Italy · Impurity Reference Standards

Impurity Reference Standards for Italy

Buyers in Italy can order any of the 20,060 products in our impurity reference standards division. In Italy the strongest demand is from pharmaceuticals & generics, fine chemicals & APIs and cosmetics. Regular consignments go to industrial centres such as Milan – Lombardy, Latina (Lazio) and Tuscany (Florence / Siena). Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Italy Sample products

20,060products in this division

16–22 dsea transit from India

3–5 dair freight

6categories

Supplying impurity reference standards to Italy

By sea, containers and LCL lots take roughly 16–22 days to Genoa and La Spezia. Air cargo to Milan Malpensa (MXP) takes 3–5 days, which suits small and urgent packs. The relevant authority is AIFA / 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 Italy

Authority	AIFA / EMA
Seaports	Genoa, La Spezia, Trieste
Airports	Milan Malpensa (MXP), Rome Fiumicino (FCO)
Dangerous goods	IMDG by sea, IATA DGR by air

Italy applies EU REACH and CLP. Where a substance is imported at 1 tonne or more per year, the EU importer or an Only Representative for the Indian manufacturer must register it. SDS and labels must be in Italian. Medicinal active substances need GMP compliance and an EU written confirmation, with AIFA supervising authorised importers. Dangerous goods are packed and declared to 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.
16–22 daysOcean transit to Genoa
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: 23–39 days

By air: about 7–15 days in total.

Documents for Italy

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 Italy

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

Full impurity reference standards range

1-Bromo-9-(tert-butyldimethylsilyloxy)nonane

CAS: 149051-24-1
Formula: C₁₅H₃₃BrOSi
MW: 337.41 g/mol

ZX-029656

9-[[9-[(4,4,5,5,5-Pentafluoropentyl)sulfenyl]nonyl]sulfenyl]nonyl Bromide

CAS: 1391053-14-7
Formula: C₂₃H₄₂BrF₅S₂
MW: 557.6 g/mol

ZX-029657

9-Hydroxynonyl carbamimidothioate

CAS: 741246-55-9
Formula: C₁₀H₂₂N₂OS
MW: 218.36 g/mol

ZX-029658

Fulvestrant R enantiomer

CAS: 1807900-80-6
Formula: C₃₂H₄₇F₅O₃S
MW: 606.8 g/mol

ZX-029659

Fulvestrant S enantiomer

CAS: 1316849-17-8
Formula: C₃₂H₄₇F₅O₃S
MW: 606.8 g/mol

ZX-029660

Fulvestrant Side Chain Impurity

CAS: 148757-89-5
Formula: C₁₄H₂₄BrF₅S
MW: 399.3 g/mol

ZX-029661

Furagin

CAS: 1672-88-4
Formula: C₁₀H₈N₄O₅
MW: 264.19 g/mol

ZX-029662

Furosemide Amide Impurity

CAS: 4793-47-9
Formula: C₁₂H₁₂ClN₃O₄S
MW: 329.76 g/mol

ZX-029664

N-Nitroso-Furosemide

CAS: 2708280-93-5
Formula: C₁₂H₁₀ClN₃O₆S
MW: 359.74 g/mol

ZX-029665

Furosemide-d5

CAS: 1189482-35-6
Formula: C₁₂H₁₁ClN₂O₅S
MW: 335.78 g/mol

ZX-029666

Diethanolamine Fusidate

CAS: 16391-75-6
Formula: C₃₅H₅₉NO₈
MW: 621.8 g/mol

ZX-029667

Sodium Fusidate

CAS: 751-94-0
Formula: C₃₁H₄₇NaO₆
MW: 538.7 g/mol

ZX-029668

Questions

Impurity Reference Standards for Italy

Do you ship impurity standards to Italy?

Yes. We ship by sea to Genoa and La Spezia, 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 Italy?

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 AIFA / EMA is agreed with you at quote stage.

How long does delivery to Italy take?

Allow 16–22 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 Italy

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

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