAEU technical regulations (EAC) / Ministry of Industry and Construction.

Indicative total by sea: 47–72 days

By air: about 7–16 days in total.

Documents for Kazakhstan

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
EAEU/EAC declaration or certificate of conformity where applicable
Kazakh/Russian-language labelling (arranged by importer)
NCELS registration details for APIs where applicable
Precursor import licence where applicable
Rail/transit documents (CIM/SMGS) for multimodal routing
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 Kazakhstan

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

Full impurity reference standards range

Cetirizine Glycerol Ester Impurity

CAS: 1243652-36-9
Formula: C₂₄H₃₁ClN₂O₅
MW: 463 g/mol

ZX-004513

Cetirizine Impurity B (Dihydrochloride)

CAS: 1000690-91-4
Formula: C₁₉H₂₃Cl₃N₂O₂
MW: 417.8 g/mol

ZX-004514

Cetirizine Impurity D (Dihydrochloride)

CAS: 856841-95-7
Formula: C₃₀H₂₈Cl₂N₂
MW: 487.5 g/mol

ZX-004515

Cetirizine Impurity E (Dihydrochloride)

CAS: 83881-56-5
Formula: C₂₃H₃₁Cl₃N₂O₄
MW: 505.9 g/mol

ZX-004516

Cetirizine Impurity F

CAS: 83881-53-2
Formula: C₂₁H₂₆N₂O₃
MW: 354.4 g/mol

ZX-004517

Cetirizine Impurity F (Dihydrochloride)

CAS: 83881-54-3
Formula: C₂₁H₂₈Cl₂N₂O₃
MW: 427.4 g/mol

ZX-004518

Cetirizine Methyl Ester Impurity

CAS: 83881-46-3
Formula: C₂₂H₂₇ClN₂O₃
MW: 402.9 g/mol

ZX-004519

Chlormadinone Acetate (Reference Standard)

CAS: 302-22-7
Formula: C₂₃H₂₉ClO₄
MW: 404.9 g/mol

ZX-004520

Chloro Propanyl Dimer Impurity of Ibrutinib (PCI-7547)

CAS: 2031255-23-7
Formula: C₅₀H₄₈N₁₂O₄
MW: 881 g/mol

ZX-004521

Cholesterol Impurity 11

CAS: 14214-69-8
Formula: C₂₇H₄₄O
MW: 384.6 g/mol

ZX-004522

Cinacalcet Impurity 31

CAS: 1034094-54-6
Formula: C₁₀H₉F₃O
MW: 202.17 g/mol

ZX-004523

Cinacalcet Impurity A

CAS: 3886-70-2
Formula: C₁₂H₁₃N
MW: 171.24 g/mol

ZX-004524

Questions

Impurity Reference Standards for Kazakhstan

Can Zemixal deliver impurity reference standards to Kazakhstan?

Yes. We ship by sea to Aktau (Caspian) and Poti, Georgia (via Caspian ferry/rail), 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 Kazakhstan?

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 National Center for Expertise of Medicines (NCELS) / Ministry of Healthcare is agreed with you at quote stage.

How long does delivery to Kazakhstan take?

Allow 40–55 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 Kazakhstan

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

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