Vietnam · Pharmaceutical Intermediates

Pharmaceutical Intermediates shipped to Vietnam

Zemixal supplies 14,468 products from its pharmaceutical intermediates range to buyers in Vietnam. In Vietnam the strongest demand is from textiles & garments, electronics assembly and generic pharmaceuticals. Typical delivery points include Ho Chi Minh City, Binh Duong and Dong Nai. Typical customers for this division are API manufacturers, CDMOs and CMOs and medicinal and discovery chemistry groups.

Vietnam Sample products

14,468products in this division

14–22 dsea transit from India

3–5 dair freight

4categories

Supplying pharmaceutical intermediates to Vietnam

Sea freight reaches Ho Chi Minh City (Cat Lai) and Cai Mep–Thi Vai in about 14–22 days port to port. Urgent or small lots fly to Ho Chi Minh City Tan Son Nhat (SGN) in 3–5 days. Import compliance for this category sits with DAV (Drug Administration of Vietnam, Ministry of Health), and we prepare the COA, SDS and commercial documents your broker needs. 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 Vietnam

Authority	DAV (Drug Administration of Vietnam, Ministry of Health)
Seaports	Ho Chi Minh City (Cat Lai), Cai Mep–Thi Vai, Hai Phong
Airports	Ho Chi Minh City Tan Son Nhat (SGN), Hanoi Noi Bai (HAN)
Dangerous goods	IMDG by sea, IATA DGR by air

Under the Law on Chemicals and its decrees, many industrial chemicals need an import chemical declaration through the National Single Window, and restricted or precursor chemicals may require an MOIT licence administered by the Vietnam Chemicals Agency. APIs and pharmaceutical raw materials are controlled by the Drug Administration of Vietnam and usually need registration or an import licence. Vietnamese-language SDS or labels may be requested. Dangerous goods follow IMDG or IATA rules, and AITIGA preference requires a certificate of origin.

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.
14–22 daysOcean transit to Ho Chi Minh City (Cat Lai)
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: MOIT – Vietnam Chemicals Agency (Law on Chemicals).

Indicative total by sea: 21–39 days

By air: about 7–15 days in total.

Documents for Vietnam

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
Chemical import declaration via National Single Window (MOIT) where applicable
DAV import licence / registration for APIs where applicable
Vietnamese-language SDS / label where required
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 Vietnam

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

Full pharmaceutical intermediates range

3-Chloropyridazine Hydrochloride

CAS: 856847-77-3
Formula: C₄H₄Cl₂N₂
MW: 150.99 g/mol

ZX-041374

Stearoyl Ethanolamide

CAS: 111-57-9
Formula: C₂₀H₄₁NO₂
MW: 327.5 g/mol

ZX-041377

4-(tert-Butyl)cyclohexyl Acrylate

CAS: 84100-23-2
Formula: C₁₃H₂₂O₂
MW: 210.31 g/mol

ZX-041378

(2E)-N-(4-Fluorophenyl)-3-phenylprop-2-enamide

CAS: 19358-27-1
Formula: C₁₅H₁₂FNO
MW: 241.26 g/mol

ZX-041379

Tris(2-chloropropyl) phosphate

CAS: 6145-73-9
Formula: C₉H₁₈Cl₃O₄P
MW: 327.6 g/mol

ZX-041381

H-D-Phe-Pip-Arg-pNA dihydrochloride

CAS: 62354-65-8
Formula: C₂₇H₃₈Cl₂N₈O₅
MW: 625.5 g/mol

ZX-041382

Ethylene Terephthalate Cyclic Pentamer

CAS: 16104-97-5
Formula: C₅₀H₄₀O₂₀
MW: 960.8 g/mol

ZX-041383

3,6,9,13,16,19-Hexaoxa-1,11(1,4)-dibenzenacycloicosaphane-2,10,12,20-tetraone

CAS: 16104-98-6
Formula: C₂₄H₂₄O₁₀
MW: 472.4 g/mol

ZX-041384

3,6,10,13,16-Pentaoxa-1,8(1,4)-dibenzenacycloheptadecaphane-2,7,9,17-tetraone

CAS: 29278-57-7
Formula: C₂₂H₂₀O₉
MW: 428.4 g/mol

ZX-041385

Steppogenin

CAS: 56486-94-3
Formula: C₁₅H₁₂O₆
MW: 288.25 g/mol

ZX-041386

4,4`-Bis (Dimethylamino) benzophenone

CAS: 90-94-8
Formula: C₁₇H₂₀N₂O
MW: 268.35 g/mol

ZX-041387

Xanthopterin

CAS: 119-44-8
Formula: C₆H₅N₅O₂
MW: 179.14 g/mol

ZX-041388

Questions

Pharmaceutical Intermediates for Vietnam

Can Zemixal deliver pharmaceutical intermediates to Vietnam?

Yes. We ship by sea to Ho Chi Minh City (Cat Lai) and Cai Mep–Thi Vai, 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 Vietnam?

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 DAV (Drug Administration of Vietnam, Ministry of Health) is agreed with you at quote stage.

How long does delivery to Vietnam take?

Allow 14–22 days for ocean transit or 3–5 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 Vietnam

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

Pharmaceutical Intermediates in nearby countries