Uruguay · Impurity Reference Standards

Impurity Reference Standards for Uruguay

Zemixal supplies 20,060 products from its impurity reference standards range to buyers in Uruguay. Demand there comes mainly from pulp & paper, meat & dairy processing and pharmaceuticals & veterinary products. Typical delivery points include Montevideo, Fray Bentos and Paso de los Toros. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Uruguay Sample products

20,060products in this division

30–45 dsea transit from India

4–7 dair freight

6categories

Supplying impurity reference standards to Uruguay

Sea freight reaches Montevideo and Nueva Palmira in about 30–45 days port to port. Urgent or small lots fly to Montevideo Carrasco (MVD) in 4–7 days. Import compliance for this category sits with MSP (Ministerio de Salud Pública), 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 Uruguay

Authority	MSP (Ministerio de Salud Pública)
Seaports	Montevideo, Nueva Palmira, Fray Bentos
Airports	Montevideo Carrasco (MVD)
Dangerous goods	IMDG by sea, IATA DGR by air

Medicines and APIs need registration or an import authorisation from the Ministry of Public Health (MSP), so confirm the importer's status before a pharmaceutical order ships. Precursor chemicals require a prior import licence, which the buyer obtains and shares with us so the commercial documents match. If goods enter a free zone or the Montevideo free port for later distribution, tell us at quotation stage so the consignee and paperwork are set up correctly. Dangerous goods are packed and declared under IMDG or IATA rules. Preferential MERCOSUR duty depends on a valid India–MERCOSUR PTA certificate of origin.

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.
30–45 daysOcean transit to Montevideo
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 / MSP (precursor chemicals control).

Indicative total by sea: 37–62 days

By air: about 8–17 days in total.

Documents for Uruguay

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
Certificate of Origin in India–MERCOSUR PTA format for preferential duty
MSP import authorisation for pharmaceuticals where required
Precursor chemical import licence 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 Uruguay

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

Full impurity reference standards range

Dehydro-eletriptan

CAS: 188113-72-6
Formula: C₂₂H₂₄N₂O₂S
MW: 380.5 g/mol

ZX-029208

N-Desmethyl Eletriptan

CAS: 153525-55-4
Formula: C₂₁H₂₄N₂O₂S
MW: 368.5 g/mol

ZX-029209

Eletriptan Rel-3-(R)-1-methylpyrrolidinyl Dimer Impurity

CAS: 2125726-42-1
Formula: C₄₄H₅₀N₄O₄S₂
MW: 763 g/mol

ZX-029210

Eliglustat enantiomer

CAS: 1092472-70-2
Formula: C₂₃H₃₆N₂O₄
MW: 404.5 g/mol

ZX-029211

Eliglustat Phenyl Amino Alcohol Impurity

CAS: 491833-27-3
Formula: C₂₃H₃₀N₂O₄
MW: 398.5 g/mol

ZX-029212

Caprylic acid N-succinimidyl ester

CAS: 14464-30-3
Formula: C₁₂H₁₉NO₄
MW: 241.28 g/mol

ZX-029213

Eliglustat-N-Oxide

CAS: 2137145-62-9
Formula: C₂₃H₃₆N₂O₅
MW: 420.5 g/mol

ZX-029214

N-[(1R,2S)-2-(2,3-Dihydro-1,4-benzodioxin-6-yl)-2-hydroxy-1-(1-pyrrolidinylmethyl)ethyl]-octanamide

CAS: 1092472-66-6
Formula: C₂₃H₃₆N₂O₄
MW: 404.5 g/mol

ZX-029215

N-[(1S,2R)-2-(2,3-Dihydro-1,4-benzodioxin-6-yl)-2-hydroxy-1-(1-pyrrolidinylmethyl)ethyl]octanamide

CAS: 1092472-65-5
Formula: C₂₃H₃₆N₂O₄
MW: 404.5 g/mol

ZX-029216

(1R,2R)-1-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)-2-octanamido-3-(pyrrolidin-1-yl)propyl octanoate

CAS: 2193052-06-9
Formula: C₃₁H₅₀N₂O₅
MW: 530.7 g/mol

ZX-029217

Eliglustat Hexa Analogue

CAS: 2193051-88-4
Formula: C₂₁H₃₂N₂O₄
MW: 376.5 g/mol

ZX-029218

Elinzanetant

CAS: 929046-33-3
Formula: C₃₃H₃₅F₇N₄O₃
MW: 668.6 g/mol

ZX-029219

Questions

Impurity Reference Standards for Uruguay

Can Zemixal deliver impurity reference standards to Uruguay?

Yes. We ship by sea to Montevideo and Nueva Palmira, 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 Uruguay?

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 MSP (Ministerio de Salud Pública) is agreed with you at quote stage.

How long does delivery to Uruguay take?

Allow 30–45 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 Uruguay

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

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