Zimbabwe · Impurity Reference Standards

Impurity Standards supply to Zimbabwe

Zemixal supplies 20,060 products from its impurity reference standards range to buyers in Zimbabwe. Demand there comes mainly from gold, platinum and lithium mining, tobacco and agro-processing and fertilisers. Regular consignments go to industrial centres such as Harare, Bulawayo and Kwekwe. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Zimbabwe Sample products

20,060products in this division

25–35 dsea transit from India

4–6 dair freight

6categories

Supplying impurity reference standards to Zimbabwe

By sea, containers and LCL lots take roughly 25–35 days to Beira (via road) and Durban (via road). Air cargo to Harare Robert Gabriel Mugabe (HRE) takes 4–6 days, which suits small and urgent packs. The relevant authority is MCAZ (Medicines Control Authority of Zimbabwe). 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 Zimbabwe

Authority	MCAZ (Medicines Control Authority of Zimbabwe)
Seaports	Beira (via road), Durban (via road)
Airports	Harare Robert Gabriel Mugabe (HRE)
Dangerous goods	IMDG by sea, IATA DGR by air

The Environmental Management Agency (EMA) licenses imports of hazardous substances, and MCAZ registers medicines and issues import permits for APIs. Certain regulated product categories also need a Consignment Based Conformity Assessment (CBCA) certificate before shipment, so check the HS code early. Cargo usually arrives via Beira or Durban under transit documents. Transactions are commonly settled in US dollars. Dangerous goods follow IMDG rules at sea and regional road transport rules on the inland leg.

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 Beira (via road)
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: EMA (Environmental Management Agency).

Indicative total by sea: 32–52 days

By air: about 8–16 days in total.

Documents for Zimbabwe

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
EMA hazardous substances import licence where applicable
MCAZ import permit for APIs and medicines
CBCA certificate where the product category requires it
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 Zimbabwe

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

Full impurity reference standards range

Noradrenalone EP Impurity B (Hydrochloride Salt)

CAS: 5090-29-9
Formula: C₈H₁₀ClNO₃
MW: 203.62 g/mol

ZX-005857

Norethisterone EP Impurity B

CAS: 734-32-7
Formula: C₁₈H₂₄O₂
MW: 272.4 g/mol

ZX-005858

Ofloxacin EP Impurity A

CAS: 82419-35-0
Formula: C₁₃H₉F₂NO₄
MW: 281.21 g/mol

ZX-005859

Ofloxacin EP Impurity C

CAS: 95848-94-5
Formula: C₁₈H₂₁N₃O₄
MW: 343.4 g/mol

ZX-005860

Olanzapine EP Impurity A

CAS: 138564-59-7
Formula: C₁₂H₉N₃O₂S
MW: 259.29 g/mol

ZX-005861

Olanzapine EP Impurity B

CAS: 221176-49-4
Formula: C₁₂H₁₀N₂OS
MW: 230.29 g/mol

ZX-005862

Olanzapine EP Impurity C

CAS: 719300-59-1
Formula: C₁₈H₂₂Cl₂N₄S
MW: 397.4 g/mol

ZX-005863

Olmesartan EP Impurity A

CAS: 144689-24-7
Formula: C₂₄H₂₆N₆O₃
MW: 446.5 g/mol

ZX-005864

Omeprazole EP impurity F & G Mixture

CAS: 125656-82-8
Formula: C₁₆H₁₃N₃O₂S
MW: 311.4 g/mol

ZX-005865

Omeprazole EP Impurity G

CAS: 125656-83-9
Formula: C₁₆H₁₃N₃O₂S
MW: 311.4 g/mol

ZX-005866

Omeprazole EP Impurity XI

CAS: 86604-75-3
Formula: C₉H₁₃Cl₂NO
MW: 222.11 g/mol

ZX-005867

Oxcarbazepine EP Impurity M

CAS: 2642430-32-6
Formula: C₃₀H₂₂N₄O₃
MW: 486.5 g/mol

ZX-005868

Questions

Impurity Reference Standards for Zimbabwe

Do you ship impurity standards to Zimbabwe?

Yes. We ship by sea to Beira (via road) and Durban (via road), 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 Zimbabwe?

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 MCAZ (Medicines Control Authority of Zimbabwe) is agreed with you at quote stage.

How long does delivery to Zimbabwe take?

Allow 25–35 days for ocean transit or 4–6 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 Zimbabwe

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

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