Ghana · Impurity Reference Standards

Impurity Standards supply to Ghana

The impurity reference standards division counts 20,060 products, and each one can be quoted for delivery to Ghana. Locally, the main users are in pharmaceutical manufacturing, gold mining and cocoa processing. Regular consignments go to industrial centres such as Tema, Accra and Kumasi. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Ghana Sample products

20,060products in this division

25–35 dsea transit from India

3–6 dair freight

6categories

Supplying impurity reference standards to Ghana

By sea, containers and LCL lots take roughly 25–35 days to Tema and Takoradi. Air cargo to Accra Kotoka (ACC) takes 3–6 days, which suits small and urgent packs. The relevant authority is FDA Ghana (Food and Drugs Authority). 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 Ghana

Authority	FDA Ghana (Food and Drugs Authority)
Seaports	Tema, Takoradi
Airports	Accra Kotoka (ACC)
Dangerous goods	IMDG by sea, IATA DGR by air

Industrial and hazardous chemicals generally need registration or an import permit from Ghana's Environmental Protection Authority. APIs and pharmaceutical raw materials require an FDA Ghana import permit, which the importer should obtain before shipment. Customs declarations are processed through the national single window, so the consignee, HS codes and values on our invoice must match the declaration. Mining reagents are often hazardous, and shipments carrying them must have an IMDG or IATA dangerous goods declaration. There is no India–Ghana trade agreement in force.

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 Tema
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: EPA Ghana (Environmental Protection Authority).

Indicative total by sea: 32–52 days

By air: about 7–16 days in total.

Documents for Ghana

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
EPA Ghana chemical import permit where applicable
FDA Ghana import permit for APIs 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 Ghana

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

Full impurity reference standards range

(S)-4-Benzyl-2-oxazolidinone

CAS: 90719-32-7
Formula: C₁₀H₁₁NO₂
MW: 177.2 g/mol

ZX-022803

PAPE-Ethyl carbamate

CAS: 2206827-12-3
Formula: C₁₆H₁₇N₃O₄
MW: 315.32 g/mol

ZX-022804

Sotalol Hydrochloride

CAS: 959-24-0
Formula: C₁₂H₂₁ClN₂O₃S
MW: 308.83 g/mol

ZX-022805

Deshydroxy Sotalol Hydrochloride

CAS: 16974-44-0
Formula: C₁₂H₂₁ClN₂O₂S
MW: 292.83 g/mol

ZX-022806

Oxo Sotalol Hydrochloride

CAS: 5576-49-8
Formula: C₁₂H₁₉ClN₂O₃S
MW: 306.81 g/mol

ZX-022807

4-((S)-4-Acryloyl-2-methylpiperazin-1-yl)-6-fluoro-7-(2-fluoro-6-hydroxyphenyl)-1-(2-isopropyl-4-methylpyridin-3-yl)pyrido[2,3-d]pyrimidin-2(1H)-one

CAS: 2252403-56-6
Formula: C₃₀H₃₀F₂N₆O₃
MW: 560.6 g/mol

ZX-022808

Sotorasib

CAS: 2296729-00-3
Formula: C₃₀H₃₀F₂N₆O₃
MW: 560.6 g/mol

ZX-022809

Stavudine

CAS: 3056-17-5
Formula: C₁₀H₁₂N₂O₄
MW: 224.21 g/mol

ZX-022810

1-(Benzo[d][1,3]dioxol-5-yl)-4,4-dimethylpentan-3-ol

CAS: 106175-03-5
Formula: C₁₄H₂₀O₃
MW: 236.31 g/mol

ZX-022811

Sucralose EP Impurity B

CAS: 40631-75-2
Formula: C₁₂H₁₉Cl₃O₈
MW: 397.6 g/mol

ZX-022812

Sucralose EP Impurity H

CAS: 78508-21-1
Formula: C₆H₁₀Cl₂O₄
MW: 217.04 g/mol

ZX-022813

Sucralose EP Impurity I

CAS: 848642-13-7
Formula: C₆H₁₁ClO₅
MW: 198.6 g/mol

ZX-022814

Questions

Impurity Reference Standards for Ghana

Do you ship impurity standards to Ghana?

Yes. We ship by sea to Tema and Takoradi, 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 Ghana?

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 FDA Ghana (Food and Drugs Authority) is agreed with you at quote stage.

How long does delivery to Ghana take?

Allow 25–35 days for ocean transit or 3–6 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 Ghana

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

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