Brazil · Impurity Reference Standards

Impurity Standards supply to Brazil

The impurity reference standards division counts 20,060 products, and each one can be quoted for delivery to Brazil. Locally, the main users are in generic pharmaceuticals, agrochemicals & crop protection and petrochemicals & plastics. Typical delivery points include São Paulo & Campinas, Camaçari (Bahia) and Rio de Janeiro. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Brazil Sample products

20,060products in this division

30–45 dsea transit from India

4–6 dair freight

6categories

Supplying impurity reference standards to Brazil

Sea freight reaches Santos and Paranaguá in about 30–45 days port to port. Urgent or small lots fly to São Paulo Guarulhos (GRU) in 4–6 days. Import compliance for this category sits with ANVISA, 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 Brazil

Authority	ANVISA
Seaports	Santos, Paranaguá, Itajaí / Navegantes
Airports	São Paulo Guarulhos (GRU), Campinas Viracopos (VCP)
Dangerous goods	IMDG by sea, IATA DGR by air

Many chemical imports need an LI or LPCO licence through the Siscomex Portal Único before shipment, so ask your despachante to check the NCM code early. APIs require an ANVISA-authorised importer, and many must be linked to a product registration or a CADIFA assessment before use in registered medicines. Drug precursors need Polícia Federal licensing and prior import authorisation, and some substances are also controlled by the Army. Law 15.022/2024 is introducing a national industrial chemicals inventory, with obligations phased in by regulation. Dangerous goods follow IMDG or IATA rules. Request the PTA certificate of origin for preferential duty.

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.
30–45 daysOcean transit to Santos
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: Ibama / CONAMA. Polícia Federal (controlled chemicals). Law 15.022/2024 industrial chemicals inventory.

Indicative total by sea: 37–62 days

By air: about 8–16 days in total.

Documents for Brazil

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
Certificate of Origin in India–MERCOSUR PTA format for preferential duty
Import licence (LI/LPCO) via Siscomex Portal Único where required
ANVISA import authorisation and API registration or CADIFA reference where applicable
Polícia Federal prior import authorisation for controlled chemicals 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 Brazil

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

Full impurity reference standards range

5-Ethyl-2-methylpyridine

CAS: 104-90-5
Formula: C₈H₁₁N
MW: 121.18 g/mol

ZX-018634

3-Methylcholanthrene

CAS: 56-49-5
Formula: C₂₁H₁₆
MW: 268.4 g/mol

ZX-018642

Isopropanol-D8

CAS: 22739-76-0
Formula: C₃H₈O
MW: 68.14 g/mol

ZX-018653

Fosfructose Trisodium Octahydrate

CAS: 81028-91-3
Formula: C₆H₂₇Na₃O₂₀P₂
MW: 550.18 g/mol

ZX-018659

Dichlorophen

CAS: 97-23-4
Formula: C₁₃H₁₀Cl₂O₂
MW: 269.12 g/mol

ZX-018676

N-(Hydroxymethyl)phthalimide

CAS: 118-29-6
Formula: C₉H₇NO₃
MW: 177.16 g/mol

ZX-018679

Ionomycin Calcium

CAS: 56092-82-1
Formula: C₄₁H₇₀CaO₉
MW: 747.1 g/mol

ZX-018740

4-Methylumbelliferyl beta-D-glucuronide

CAS: 6160-80-1
Formula: C₁₆H₁₆O₉
MW: 352.29 g/mol

ZX-018756

Uridine-5'-triphosphate Trisodium Salt Dihydrate

CAS: 116295-90-0
Formula: C₉H₁₆N₂Na₃O₁₇P₃
MW: 586.12 g/mol

ZX-018760

Ferrous Gluconate Hydrate

CAS: 699014-53-4
Formula: C₁₂H₂₆FeO₁₅
MW: 466.17 g/mol

ZX-018824

Chlorophyllin Copper Trisodium Salt

CAS: 11006-34-1
Formula: C₃₄H₃₁CuN₄Na₃O₆
MW: 724.1 g/mol

ZX-018874

(-)-Norephedrine

CAS: 492-41-1
Formula: C₉H₁₃NO
MW: 151.21 g/mol

ZX-018894

Questions

Impurity Reference Standards for Brazil

Can Zemixal deliver impurity reference standards to Brazil?

Yes. We ship by sea to Santos and Paranaguá, 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 Brazil?

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 ANVISA is agreed with you at quote stage.

How long does delivery to Brazil take?

Allow 30–45 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 Brazil

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

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