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Japan · Pharmaceutical Intermediates

Pharma Intermediates supply to Japan

Buyers in Japan can order any of the 14,468 products in our pharmaceutical intermediates division. Locally, the main users are in pharmaceuticals, electronics & semiconductor materials and automotive. Typical delivery points include Tokyo / Kanagawa, Osaka (Doshomachi) and Toyama. Typical customers for this division are API manufacturers, CDMOs and CMOs and medicinal and discovery chemistry groups.

14,468products in this division
20–30 dsea transit from India
3–5 dair freight
4categories

Supplying pharmaceutical intermediates to Japan

Sea freight reaches Tokyo and Yokohama in about 20–30 days port to port. Urgent or small lots fly to Tokyo Narita (NRT) in 3–5 days. Import compliance for this category sits with PMDA / MHLW, 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 Japan

AuthorityPMDA / MHLW
SeaportsTokyo, Yokohama, Kobe
AirportsTokyo Narita (NRT), Osaka Kansai (KIX)
Dangerous goodsIMDG by sea, IATA DGR by air

New chemical substances must be notified under the Chemical Substances Control Law (CSCL), administered jointly by METI, MHLW and MOE, and importers report annual volumes of existing substances. The Industrial Safety and Health Act (ISHL) requires Japanese-language SDS and labels for listed substances, prepared by the importer. APIs need registration in the Japanese Drug Master File system with PMDA and foreign manufacturer accreditation. Dangerous goods follow IMDG or IATA rules, and CEPA preference requires a certificate of origin.

From order to delivery

  1. 1–2 daysQuote and document set agreed

    Price, pack sizes, Incoterm and the paperwork list are confirmed in writing.

  2. 3–7 daysPacking for export

    Stock items are packed in UN-rated drums or cartons. Made-to-order material adds its own lead time.

  3. 1–3 daysExport clearance at Nhava Sheva or Mundra

    Shipping bill filed, dangerous goods declared under IMDG where needed.

  4. 20–30 daysOcean transit to Tokyo

    Port-to-port time depends on the vessel schedule and any transhipment.

  5. 2–5 daysImport clearance

    Your broker clears the goods against local rules. Chemical oversight: METI / MHLW / MOE (CSCL), MHLW (ISHL).

Indicative total by sea: 27–47 days

By air: about 7–15 days in total.

Documents for Japan

  • Commercial Invoice
  • Packing List
  • Bill of Lading / Air Waybill
  • Certificate of Origin
  • Certificate of Analysis (COA)
  • Safety Data Sheet (16-section GHS)
  • CSCL existing-substance confirmation or new substance notification
  • Japanese-language SDS / label under ISHL (prepared by importer)
  • PMDA foreign manufacturer accreditation / Japanese DMF reference for APIs where applicable
  • Dangerous Goods Declaration (IMDG/IATA) where applicable

A selection we ship to Japan

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

Full pharmaceutical intermediates range
Questions

Pharmaceutical Intermediates for Japan

Can Zemixal deliver pharmaceutical intermediates to Japan?
Yes. We ship by sea to Tokyo and Yokohama, 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 Japan?
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 PMDA / MHLW is agreed with you at quote stage.
How long does delivery to Japan take?
Allow 20–30 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 Japan

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