Russia · Impurity Reference Standards

Impurity Standards supply to Russia

Zemixal supplies 20,060 products from its impurity reference standards range to buyers in Russia. Demand there comes mainly from generic pharmaceuticals, petrochemicals & polymers and fertilisers. Regular consignments go to industrial centres such as Moscow & Moscow Oblast, St. Petersburg and Kazan (Tatarstan). Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Russia Sample products

20,060products in this division

30–45 dsea transit from India

4–7 dair freight

6categories

Supplying impurity reference standards to Russia

By sea, containers and LCL lots take roughly 30–45 days to Novorossiysk and St. Petersburg. Air cargo to Moscow Sheremetyevo (SVO) takes 4–7 days, which suits small and urgent packs. The relevant authority is Roszdravnadzor / Ministry of Health (Minzdrav). 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 Russia

Authority	Roszdravnadzor / Ministry of Health (Minzdrav)
Seaports	Novorossiysk, St. Petersburg, Vladivostok
Airports	Moscow Sheremetyevo (SVO), Moscow Domodedovo (DME)
Dangerous goods	IMDG by sea, IATA DGR by air

Chemical products entering Russia must meet Eurasian Economic Union technical regulations, with EAC conformity documents and Russian-language SDS and labels, usually arranged by the importer. APIs for medicines are registered with the Ministry of Health and overseen by Roszdravnadzor. Precursor and narcotic-related substances need specific import licences. Every shipment must be screened against applicable sanctions and export-control lists, and an end-use or end-user statement is typically required. Available shipping and payment routes vary, so terms are confirmed for each order.

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 Novorossiysk
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) / Rospotrebnadzor.

Indicative total by sea: 37–62 days

By air: about 8–17 days in total.

Documents for Russia

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
Russian-language SDS and labelling (usually arranged by importer)
Minzdrav registration details for APIs where applicable
Import licence for precursors where applicable
End-use / end-user statement for sanctions and export-control screening
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 Russia

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

Full impurity reference standards range

Vilazodone Hydrochloride Impurity IV

CAS: 1983197-00-7
Formula: C₂₇H₂₉ClN₄O₃
MW: 493 g/mol

ZX-005519

Vilazodone Impurity 3

CAS: 163521-20-8
Formula: C₁₅H₁₈N₂O₃
MW: 274.31 g/mol

ZX-005520

Vilazodone Impurity IV

CAS: 1236722-93-2
Formula: C₂₇H₂₈N₄O₃
MW: 456.5 g/mol

ZX-005521

Vilazodone Impurity-V (Int-A)

CAS: 183288-47-3
Formula: C₁₃H₁₄N₂O₃
MW: 246.26 g/mol

ZX-005522

Vilazodone Impurity-V (Int-C)

CAS: 276863-95-7
Formula: C₁₃H₁₁ClN₂O
MW: 246.69 g/mol

ZX-005523

Vilazodone N-Boc Acid Impurity

CAS: 1192170-26-5
Formula: C₁₈H₂₂N₂O₅
MW: 346.4 g/mol

ZX-005524

Vilazodone N-Formyl Impurity

CAS: 1602487-82-0
Formula: C₁₄H₁₅N₃O₃
MW: 273.29 g/mol

ZX-005525

Vildagliptin Impurity 2 (S-Isomer)

CAS: 19943-27-2
Formula: C₁₀H₁₄N₂O₂
MW: 194.23 g/mol

ZX-005526

Vildagliptin Impurity-2 [(R and S) Mixture]

CAS: 6708-06-1
Formula: C₁₀H₁₄N₂O₂
MW: 194.23 g/mol

ZX-005527

Vildagliptin L-Proline Impurity

CAS: 674292-94-5
Formula: C₆H₁₁N₃O₂
MW: 157.17 g/mol

ZX-005528

Vismodegib Impurity 5

CAS: 1977536-53-0
Formula: C₂₂H₁₄Cl₂N₄
MW: 405.3 g/mol

ZX-005529

VNL7-VNL5 (Venetoclax Dimer Impurity 2)

CAS: 2270190-88-8
Formula: C₇₈H₈₃Cl₂N₁₁O₉S
MW: 1421.5 g/mol

ZX-005530

Questions

Impurity Reference Standards for Russia

Do you ship impurity standards to Russia?

Yes. We ship by sea to Novorossiysk and St. Petersburg, 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 Russia?

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 Roszdravnadzor / Ministry of Health (Minzdrav) is agreed with you at quote stage.

How long does delivery to Russia take?

Allow 30–45 days for ocean transit or 4–7 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 Russia

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

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