Austria · Impurity Reference Standards

Impurity Standards supply to Austria

Zemixal supplies 20,060 products from its impurity reference standards range to buyers in Austria. Demand there comes mainly from antibiotics & biosimilars, steel & metallurgy and plastics & fibres. Regular consignments go to industrial centres such as Linz, Vienna and Kundl / Schaftenau (Tyrol). Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Austria Sample products

20,060products in this division

20–28 dsea transit from India

3–5 dair freight

6categories

Supplying impurity reference standards to Austria

By sea, containers and LCL lots take roughly 20–28 days to Koper (via rail) and Trieste (via rail). Air cargo to Vienna (VIE) takes 3–5 days, which suits small and urgent packs. The relevant authority is BASG (AGES) / 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 Austria

Authority	BASG (AGES) / EMA
Seaports	Koper (via rail), Trieste (via rail), Hamburg (via rail)
Airports	Vienna (VIE), Linz (LNZ)
Dangerous goods	IMDG by sea, IATA DGR by air

Austria follows EU REACH and CLP. For any substance arriving at 1 tonne or more per year, registration sits with the EU importer or with an Only Representative acting for the non-EU manufacturer. Labels and the SDS must be in German. If you import an active substance for a medicinal product, the Indian manufacturer needs GMP compliance and an EU written confirmation, and BASG oversees authorised importers. Dangerous goods are packed and declared to IMDG or IATA rules, and customs clearance needs 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.
20–28 daysOcean transit to Koper (via rail)
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: 27–45 days

By air: about 7–15 days in total.

Documents for Austria

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 Austria

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

Full impurity reference standards range

Colchicine EP Impurity D

CAS: 477-29-2
Formula: C₂₇H₃₃NO₁₁
MW: 547.5 g/mol

ZX-021178

Chlormadinone

CAS: 1961-77-9
Formula: C₂₁H₂₇ClO₃
MW: 362.9 g/mol

ZX-021179

Amiloride EP Impurity B

CAS: 4878-36-8
Formula: C₅H₅ClN₄O₂
MW: 188.57 g/mol

ZX-021180

Hydrochlorothiazide EP Impurity A

CAS: 58-94-6
Formula: C₇H₆ClN₃O₄S₂
MW: 295.7 g/mol

ZX-021181

Desmethyl Chlorpheniramine Maleate Salt

CAS: 22630-25-7
Formula: C₁₉H₂₁ClN₂O₄
MW: 376.8 g/mol

ZX-021182

Chlorphenamine EP Impurity D

CAS: 65676-21-3
Formula: C₁₇H₁₈ClN₃
MW: 299.8 g/mol

ZX-021183

Chlorphenamine EP Impurity A

CAS: 1246816-57-8
Formula: C₁₆H₂₄ClN₃
MW: 293.83 g/mol

ZX-021184

Chlorpheniramine N-Oxide

CAS: 120244-82-8
Formula: C₁₆H₁₉ClN₂O
MW: 290.79 g/mol

ZX-021185

R-Chlorpheniramine Maleate

CAS: 23095-76-3
Formula: C₂₀H₂₃ClN₂O₄
MW: 390.9 g/mol

ZX-021186

Pheniramine

CAS: 86-21-5
Formula: C₁₆H₂₀N₂
MW: 240.34 g/mol

ZX-021187

Chlorpromazine Hydrochloride

CAS: 69-09-0
Formula: C₁₇H₂₀Cl₂N₂S
MW: 355.3 g/mol

ZX-021188

Chlorpromazine EP Impurity A

CAS: 969-99-3
Formula: C₁₇H₁₉ClN₂OS
MW: 334.9 g/mol

ZX-021189

Questions

Impurity Reference Standards for Austria

Do you ship impurity standards to Austria?

Yes. We ship by sea to Koper (via rail) and Trieste (via rail), 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 Austria?

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 BASG (AGES) / EMA is agreed with you at quote stage.

How long does delivery to Austria take?

Allow 20–28 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 Austria

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

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