Morocco · Impurity Reference Standards

Impurity Reference Standards for Morocco

Buyers in Morocco can order any of the 20,060 products in our impurity reference standards division. Locally, the main users are in phosphates & fertilisers, pharmaceutical manufacturing and automotive. Typical delivery points include Casablanca, Jorf Lasfar and Safi. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Morocco Sample products

20,060products in this division

18–26 dsea transit from India

3–6 dair freight

6categories

Supplying impurity reference standards to Morocco

Sea freight reaches Casablanca and Tanger Med in about 18–26 days port to port. Urgent or small lots fly to Casablanca Mohammed V (CMN) in 3–6 days. Import compliance for this category sits with AMMPS (Moroccan Medicines & Health Products Agency), Ministry of Health, 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 Morocco

Authority	AMMPS (Moroccan Medicines & Health Products Agency), Ministry of Health
Seaports	Casablanca, Tanger Med, Jorf Lasfar
Airports	Casablanca Mohammed V (CMN)
Dangerous goods	IMDG by sea, IATA DGR by air

Imports are declared electronically through the PortNet single window, where the importer files the import commitment before shipment. Hazardous chemicals may need prior authorisation from the relevant ministry depending on the substance and its end use. APIs are supervised by AMMPS, the Moroccan medicines and health products agency, which generally expects GMP-compliant sources and registered finished products. French-language documentation is common, so confirm what your broker needs. Dangerous goods must be packed and declared under IMDG or IATA rules. India and Morocco have no 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.
18–26 daysOcean transit to Casablanca
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 Energy Transition & Sustainable Development / Ministry of Industry.

Indicative total by sea: 25–43 days

By air: about 7–16 days in total.

Documents for Morocco

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
Import commitment/declaration via PortNet
Prior authorisation for regulated chemicals where applicable
AMMPS 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 Morocco

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

Full impurity reference standards range

(11β)-11,20-Dihydroxy-3-oxo-pregna-1,4-dien-21-oic acid (Mixture of ismoers)

CAS: 75448-52-1
Formula: C₂₁H₂₈O₅
MW: 360.4 g/mol

ZX-031969

Prednisolone E-enol aldehyde impurity

CAS: 118864-88-3
Formula: C₂₁H₂₆O₄
MW: 342.4 g/mol

ZX-031970

3,20-Disemicarbazone-17,21-dihydroxy-pregna-1,4-diene-3,11,20-trione 21-Acetate

CAS: 115097-56-8
Formula: C₂₅H₃₄N₆O₆
MW: 514.6 g/mol

ZX-031971

Prednisone EP Impurity C

CAS: 70522-55-3
Formula: C₂₁H₂₄O₅
MW: 356.4 g/mol

ZX-031972

Pregabalin 3-Cyano Impurity

CAS: 181289-16-7
Formula: C₈H₁₃NO₂
MW: 155.19 g/mol

ZX-031973

4-Isobutylpiperidine-2,6-dione

CAS: 916982-10-0
Formula: C₉H₁₅NO₂
MW: 169.22 g/mol

ZX-031974

4,9-Diisobutyl-1,6-diazecane-2,7-dione

CAS: 1990538-03-8
Formula: C₁₆H₃₀N₂O₂
MW: 282.42 g/mol

ZX-031975

Pregabalin Methyl Ester Hydrochloride

CAS: 714230-22-5
Formula: C₉H₂₀ClNO₂
MW: 209.71 g/mol

ZX-031976

Pregabalin N-Methyl Impurity

CAS: 1155843-61-0
Formula: C₉H₁₉NO₂
MW: 173.25 g/mol

ZX-031977

(3S)-3-(2-Amino-2-oxoethyl)-5-methylhexanoic Acid

CAS: 181289-34-9
Formula: C₉H₁₇NO₃
MW: 187.24 g/mol

ZX-031978

3-Isobutylglutaric Anhydride

CAS: 185815-59-2
Formula: C₉H₁₄O₃
MW: 170.21 g/mol

ZX-031979

Pregabalin conjugate PD0224378

CAS: 466678-44-4
Formula: C₂₀H₃₅NO₁₁
MW: 465.5 g/mol

ZX-031980

Questions

Impurity Reference Standards for Morocco

Can Zemixal deliver impurity reference standards to Morocco?

Yes. We ship by sea to Casablanca and Tanger Med, 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 Morocco?

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 AMMPS (Moroccan Medicines & Health Products Agency), Ministry of Health is agreed with you at quote stage.

How long does delivery to Morocco take?

Allow 18–26 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 Morocco

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

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