Mauritius · Impurity Reference Standards

Impurity Standards supply to Mauritius

The impurity reference standards division counts 20,060 products, and each one can be quoted for delivery to Mauritius. Locally, the main users are in textiles and apparel, sugar and food processing and pharmaceutical and nutraceutical formulation. Regular consignments go to industrial centres such as Port Louis, Plaine Lauzun and Riche Terre. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Mauritius Sample products

20,060products in this division

12–18 dsea transit from India

3–5 dair freight

6categories

Supplying impurity reference standards to Mauritius

By sea, containers and LCL lots take roughly 12–18 days to Port Louis. Air cargo to Sir Seewoosagur Ramgoolam (MRU) takes 3–5 days, which suits small and urgent packs. The relevant authority is Pharmacy Board (Ministry of Health and Wellness). 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 Mauritius

Authority	Pharmacy Board (Ministry of Health and Wellness)
Seaports	Port Louis
Airports	Sir Seewoosagur Ramgoolam (MRU)
Dangerous goods	IMDG by sea, IATA DGR by air

Under the Dangerous Chemicals Control Act, importers of listed dangerous chemicals need a licence and a permit for each consignment from the Dangerous Chemicals Control Board. Apply for the permit before the goods leave India. Pharmaceuticals and APIs require Pharmacy Board registration and import authorisation. To claim the CECPA tariff preference, request the certificate of origin when you place the order, as it must be issued at the time of export. 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.
12–18 daysOcean transit to Port Louis
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: Dangerous Chemicals Control Board (Ministry of Health and Wellness).

Indicative total by sea: 19–35 days

By air: about 7–15 days in total.

Documents for Mauritius

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
Dangerous Chemicals Control Board import permit where applicable
Pharmacy Board import authorisation for APIs and medicines
CECPA Certificate of Origin for preferential duty
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 Mauritius

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

Full impurity reference standards range

Roxadustat Impurity 7

CAS: 2244489-54-9
Formula: C₁₈H₁₅NO₅
MW: 325.3 g/mol

ZX-005305

Roxithromycin Impurity - G

CAS: 425365-64-6
Formula: C₄₂H₇₈N₂O₁₆
MW: 867.1 g/mol

ZX-005306

Rucaparib Impurity 13

CAS: 283173-84-2
Formula: C₁₈H₁₃FN₂O₂
MW: 308.3 g/mol

ZX-005307

Rucaparib Impurity 16

CAS: 1577983-73-3
Formula: C₁₈H₁₆FN₃O
MW: 309.3 g/mol

ZX-005308

Rucaparib Impurity I

CAS: 1408282-26-7
Formula: C₁₁H₉FN₂O
MW: 204.2 g/mol

ZX-005309

Rucaparib Impurity II

CAS: 283173-80-8
Formula: C₁₁H₈BrFN₂O
MW: 283.1 g/mol

ZX-005310

Ruxolitinib 7-Hydroxymethyl Impurity (R- Isomer)

CAS: 1236033-03-6
Formula: C₁₈H₂₀N₆O
MW: 336.4 g/mol

ZX-005311

Ruxolitinib Acrylo Pyrimidine Impurity

CAS: 941685-39-8
Formula: C₂₃H₃₂N₆OSi
MW: 436.6 g/mol

ZX-005312

Ruxolitinib Impurity 11 (Diastereomeric Mixture)

CAS: 1092973-96-0
Formula: C₁₇H₁₆N₆O
MW: 320.3 g/mol

ZX-005313

Ruxolitinib Impurity 3

CAS: 2102675-40-9
Formula: C₁₇H₁₉N₅O₂
MW: 325.4 g/mol

ZX-005314

Ruxolitinib Impurity 6

CAS: 2606144-44-7
Formula: C₁₆H₁₈N₆O₂
MW: 326.35 g/mol

ZX-005315

Ruxolitinib Impurity 7

CAS: 2606144-45-8
Formula: C₁₆H₁₈N₆O
MW: 310.35 g/mol

ZX-005316

Questions

Impurity Reference Standards for Mauritius

Do you ship impurity standards to Mauritius?

Yes. We ship by sea to Port Louis, 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 Mauritius?

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 Pharmacy Board (Ministry of Health and Wellness) is agreed with you at quote stage.

How long does delivery to Mauritius take?

Allow 12–18 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 Mauritius

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

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