Turkmenistan · Impurity Reference Standards

Impurity Reference Standards shipped to Turkmenistan

The impurity reference standards division counts 20,060 products, and each one can be quoted for delivery to Turkmenistan. In Turkmenistan the strongest demand is from natural gas & gas chemicals, oil refining and fertilisers (urea, ammonia). Regular consignments go to industrial centres such as Ashgabat, Turkmenbashi and Mary. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Turkmenistan Sample products

20,060products in this division

40–55 dsea transit from India

4–7 dair freight

6categories

Supplying impurity reference standards to Turkmenistan

By sea, containers and LCL lots take roughly 40–55 days to Turkmenbashi (Caspian) and Poti, Georgia (via Caspian ferry). Air cargo to Ashgabat (ASB) takes 4–7 days, which suits small and urgent packs. The relevant authority is Ministry of Health and Medical Industry. 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 Turkmenistan

Authority	Ministry of Health and Medical Industry
Seaports	Turkmenbashi (Caspian), Poti, Georgia (via Caspian ferry), Baku/Alat, Azerbaijan (via Caspian ferry)
Airports	Ashgabat (ASB)
Dangerous goods	IMDG by sea, IATA DGR by air

Imports into Turkmenistan are closely managed. Contracts are often registered with the State Commodity and Raw Materials Exchange before goods can move, and hazardous chemicals may need permits from the relevant ministries. Pharmaceutical substances fall under the Ministry of Health and Medical Industry. Sea cargo usually reaches Turkmenbashi via Georgian ports and a trans-Caspian ferry, so transit documents are part of the file. Hard-currency payment arrangements should be confirmed in advance, 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 Turkmenbashi (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 Environmental Protection / State Customs Service.

Indicative total by sea: 47–72 days

By air: about 8–17 days in total.

Documents for Turkmenistan

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
Contract registration with the State Commodity and Raw Materials Exchange where applicable
Permit for hazardous or controlled substances where applicable
Transit documents via Georgia/Azerbaijan
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 Turkmenistan

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

Full impurity reference standards range

Phenylephrine Bitartrate

CAS: 17162-39-9
Formula: C₁₃H₁₉NO₈
MW: 317.29 g/mol

ZX-042465

DL-Phenylephrine Hydrochloride

CAS: 154-86-9
Formula: C₉H₁₄ClNO₂
MW: 203.66 g/mol

ZX-042466

3-Chloromethyl-5-methylpyridine Hydrochloride

CAS: 1007089-84-0
Formula: C₇H₉Cl₂N
MW: 178.06 g/mol

ZX-042469

Rutin Hydrate

CAS: 207671-50-9
Formula: C₂₇H₃₆O₁₉
MW: 664.6 g/mol

ZX-042471

4-Methyl-7H-pyrrolo[2,3-d]pyrimidine

CAS: 945950-37-8
Formula: C₇H₇N₃
MW: 133.15 g/mol

ZX-042472

4-Hydroxy-3-(hydroxymethyl)benzoic acid

CAS: 82885-62-9
Formula: C₈H₈O₄
MW: 168.15 g/mol

ZX-042474

alpha-Santalol

CAS: 115-71-9
Formula: C₁₅H₂₄O
MW: 220.35 g/mol

ZX-042478

2,4-Diamino-6-hydroxy-5-nitrosopyrimidine

CAS: 2387-48-6
Formula: C₄H₅N₅O₂
MW: 155.12 g/mol

ZX-042479

Secobarbital

CAS: 76-73-3
Formula: C₁₂H₁₈N₂O₃
MW: 238.28 g/mol

ZX-042484

Sedaxane

CAS: 874967-67-6
Formula: C₁₈H₁₉F₂N₃O
MW: 331.4 g/mol

ZX-042486

Selegiline EP Impurity B

CAS: 156-34-3
Formula: C₉H₁₃N
MW: 135.21 g/mol

ZX-042488

Selumetinib Impurity 24

CAS: 774608-49-0
Formula: C₆H₃BrClI
MW: 317.35 g/mol

ZX-042489

Questions

Impurity Reference Standards for Turkmenistan

Do you ship impurity standards to Turkmenistan?

Yes. We ship by sea to Turkmenbashi (Caspian) and Poti, Georgia (via Caspian ferry), 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 Turkmenistan?

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 Ministry of Health and Medical Industry is agreed with you at quote stage.

How long does delivery to Turkmenistan take?

Allow 40–55 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 Turkmenistan

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

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