Azerbaijan · Impurity Reference Standards

Impurity Reference Standards shipped to Azerbaijan

Buyers in Azerbaijan can order any of the 20,060 products in our impurity reference standards division. In Azerbaijan the strongest demand is from oil & gas and petrochemicals, refining & polymers and water treatment. Regular consignments go to industrial centres such as Baku, Sumgait Chemical Industrial Park and Ganja. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Azerbaijan Sample products

20,060products in this division

35–50 dsea transit from India

3–5 dair freight

6categories

Supplying impurity reference standards to Azerbaijan

By sea, containers and LCL lots take roughly 35–50 days to Baku International Sea Trade Port (Alat, Caspian) and Poti, Georgia (via rail). Air cargo to Baku Heydar Aliyev (GYD) takes 3–5 days, which suits small and urgent packs. The relevant authority is Analytical Expertise Centre (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 Azerbaijan

Authority	Analytical Expertise Centre (Ministry of Health)
Seaports	Baku International Sea Trade Port (Alat, Caspian), Poti, Georgia (via rail), Batumi, Georgia (via rail)
Airports	Baku Heydar Aliyev (GYD)
Dangerous goods	IMDG by sea, IATA DGR by air

Chemical imports into Azerbaijan are cleared by the State Customs Committee, and hazardous or controlled substances can require permits from the relevant ministries. SDS and labels in Azerbaijani or Russian are commonly requested, and the importer usually prepares them. Pharmaceutical substances are assessed by the Analytical Expertise Centre of the Ministry of Health. Sea freight normally arrives through Georgian Black Sea ports with rail onward to Baku, or via Alat. Dangerous goods follow 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.
35–50 daysOcean transit to Baku International Sea Trade Port (Alat, 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: Ministry of Ecology and Natural Resources / State Customs Committee.

Indicative total by sea: 42–67 days

By air: about 7–15 days in total.

Documents for Azerbaijan

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
Azerbaijani/Russian-language labelling or SDS where requested
Permit for controlled or hazardous substances where applicable
Transit documents via Georgia
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 Azerbaijan

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

Full impurity reference standards range

Glibenclamide EP Impurity B

CAS: 21165-77-5
Formula: C₁₈H₁₉ClN₂O₆S
MW: 426.9 g/mol

ZX-021787

Glibenclamide EP Impurity E

CAS: 57334-89-1
Formula: C₂₃H₂₇Cl₂N₃O₅S
MW: 528.4 g/mol

ZX-021788

Gliclazide EP Impurity C

CAS: 5577-13-9
Formula: C₁₀H₁₃NO₄S
MW: 243.28 g/mol

ZX-021789

Gliclazide EP Impurity D

CAS: 1136426-19-1
Formula: C₁₅H₂₀N₂O₃S
MW: 308.4 g/mol

ZX-021790

Glimepiride EP Impurity A

CAS: 684286-46-2
Formula: C₂₄H₃₄N₄O₅S
MW: 490.6 g/mol

ZX-021791

Glimepiride EP Impurity B

CAS: 119018-29-0
Formula: C₁₆H₂₁N₃O₄S
MW: 351.4 g/mol

ZX-021792

Glimepiride EP Impurity E

CAS: 2366968-77-4
Formula: C₁₆H₂₁N₃O₄S
MW: 351.4 g/mol

ZX-021793

Glimepiride Ethyl Ester Impurity

CAS: 318515-70-7
Formula: C₁₉H₂₅N₃O₆S
MW: 423.5 g/mol

ZX-021794

Glimepiride EP Impurity H

CAS: 2724503-28-8
Formula: C₂₄H₂₈N₄O₅S
MW: 484.6 g/mol

ZX-021795

Glimepiride EP Impurity J

CAS: 41176-98-1
Formula: C₁₆H₂₅N₃O₃S
MW: 339.5 g/mol

ZX-021796

Glucosamine EP Impurity B

CAS: 13185-73-4
Formula: C₁₂H₂₀N₂O₈
MW: 320.3 g/mol

ZX-021797

Granisetron EP Impurity A

CAS: 127472-42-8
Formula: C₁₈H₂₄N₄O
MW: 312.4 g/mol

ZX-021798

Questions

Impurity Reference Standards for Azerbaijan

Do you ship impurity standards to Azerbaijan?

Yes. We ship by sea to Baku International Sea Trade Port (Alat, Caspian) and Poti, Georgia (via 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 Azerbaijan?

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 Analytical Expertise Centre (Ministry of Health) is agreed with you at quote stage.

How long does delivery to Azerbaijan take?

Allow 35–50 days for ocean transit or 3–5 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 Azerbaijan

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

Impurity Reference Standards in nearby countries