Tunisia · Impurity Reference Standards

Impurity Reference Standards for Tunisia

Zemixal supplies 20,060 products from its impurity reference standards range to buyers in Tunisia. Locally, the main users are in phosphates & fertilisers, pharmaceutical manufacturing and textiles. Regular consignments go to industrial centres such as Gabès, Sfax and Tunis. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Tunisia Sample products

20,060products in this division

20–30 dsea transit from India

4–6 dair freight

6categories

Supplying impurity reference standards to Tunisia

By sea, containers and LCL lots take roughly 20–30 days to Radès and Sfax. Air cargo to Tunis–Carthage (TUN) takes 4–6 days, which suits small and urgent packs. The relevant authority is DPM (Direction de la Pharmacie et du Médicament), Ministry of Health. 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 Tunisia

Authority	DPM (Direction de la Pharmacie et du Médicament), Ministry of Health
Seaports	Radès, Sfax, Bizerte
Airports	Tunis–Carthage (TUN)
Dangerous goods	IMDG by sea, IATA DGR by air

Imports are processed through the TradeNet single window, and hazardous or controlled chemicals may need technical approval from the relevant ministry before customs releases them. APIs are supervised by the Direction de la Pharmacie et du Médicament at the Ministry of Health, and some pharmaceutical imports are channelled through the state Pharmacie Centrale, so check which route applies to your order. French documentation is standard. Dangerous goods follow IMDG or IATA rules. There is no India–Tunisia 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.
20–30 daysOcean transit to Radès
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 / ANPE.

Indicative total by sea: 27–47 days

By air: about 8–16 days in total.

Documents for Tunisia

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
Technical import approval for regulated chemicals where applicable
Ministry of Health approval 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 Tunisia

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

Full impurity reference standards range

Verapamil EP Impurity F (HCl)

CAS: 67775-97-7
Formula: C₁₇H₂₇ClN₂O₂
MW: 326.9 g/mol

ZX-023010

Vibegron

CAS: 1190389-15-1
Formula: C₂₆H₂₈N₄O₃
MW: 444.5 g/mol

ZX-023011

(αR,2R)-3,4-Dihydro-5-[(4-nitrophenyl)methyl]-α-phenyl-2H-pyrrole-2-methanol

CAS: 1628836-09-8
Formula: C₁₈H₁₈N₂O₃
MW: 310.3 g/mol

ZX-023012

(R)-((2R,5R)-5-(4-Aminobenzyl)pyrrolidin-2-yl)(phenyl)methanol

CAS: 1426235-11-1
Formula: C₁₈H₂₂N₂O
MW: 282.4 g/mol

ZX-023013

tert-Butyl (4R,5R)-4-(Hydroxymethyl)-2,2-dimethyl-5-phenyl-1,3-oxazolidine-3-carboxylate

CAS: 1009092-91-4
Formula: C₁₇H₂₅NO₄
MW: 307.4 g/mol

ZX-023014

Vigabatrin EP Impurity C

CAS: 71107-19-2
Formula: C₇H₁₀N₂O₂
MW: 154.17 g/mol

ZX-023015

Vigabatrin EP Impurity F

CAS: 794466-81-2
Formula: C₁₂H₂₀N₂O₃
MW: 240.3 g/mol

ZX-023016

(E)-2-(2-Aminoethyl)but-2-enoic Acid Hydrochloride

CAS: 1379403-11-8
Formula: C₆H₁₂ClNO₂
MW: 165.62 g/mol

ZX-023017

4-Oxo-6-(2-oxo-5-vinylpyrrolidin-1-yl)hexanoic Acid

CAS: 2512190-67-7
Formula: C₁₂H₁₇NO₄
MW: 239.27 g/mol

ZX-023018

Vilanterol Dimer

CAS: 2762285-55-0
Formula: C₄₈H₆₄Cl₄N₂O₉
MW: 954.8 g/mol

ZX-023019

6-(2-((2,6-Dichlorobenzyl)oxy)ethoxy)hexan-1-amine

CAS: 1463889-71-5
Formula: C₁₅H₂₃Cl₂NO₂
MW: 320.3 g/mol

ZX-023020

(S)-Vilanterol

CAS: 2514963-34-7
Formula: C₂₄H₃₃Cl₂NO₅
MW: 486.4 g/mol

ZX-023021

Questions

Impurity Reference Standards for Tunisia

Do you ship impurity standards to Tunisia?

Yes. We ship by sea to Radès and Sfax, 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 Tunisia?

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 DPM (Direction de la Pharmacie et du Médicament), Ministry of Health is agreed with you at quote stage.

How long does delivery to Tunisia take?

Allow 20–30 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 Tunisia

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

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