Ukraine · Impurity Reference Standards

Impurity Reference Standards for Ukraine

Buyers in Ukraine can order any of the 20,060 products in our impurity reference standards division. Demand there comes mainly from agrochemicals & fertilisers, generic pharmaceuticals and metallurgy & steel. Regular consignments go to industrial centres such as Kyiv, Kharkiv and Dnipro. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Ukraine Sample products

20,060products in this division

30–45 dsea transit from India

5–8 dair freight

6categories

Supplying impurity reference standards to Ukraine

By sea, containers and LCL lots take roughly 30–45 days to Odesa and Chornomorsk. Air cargo to Rzeszów, Poland (RZE) + road takes 5–8 days, which suits small and urgent packs. The relevant authority is State Service of Ukraine on Medicines and Drugs Control. 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 Ukraine

Authority	State Service of Ukraine on Medicines and Drugs Control
Seaports	Odesa, Chornomorsk, Pivdennyi
Airports	Rzeszów, Poland (RZE) + road, Warsaw, Poland (WAW) + road
Dangerous goods	IMDG by sea, IATA DGR by air

Ukraine is aligning its chemical rules with EU REACH and CLP through national technical regulations, so importers increasingly expect EU-style GHS labelling and SDS content in Ukrainian. Medicinal substances and APIs are overseen by the State Service on Medicines and Drugs Control, and controlled precursors need licences. Cargo is commonly routed through Polish airports or Romanian ports with onward road or rail, using T1 transit documents through the EU. War-risk insurance terms should be agreed before shipment.

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.
30–45 daysOcean transit to Odesa
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: Ministry of Economy / Ministry of Environmental Protection (Ukrainian chemical-safety & CLP-aligned technical regulations).

Indicative total by sea: 37–62 days

By air: about 9–18 days in total.

Documents for Ukraine

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
Ukrainian-language labelling / SDS where required by the buyer or regulation
Import licence or permit for controlled precursors where applicable
Transit/T1 documents when routed through the EU
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 Ukraine

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

Full impurity reference standards range

Cortienic Acid

CAS: 3597-45-3
Formula: C₂₀H₂₈O₅
MW: 348.4 g/mol

ZX-025024

9 Alpha Hydroxyl Hydrocortisone Acetate

CAS: 50733-56-7
Formula: C₂₃H₃₂O₇
MW: 420.5 g/mol

ZX-025025

Epi Hydrocortisone Hemisuccinate

CAS: 103242-89-3
Formula: C₂₅H₃₄O₈
MW: 462.5 g/mol

ZX-025026

Hydrocortisone Glyoxal Hydrate Isomer 1

CAS: 1960421-03-7
Formula: C₂₁H₃₀O₅
MW: 362.5 g/mol

ZX-025027

Delta-9,-11 Hydrocortisone hemisuccinate

CAS: 103497-66-1
Formula: C₂₅H₃₂O₇
MW: 444.5 g/mol

ZX-025028

Cortexolone Hemisuccinate

CAS: 3331-69-9
Formula: C₂₅H₃₄O₇
MW: 446.5 g/mol

ZX-025029

21-Desacetyl Anecortave

CAS: 10184-70-0
Formula: C₂₁H₂₈O₄
MW: 344.4 g/mol

ZX-025030

Hydrocortisone 21-Carboxylic Acid

CAS: 57172-48-2
Formula: C₂₁H₂₈O₆
MW: 376.4 g/mol

ZX-025031

Cortexolone dipropionate

CAS: 19608-30-1
Formula: C₂₇H₃₈O₆
MW: 458.6 g/mol

ZX-025032

Hydroxocobalamin Acetate

CAS: 22465-48-1
Formula: C₆₄H₉₂CoN₁₃O₁₆P-2
MW: 1389.4 g/mol

ZX-025033

Hydroxyethylsalicylate

CAS: 87-28-5
Formula: C₉H₁₀O₄
MW: 182.17 g/mol

ZX-025034

Decloxizine Dihydrochloride

CAS: 13073-96-6
Formula: C₂₁H₃₀Cl₂N₂O₂
MW: 413.4 g/mol

ZX-025035

Questions

Impurity Reference Standards for Ukraine

Do you ship impurity standards to Ukraine?

Yes. We ship by sea to Odesa and Chornomorsk, 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 Ukraine?

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 State Service of Ukraine on Medicines and Drugs Control is agreed with you at quote stage.

How long does delivery to Ukraine take?

Allow 30–45 days for ocean transit or 5–8 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 Ukraine

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

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