Honduras · Impurity Reference Standards

Impurity Reference Standards for Honduras

The impurity reference standards division counts 20,060 products, and each one can be quoted for delivery to Honduras. Demand there comes mainly from textiles & apparel (maquila), coffee & palm oil processing and shrimp aquaculture. Typical delivery points include San Pedro Sula, Tegucigalpa and Choloma. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Honduras Sample products

20,060products in this division

35–50 dsea transit from India

4–7 dair freight

6categories

Supplying impurity reference standards to Honduras

Sea freight reaches Puerto Cortés and San Lorenzo in about 35–50 days port to port. Urgent or small lots fly to San Pedro Sula (SAP) in 4–7 days. Import compliance for this category sits with ARSA (Agencia de Regulación Sanitaria), 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 Honduras

Authority	ARSA (Agencia de Regulación Sanitaria)
Seaports	Puerto Cortés, San Lorenzo
Airports	San Pedro Sula (SAP), Palmerola (XPL)
Dangerous goods	IMDG by sea, IATA DGR by air

Medicines, APIs and many health-related products need sanitary registration or an import authorisation from ARSA, the health regulation agency, before customs release. Precursor and controlled chemicals require additional licensing held by the importer. Environmental matters fall under MiAmbiente. Dangerous goods must be packed, labelled and declared under IMDG or IATA rules, and clearance follows Central American (SIECA) customs procedures. Importers should confirm whether each product needs ARSA approval before ordering, because goods without it can be held at the port. Your customs broker can check this early.

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 Puerto Cortés
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: SERNA / MiAmbiente (Secretariat of Natural Resources and Environment).

Indicative total by sea: 42–67 days

By air: about 8–17 days in total.

Documents for Honduras

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
ARSA sanitary registration or import authorisation where required
Controlled-chemical import permit 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 Honduras

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

Full impurity reference standards range

Dehydrocholic Acid

CAS: 81-23-2
Formula: C₂₄H₃₄O₅
MW: 402.5 g/mol

ZX-022396

N-Nitroso-2-Pyrrolidinone

CAS: 54634-49-0
Formula: C₄H₆N₂O₂
MW: 114.1 g/mol

ZX-022397

Hexetidine EP Impurity C

CAS: 5980-31-4
Formula: C₂₂H₄₅N₃
MW: 351.6 g/mol

ZX-022398

3,6-Difluoropyrazine-2-carbonitrile

CAS: 356783-28-3
Formula: C₅HF₂N₃
MW: 141.08 g/mol

ZX-022399

6-Aminoisoquinoline

CAS: 23687-26-5
Formula: C₉H₈N₂
MW: 144.17 g/mol

ZX-022400

2,4-Dimethylbenzoic acid

CAS: 611-01-8
Formula: C₉H₁₀O₂
MW: 150.17 g/mol

ZX-022401

Aclonifen

CAS: 74070-46-5
Formula: C₁₂H₉ClN₂O₃
MW: 264.66 g/mol

ZX-022402

2-Naphthalenecarboxylic Acid

CAS: 93-09-4
Formula: C₁₁H₈O₂
MW: 172.18 g/mol

ZX-022403

2-Hydroxy-3-methoxy-3,3-diphenylpropanoic Acid

CAS: 178306-51-9
Formula: C₁₆H₁₆O₄
MW: 272.29 g/mol

ZX-022404

Cyclo(-Ala-Gln)

CAS: 268221-76-7
Formula: C₈H₁₃N₃O₃
MW: 199.21 g/mol

ZX-022405

Benzyl Tosylate

CAS: 1024-41-5
Formula: C₁₄H₁₄O₃S
MW: 262.33 g/mol

ZX-022406

3-Hydroxy-4-Methoxy Benzonitrile

CAS: 52805-46-6
Formula: C₈H₇NO₂
MW: 149.15 g/mol

ZX-022407

Questions

Impurity Reference Standards for Honduras

Can Zemixal deliver impurity reference standards to Honduras?

Yes. We ship by sea to Puerto Cortés and San Lorenzo, 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 Honduras?

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 ARSA (Agencia de Regulación Sanitaria) is agreed with you at quote stage.

How long does delivery to Honduras 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 Honduras

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

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