France · Impurity Reference Standards

Impurity Reference Standards shipped to France

Zemixal supplies 20,060 products from its impurity reference standards range to buyers in France. Locally, the main users are in pharmaceuticals & vaccines, cosmetics & fragrances and petrochemicals & polymers. Regular consignments go to industrial centres such as Lyon (Vallée de la Chimie), Rouen – Le Havre (Seine axis) and Fos-Berre (Marseille). Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

France Sample products

20,060products in this division

18–27 dsea transit from India

3–5 dair freight

6categories

Supplying impurity reference standards to France

By sea, containers and LCL lots take roughly 18–27 days to Le Havre and Marseille-Fos. Air cargo to Paris Charles de Gaulle (CDG) takes 3–5 days, which suits small and urgent packs. The relevant authority is ANSM / EMA. 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 France

Authority	ANSM / EMA
Seaports	Le Havre, Marseille-Fos, Dunkirk
Airports	Paris Charles de Gaulle (CDG), Lyon (LYS)
Dangerous goods	IMDG by sea, IATA DGR by air

France applies EU REACH and CLP, so any substance imported at 1 tonne or more per year needs registration by the EU importer or by an Only Representative for the Indian manufacturer. SDS and labels must be in French. Active substances destined for medicines need GMP compliance and an EU written confirmation, and ANSM supervises authorised importers. Dangerous goods are packed and declared under IMDG or IATA DGR, and customs clearance requires the importer's EORI number.

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.
18–27 daysOcean transit to Le Havre
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: ECHA (EU REACH & CLP).

Indicative total by sea: 25–44 days

By air: about 7–15 days in total.

Documents for France

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
REACH registration number or OR declaration (substances ≥1 t/yr)
EU Written Confirmation for API imports (Art. 46b Directive 2001/83/EC)
Dangerous Goods Declaration (IMDG/IATA) where applicable
Importer's EORI number

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 France

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

Full impurity reference standards range

Descarbamoyl Degarelix Impurity

CAS: 2648486-37-5
Formula: C₈₁H₁₀₂ClN₁₇O₁₅
MW: 1589.2 g/mol

ZX-024203

Delafloxacin

CAS: 189279-58-1
Formula: C₁₈H₁₂ClF₃N₄O₄
MW: 440.8 g/mol

ZX-024204

Deschloro-delafloxacin

CAS: 959374-64-2
Formula: C₁₈H₁₃F₃N₄O₄
MW: 406.3 g/mol

ZX-024205

Delafloxacin Dimer Impurity

CAS: 1093185-35-3
Formula: C₃₆H₂₄Cl₂F₆N₈O₈
MW: 881.5 g/mol

ZX-024206

3-Descarboxy 3-Hydroxy Delafloxacin

CAS: 2097714-10-6
Formula: C₁₇H₁₂ClF₃N₄O₃
MW: 412.7 g/mol

ZX-024207

4-[4-(Trifluoromethoxy)phenoxy]piperidine

CAS: 287952-67-4
Formula: C₁₂H₁₄F₃NO₂
MW: 261.24 g/mol

ZX-024208

(R)-2-Methyl-3-(4-(4-(4-(trifluoromethoxy)phenoxy)piperidin-1-yl)phenoxy)propane-1,2-diol

CAS: 1318735-00-0
Formula: C₂₂H₂₆F₃NO₅
MW: 441.4 g/mol

ZX-024209

Deltamethric Acid Chloride

CAS: 55710-82-2
Formula: C₈H₉Br₂ClO
MW: 316.42 g/mol

ZX-024210

Demeclocycline Hydrochloride

CAS: 64-73-3
Formula: C₂₁H₂₂Cl₂N₂O₈
MW: 501.3 g/mol

ZX-024211

Demeclocycline EP Impurity B

CAS: 14206-59-8
Formula: C₂₁H₂₁ClN₂O₈
MW: 464.9 g/mol

ZX-024212

Demeclocycline EP Impurity C

CAS: 129044-45-7
Formula: C₂₁H₂₂N₂O₈
MW: 430.4 g/mol

ZX-024213

Demeclocycline EP Impurity F

CAS: 81181-91-1
Formula: C₂₁H₁₉ClN₂O₇
MW: 446.8 g/mol

ZX-024214

Questions

Impurity Reference Standards for France

Do you ship impurity standards to France?

Yes. We ship by sea to Le Havre and Marseille-Fos, 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 France?

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 ANSM / EMA is agreed with you at quote stage.

How long does delivery to France take?

Allow 18–27 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 France

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

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