Armenia · Impurity Reference Standards

Impurity Standards supply to Armenia

Buyers in Armenia can order any of the 20,060 products in our impurity reference standards division. In Armenia the strongest demand is from generic pharmaceuticals, mining & copper/molybdenum processing and food & brandy production. Regular consignments go to industrial centres such as Yerevan, Gyumri and Vanadzor. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Armenia Sample products

20,060products in this division

35–50 dsea transit from India

3–6 dair freight

6categories

Supplying impurity reference standards to Armenia

By sea, containers and LCL lots take roughly 35–50 days to Poti, Georgia (via road/rail) and Batumi, Georgia (via road). Air cargo to Yerevan Zvartnots (EVN) takes 3–6 days, which suits small and urgent packs. The relevant authority is Scientific Centre of Drug and Medical Technology Expertise (Ministry of Health). 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 Armenia

Authority	Scientific Centre of Drug and Medical Technology Expertise (Ministry of Health)
Seaports	Poti, Georgia (via road/rail), Batumi, Georgia (via road)
Airports	Yerevan Zvartnots (EVN)
Dangerous goods	IMDG by sea, IATA DGR by air

Armenia is a member of the Eurasian Economic Union and applies its technical regulations and customs rules. Some chemical products need EAC conformity documents and Armenian or Russian labelling, arranged by the importer. APIs and medicines are evaluated by the Scientific Centre of Drug and Medical Technology Expertise under the Ministry of Health. Precursors and narcotic substances need import permits. Sea cargo reaches Armenia through Poti or Batumi under a transit declaration, 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.
35–50 daysOcean transit to Poti, Georgia (via road/rail)
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 Economy.

Indicative total by sea: 42–67 days

By air: about 7–16 days in total.

Documents for Armenia

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
EAEU/EAC conformity document where applicable
Transit declaration via Georgia
Import permit for precursors or narcotic substances 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 Armenia

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

Full impurity reference standards range

N-Desmethyl Danofloxacin

CAS: 108461-04-7
Formula: C₁₈H₁₈FN₃O₃
MW: 343.4 g/mol

ZX-028815

Danofloxacin

CAS: 112398-08-0
Formula: C₁₉H₂₀FN₃O₃
MW: 357.4 g/mol

ZX-028816

Dantrolene

CAS: 7261-97-4
Formula: C₁₄H₁₀N₄O₅
MW: 314.25 g/mol

ZX-028817

Dantrolene, Sodium Salt Hemiheptahydrate

CAS: 24868-20-0
Formula: C₂₈H₃₂N₈Na₂O₁₇
MW: 798.6 g/mol

ZX-028818

Aminodantrolene

CAS: 14663-28-6
Formula: C₁₄H₁₂N₄O₃
MW: 284.27 g/mol

ZX-028819

5-Hydroxy Dantrolene

CAS: 52130-25-3
Formula: C₁₄H₁₀N₄O₆
MW: 330.25 g/mol

ZX-028820

Dithranol EP Impurity B

CAS: 117-10-2
Formula: C₁₄H₈O₄
MW: 240.21 g/mol

ZX-028821

(3R,4S,5S,6R)-6-((((2S,3R,4S,5S,6R)-2-(4-Chloro-3-(4-ethoxybenzyl)phenyl)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)methyl)-3,4,5-trihydroxytetrahydro-2H-pyran-2-one

CAS: 2452300-92-2
Formula: C₂₇H₃₃ClO₁₂
MW: 585 g/mol

ZX-028822

Dapagliflozin (RS) Furanose

CAS: 2271248-78-1
Formula: C₂₁H₂₅ClO₆
MW: 408.9 g/mol

ZX-028823

1-Chloro-2-(4-ethoxybenzyl)-4-iodobenzene

CAS: 1103738-29-9
Formula: C₁₅H₁₄ClIO
MW: 372.63 g/mol

ZX-028824

Dapagliflozin Allose Isomer

CAS: 1888296-95-4
Formula: C₂₁H₂₅ClO₆
MW: 408.9 g/mol

ZX-028825

Galacto-Dapagliflozin

CAS: 1408245-02-2
Formula: C₂₁H₂₅ClO₆
MW: 408.9 g/mol

ZX-028826

Questions

Impurity Reference Standards for Armenia

Do you ship impurity standards to Armenia?

Yes. We ship by sea to Poti, Georgia (via road/rail) and Batumi, Georgia (via road), 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 Armenia?

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 Scientific Centre of Drug and Medical Technology Expertise (Ministry of Health) is agreed with you at quote stage.

How long does delivery to Armenia take?

Allow 35–50 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 Armenia

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

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