Chile · Impurity Reference Standards

Impurity Standards supply to Chile

Zemixal supplies 20,060 products from its impurity reference standards range to buyers in Chile. Locally, the main users are in copper & lithium mining, salmon aquaculture and pulp, paper & forestry. Regular consignments go to industrial centres such as Santiago, Antofagasta and Concepción. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Chile Sample products

20,060products in this division

35–50 dsea transit from India

4–7 dair freight

6categories

Supplying impurity reference standards to Chile

By sea, containers and LCL lots take roughly 35–50 days to San Antonio and Valparaíso. Air cargo to Santiago Arturo Merino Benítez (SCL) takes 4–7 days, which suits small and urgent packs. The relevant authority is ISP (Instituto de Salud Pública). 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 Chile

Authority	ISP (Instituto de Salud Pública)
Seaports	San Antonio, Valparaíso, Antofagasta / Mejillones
Airports	Santiago Arturo Merino Benítez (SCL)
Dangerous goods	IMDG by sea, IATA DGR by air

Medicines and APIs are regulated by the ISP, which grants sanitary registrations and import authorisations. Chile's hazardous substances regulation, DS 57/2019, is phasing in GHS classification, labelling and notification duties for importers. Precursor chemicals must be entered in the special registry for controlled chemical substances. Preferential duty under the India–Chile PTA requires a valid certificate of origin in the agreement's format, and dangerous goods follow IMDG or IATA rules. Your customs broker can confirm which obligations apply to each product.

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.
35–50 daysOcean transit to San Antonio
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: MINSAL / ISP (hazardous substances regulation DS 57/2019).

Indicative total by sea: 42–67 days

By air: about 8–17 days in total.

Documents for Chile

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–Chile PTA format for preferential duty
ISP import authorisation or sanitary registration for pharmaceuticals where required
Controlled chemical substances registry entry for precursors 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 Chile

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

Full impurity reference standards range

4,4-Dimethyloxazolidine-2-thione

CAS: 54013-55-7
Formula: C₅H₉NOS
MW: 131.2 g/mol

ZX-045151

3-Hydroxyphenylacetic Acid

CAS: 621-37-4
Formula: C₈H₈O₃
MW: 152.15 g/mol

ZX-045152

2-Methyl-5-vinylpyridine

CAS: 140-76-1
Formula: C₈H₉N
MW: 119.16 g/mol

ZX-045153

Finafloxacin

CAS: 209342-40-5
Formula: C₂₀H₁₉FN₄O₄
MW: 398.4 g/mol

ZX-045158

Methyl Adipoyl Chloride

CAS: 35444-44-1
Formula: C₇H₁₁ClO₃
MW: 178.61 g/mol

ZX-045159

2,6-Dichloro-4-Cyanopyridine

CAS: 32710-65-9
Formula: C₆H₂Cl₂N₂
MW: 173 g/mol

ZX-045160

Hexanoyl Glycine

CAS: 24003-67-6
Formula: C₈H₁₅NO₃
MW: 173.21 g/mol

ZX-045161

(2-(Methylamino)pyridin-4-yl)methanol

CAS: 193001-42-2
Formula: C₇H₁₀N₂O
MW: 138.17 g/mol

ZX-045166

Methanol-d1

CAS: 1455-13-6
Formula: CH₄O
MW: 33.05 g/mol

ZX-045173

alpha-BHC 13C6

CAS: 222966-66-7
Formula: C₆H₆Cl₆
MW: 296.8 g/mol

ZX-045174

Histrelin

CAS: 76712-82-8
Formula: C₆₆H₈₆N₁₈O₁₂
MW: 1323.5 g/mol

ZX-045175

Benzydamine

CAS: 642-72-8
Formula: C₁₉H₂₃N₃O
MW: 309.4 g/mol

ZX-045176

Questions

Impurity Reference Standards for Chile

Do you ship impurity standards to Chile?

Yes. We ship by sea to San Antonio and Valparaíso, 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 Chile?

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 ISP (Instituto de Salud Pública) is agreed with you at quote stage.

How long does delivery to Chile take?

Allow 35–50 days for ocean transit or 4–7 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 Chile

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

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