Guatemala · Pharmaceutical Intermediates

Pharmaceutical Intermediates shipped to Guatemala

Zemixal supplies 14,468 products from its pharmaceutical intermediates range to buyers in Guatemala. Demand there comes mainly 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 API manufacturers, CDMOs and CMOs and medicinal and discovery chemistry groups.

Guatemala Sample products

14,468products in this division

35–50 dsea transit from India

4–7 dair freight

4categories

Supplying pharmaceutical intermediates 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 Key starting material (KSM) specification, Advanced intermediate (customer spec), Building block, ≥95% / ≥98% purity and Chiral (ee specified).

Grades in this division

Key starting material (KSM) specificationAdvanced intermediate (customer spec)Building block, ≥95% / ≥98% purityChiral (ee specified)Technical gradeLow genotoxic-impurity specification

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 pharmaceutical intermediates

Organic Building Blocks 8,529Heterocyclic Building Blocks 2,832Bulk Pharma Intermediates 22 API Process Intermediates & Related Compounds 3,085

A selection we ship to Guatemala

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

Full pharmaceutical intermediates range

4-Iodobenzoic acid, 99%

CAS: 619-58-9
Formula: C₇H₅IO₂
MW: 248.02 g/mol

ZX-007410

4-Isopropylbenzoic acid, 98%

CAS: 536-66-3
Formula: C₁₀H₁₂O₂
MW: 164.2 g/mol

ZX-007411

4-Methoxycinnamic acid, ≥98%

CAS: 943-89-5
Formula: C₁₀H₁₀O₃
MW: 178.18 g/mol

ZX-007412

4-Methoxymandelic acid, 98%

CAS: 10502-44-0
Formula: C₉H₁₀O₄
MW: 182.17 g/mol

ZX-007413

4-Methoxyphenylacetic acid, 99%

CAS: 104-01-8
Formula: C₉H₁₀O₃
MW: 166.17 g/mol

ZX-007414

4-Methylphenylacetic acid, 98%

CAS: 622-47-9
Formula: C₉H₁₀O₂
MW: 150.17 g/mol

ZX-007415

4-Methylsalicylic acid, 99%

CAS: 50-85-1
Formula: C₈H₈O₃
MW: 152.15 g/mol

ZX-007416

4-Nitro-3-methoxybenzoic acid, 98%

CAS: 5081-36-7
Formula: C₈H₇NO₅
MW: 197.14 g/mol

ZX-007417

4-Nitrobenzoic acid, 99%

CAS: 62-23-7
Formula: C₇H₅NO₄
MW: 167.12 g/mol

ZX-007418

4-Nitrobenzoic acid, GR 99%+

CAS: 62-23-7
Formula: C₇H₅NO₄
MW: 167.12 g/mol

ZX-007419

4-Nitrophenylacetic acid, 98%

CAS: 104-03-0
Formula: C₈H₇NO₄
MW: 181.15 g/mol

ZX-007420

4-Nitrophthalic acid, 98%

CAS: 610-27-5
Formula: C₈H₅NO₆
MW: 211.13 g/mol

ZX-007421

Questions

Pharmaceutical Intermediates for Guatemala

Do you ship pharma intermediates 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 pharma intermediates 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.

Can you scale an intermediate from grams to kilograms without changing the route?

For many listed intermediates the gram packs and the kilogram supply come from the same manufacturing route, which keeps the impurity profile consistent. Where scale-up needs a different route, we tell you before you commit and can provide comparison samples so your team can check the new material against the old.

How do you control isomer and enantiomer content?

Positional isomers are controlled by HPLC or GC methods suited to the compound, and chiral intermediates are tested by chiral HPLC to report enantiomeric excess. The limits that apply to your lot appear on the COA. If your process needs tighter limits, state them on the enquiry and we will confirm what can be met.

Other divisions for Guatemala

Lab Reagents Solvents (HPLC & GC) Biochemicals APIs Impurity Reference Standards Inorganics & Metals Specialty Chemicals

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