Moldova · Impurity Reference Standards

Impurity Reference Standards for Moldova

The impurity reference standards division counts 20,060 products, and each one can be quoted for delivery to Moldova. Locally, the main users are in wine & food processing, generic pharmaceuticals and agriculture & agrochemicals. Typical delivery points include Chișinău, Bălți and Giurgiulești Free International Port. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Moldova Sample products

20,060products in this division

30–42 dsea transit from India

4–7 dair freight

6categories

Supplying impurity reference standards to Moldova

Sea freight reaches Constanța, Romania (via road/rail) and Giurgiulești (Danube) in about 30–42 days port to port. Urgent or small lots fly to Chișinău (RMO) in 4–7 days. Import compliance for this category sits with Medicines and Medical Devices Agency (AMDM), and we prepare the COA, SDS and commercial documents your broker needs. 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 Moldova

Authority	Medicines and Medical Devices Agency (AMDM)
Seaports	Constanța, Romania (via road/rail), Giurgiulești (Danube), Odesa, Ukraine (when open)
Airports	Chișinău (RMO), Iași, Romania (IAS) + road
Dangerous goods	IMDG by sea, IATA DGR by air

Moldova, an EU candidate, has a chemicals law modelled on EU CLP principles, and importers are expected to hold compliant SDS and labelling in Romanian. Medicines and APIs need authorisation from AMDM, the Medicines and Medical Devices Agency. Narcotic and precursor substances require separate permits held by the buyer. Most sea cargo arrives via Constanța or the Giurgiulești Danube terminal with road haulage onward, and dangerous goods must be declared under 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.
30–42 daysOcean transit to Constanța, Romania (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: Ministry of Environment (Law on Chemicals, EU-aligned).

Indicative total by sea: 37–59 days

By air: about 8–17 days in total.

Documents for Moldova

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
Romanian-language labelling / SDS where required
AMDM import authorisation for medicinal substances where applicable
Precursor import permit 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 Moldova

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

Full impurity reference standards range

Mesosulfuron-methyl

CAS: 208465-21-8
Formula: C₁₇H₂₁N₅O₉S₂
MW: 503.5 g/mol

ZX-031351

Etofenprox

CAS: 80844-07-1
Formula: C₂₅H₂₈O₃
MW: 376.5 g/mol

ZX-031352

7-Methylindoline-2,3-dione

CAS: 1127-59-9
Formula: C₉H₇NO₂
MW: 161.16 g/mol

ZX-031353

N-Phenyldiethanolamine

CAS: 120-07-0
Formula: C₁₀H₁₅NO₂
MW: 181.23 g/mol

ZX-031354

DL-5-Hydroxy-DL-lysine Hydrochloride

CAS: 13204-98-3
Formula: C₆H₁₅ClN₂O₃
MW: 198.65 g/mol

ZX-031355

2-Amino-6-mercaptopurine-9-D-riboside Hydrate

CAS: 345909-25-3
Formula: C₁₀H₁₅N₅O₅S
MW: 317.32 g/mol

ZX-031356

6-Mercaptopurine-9-beta-D-Ribofuranoside

CAS: 574-25-4
Formula: C₁₀H₁₂N₄O₄S
MW: 284.29 g/mol

ZX-031357

N-Nitroso Indoline

CAS: 7633-57-0
Formula: C₈H₈N₂O
MW: 148.16 g/mol

ZX-031358

N-Ethyl-N-(2-hydroxyethyl)nitrosamine

CAS: 13147-25-6
Formula: C₄H₁₀N₂O₂
MW: 118.13 g/mol

ZX-031359

1H-Pyrazole-3-carboxamide, 5-Bromo-N-methyl

CAS: 1328893-13-5
Formula: C₅H₆BrN₃O
MW: 204.02 g/mol

ZX-031360

3-Deschloro-4-methyl-Chlorantraniliprole

CAS: 500007-36-3
Formula: C₁₈H₁₅BrClN₅O₂
MW: 448.7 g/mol

ZX-031361

Ascorbyl Glucoside

CAS: 129499-78-1
Formula: C₁₂H₁₈O₁₁
MW: 338.26 g/mol

ZX-031362

Questions

Impurity Reference Standards for Moldova

Can Zemixal deliver impurity reference standards to Moldova?

Yes. We ship by sea to Constanța, Romania (via road/rail) and Giurgiulești (Danube), 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 Moldova?

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 Medicines and Medical Devices Agency (AMDM) is agreed with you at quote stage.

How long does delivery to Moldova take?

Allow 30–42 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 Moldova

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

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