Guatemala · Impurity Reference Standards

Impurity Reference Standards shipped to Guatemala

The impurity reference standards division counts 20,060 products, and each one can be quoted for delivery to Guatemala. In Guatemala the strongest demand is from sugar & ethanol, coffee & agro-processing and generic pharmaceuticals. Regular consignments go to industrial centres such as Guatemala City, Escuintla and Villa Nueva. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Guatemala Sample products

20,060products in this division

35–50 dsea transit from India

4–7 dair freight

6categories

Supplying impurity reference standards to Guatemala

By sea, containers and LCL lots take roughly 35–50 days to Puerto Quetzal and Santo Tomás de Castilla. Air cargo to Guatemala City La Aurora (GUA) takes 4–7 days, which suits small and urgent packs. The relevant authority is MSPAS – Department of Regulation and Control of Pharmaceutical Products (DRCPFA). 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 Guatemala

Authority	MSPAS – Department of Regulation and Control of Pharmaceutical Products (DRCPFA)
Seaports	Puerto Quetzal, Santo Tomás de Castilla, Puerto Barrios
Airports	Guatemala City La Aurora (GUA)
Dangerous goods	IMDG by sea, IATA DGR by air

Pharmaceutical products and APIs generally need sanitary registration or import authorisation from MSPAS, through its department for the regulation and control of pharmaceutical products. Importers of precursor and controlled chemicals need prior licensing from the health ministry. Imports clear through SAT customs, with Central American customs harmonisation (SIECA) rules applying. MARN covers environmental aspects of chemical handling. Hazardous cargo must be packed and declared to IMDG or IATA rules. Your local broker can confirm which permits apply to each product before booking.

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 Quetzal
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: MARN (Ministry of Environment and Natural Resources).

Indicative total by sea: 42–67 days

By air: about 8–17 days in total.

Documents for Guatemala

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
MSPAS import permit or sanitary registration for pharmaceutical products where required
Controlled-chemical import licence 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 Guatemala

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

Full impurity reference standards range

Amoxicilin Alpha Penicilloic Acid

CAS: 87860-49-9
Formula: C₁₆H₂₁N₃O₆S
MW: 383.4 g/mol

ZX-023281

Amphotericin B Methyl Ester

CAS: 36148-89-7
Formula: C₄₈H₇₅NO₁₇
MW: 938.1 g/mol

ZX-023282

Amphoteronolide B

CAS: 106799-07-9
Formula: C₄₁H₆₂O₁₄
MW: 778.9 g/mol

ZX-023283

Ampicilloic acid

CAS: 32746-94-4
Formula: C₁₆H₂₁N₃O₅S
MW: 367.4 g/mol

ZX-023284

Ampicillin EP Impurity I

CAS: 10001-82-8
Formula: C₂₄H₂₆N₄O₅S
MW: 482.6 g/mol

ZX-023285

Ampicillin EP Impurity M Disodium Salt

CAS: 94730-51-5
Formula: C₃₂H₃₆N₆Na₂O₈S₂
MW: 742.8 g/mol

ZX-023286

Ampicillin oligomer 1 (trimer)

CAS: 114977-84-3
Formula: C₄₈H₅₇N₉O₁₂S₃
MW: 1048.2 g/mol

ZX-023287

Ampicillin Oligomer 1 (trimer) Sodium Salt

CAS: 94659-48-0
Formula: C₄₈H₅₄N₉Na₃O₁₂S₃
MW: 1114.2 g/mol

ZX-023288

3-(Hydroxymethylene)-6-phenyl-2,5-piperazinedione

CAS: 142975-48-2
Formula: C₁₁H₁₀N₂O₃
MW: 218.21 g/mol

ZX-023289

Amsacrine

CAS: 51264-14-3
Formula: C₂₁H₁₉N₃O₃S
MW: 393.5 g/mol

ZX-023290

Amylmetacresol EP Impurity F

CAS: 150033-77-5
Formula: C₁₂H₁₆O₂
MW: 192.25 g/mol

ZX-023291

Amylmetacresol EP Impurity E

CAS: 173851-66-6
Formula: C₁₂H₁₆O₂
MW: 192.25 g/mol

ZX-023292

Questions

Impurity Reference Standards for Guatemala

Do you ship impurity standards to Guatemala?

Yes. We ship by sea to Puerto Quetzal and Santo Tomás de Castilla, 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 Guatemala?

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 MSPAS – Department of Regulation and Control of Pharmaceutical Products (DRCPFA) is agreed with you at quote stage.

How long does delivery to Guatemala 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 Guatemala

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

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