Montenegro · Impurity Reference Standards

Impurity Reference Standards for Montenegro

Zemixal supplies 20,060 products from its impurity reference standards range to buyers in Montenegro. Demand there comes mainly from aluminium & metals processing, water treatment and hospitals & pharmacy supply. Typical delivery points include Podgorica, Bar and Nikšić. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Montenegro Sample products

20,060products in this division

25–35 dsea transit from India

4–7 dair freight

6categories

Supplying impurity reference standards to Montenegro

Sea freight reaches Bar and Kotor in about 25–35 days port to port. Urgent or small lots fly to Podgorica (TGD) in 4–7 days. Import compliance for this category sits with CInMED (Institute for Medicines and Medical Devices of Montenegro), 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 Montenegro

Authority	CInMED (Institute for Medicines and Medical Devices of Montenegro)
Seaports	Bar, Kotor
Airports	Podgorica (TGD), Tivat (TIV)
Dangerous goods	IMDG by sea, IATA DGR by air

Montenegro is an EU candidate and has adopted chemicals legislation modelled on REACH and CLP. Imports of hazardous chemicals are generally notified or registered with the national environmental authority by the local importer, who also prepares the Montenegrin-language SDS. Medicinal substances fall under CInMED, the Institute for Medicines and Medical Devices. Controlled precursors need import permits before shipment. Dangerous goods must be declared under IMDG or IATA rules, and the euro is used as the national currency.

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.
25–35 daysOcean transit to Bar
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: Environmental Protection Agency of Montenegro (chemicals law aligned with EU REACH/CLP).

Indicative total by sea: 32–52 days

By air: about 8–17 days in total.

Documents for Montenegro

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
Montenegrin-language SDS (prepared by the importer)
Import permit for precursor or controlled chemicals 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 Montenegro

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

Full impurity reference standards range

Risperidone EP Impurity F

CAS: 1346603-86-8
Formula: C₂₄H₂₇FN₄O₄
MW: 454.5 g/mol

ZX-026743

cis-Risperidone N-Oxide

CAS: 1894509-66-0
Formula: C₂₃H₂₇FN₄O₃
MW: 426.5 g/mol

ZX-026744

(R)-9-Hydroxy Risperidone

CAS: 130049-85-3
Formula: C₂₃H₂₇FN₄O₃
MW: 426.5 g/mol

ZX-026745

Risperidone Degradation Product

CAS: 832747-59-8
Formula: C₁₁H₁₄N₂O
MW: 190.24 g/mol

ZX-026746

Risperidone Hydroxyethyl Impurity

CAS: 66698-27-9
Formula: C₁₁H₁₆N₂O₂
MW: 208.26 g/mol

ZX-026747

(2R,5S)-Ritlecitinib

CAS: 1792180-79-0
Formula: C₁₅H₁₉N₅O
MW: 285.34 g/mol

ZX-026748

Ritonavir EP Impurity Q

CAS: 1414933-82-6
Formula: C₃₇H₄₈N₆O₅S₂
MW: 720.9 g/mol

ZX-026749

Ritonavir EP Impurity S

CAS: 2084828-53-3
Formula: C₅₂H₆₁N₇O₈S₂
MW: 976.2 g/mol

ZX-026750

(S)-2-(3-((2-Isopropylthiazol-4-yl)methyl)-3-methylureido)butanoic acid

CAS: 1004316-34-0
Formula: C₁₃H₂₁N₃O₃S
MW: 299.39 g/mol

ZX-026751

Rivaroxaban EP Impurity J

CAS: 1632463-24-1
Formula: C₃₈H₃₆Cl₂N₆O₁₀S₂
MW: 871.8 g/mol

ZX-026752

4,5-Dichlorothiophene-2-carboxylic Acid

CAS: 31166-29-7
Formula: C₅H₂Cl₂O₂S
MW: 197.04 g/mol

ZX-026753

2-[2-[[4-[(5S)-5-[[[(5-Chloro-2-thienyl)carbonyl]amino]methyl]-2-oxo-3-oxazolidinyl]phenyl]amino]ethoxy]-acetic Acid Hydrochloride

CAS: 931117-61-2
Formula: C₁₉H₂₁Cl₂N₃O₆S
MW: 490.4 g/mol

ZX-026754

Questions

Impurity Reference Standards for Montenegro

Can Zemixal deliver impurity reference standards to Montenegro?

Yes. We ship by sea to Bar and Kotor, 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 Montenegro?

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 CInMED (Institute for Medicines and Medical Devices of Montenegro) is agreed with you at quote stage.

How long does delivery to Montenegro take?

Allow 25–35 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 Montenegro

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

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