Standardized mitragynine, made at a regulated pharmaceutical facility.

Water-soluble and non-water-soluble extract, standardized to a declared mitragynine content — with laboratory-verified purity up to 97%. A member of the Biofarma Group.

SUBANG, WEST JAVA · SUPERVISED BY KEMENKES & BPOM · MEMBER OF BIOFARMA GROUP

Standardized kratom extract powder
The botanical

From Mitragyna speciosa leaf to a standardized extract.

Mitragyna speciosa (Korth.) Havil. is a tropical evergreen of the Rubiaceae family, native to Southeast Asia. Its leaf is rich in indole alkaloids, of which mitragynine is the most abundant.

Our extract concentrates that alkaloid from the dried leaf into a consistent, declared assay — so a downstream manufacturer receives a defined specification rather than variable raw botanical.

Fresh Mitragyna speciosa leaves
Product grades

Two extract families, four assay levels.

Each grade is standardized to a declared mitragynine content. The final assay for your order is confirmed at the contract stage.

Two kratom extract grades side by side
Standardized kratom extract, supplied in water-soluble and non-water-soluble grades.

Water-soluble

Mitragynine salt
60%70%80%≥90%

Highest assay achieved to date: 95%

Non-water-soluble

Mitragynine salt & free base
60%70%80%≥90%

Highest purity achieved to date: 97%

Verified purity & safety

Measured in our own laboratory.

Results below are the highest purity achieved on our 90%-up grade, confirmed by two independent methods, alongside acute-toxicity and heavy-metal testing.

97.72%
Mitragynine by GC-MS
97.28%
Mitragynine by HPLC
>5000
LD50 mg/kg — practically non-toxic
Pass
Heavy-metal contaminant panel

Figures represent highest purity achieved to date, not a guaranteed release specification. Release specification is confirmed per contract.

Specification & testing

Tested against pharmacopoeial limits.

Representative results for the 90%-up grade. Identity is confirmed by FTIR and NMR against a mitragynine reference.

ParameterMethod / limitResult
Mitragynine (identity)FTIR / NMR — matches referenceConfirmed
Loss on dryingUSP · ≤ 5%2.9%
Residue on ignitionUSP · ≤ 0.1%0.04%
Residual solvent — tolueneICH Q3C / USP · ≤ 890 ppm0.10 ppm
Residual solvent — benzeneICH Q3C / USP · ≤ 2 ppm0.004 ppm
Heavy metalsContaminant panelPass
Acute toxicityLD50, oral>5000 mg/kg

Values are representative test results, not guaranteed release figures. A certificate of analysis accompanies each shipment; the release specification is agreed at contract. A documented pharmacological profile is available to qualified B2B partners under separate cover.

The manufacturer

A regulated pharmaceutical facility.

PT Sinkona Indonesia Lestari manufacturing facility in Subang, West Java, with mountains behind
The Sinkona manufacturing complex in Ciater, Subang, West Java.

Supervised by Kemenkes & BPOM

PT Sinkona Indonesia Lestari operates a pharmaceutical manufacturing facility under the supervision of the Indonesian Ministry of Health (Kemenkes) and the National Agency of Drug and Food Control (BPOM). That supervision applies to our alkaloid production operation.

Kratom extract is manufactured within the same facility, using the same quality system, laboratory, and lot-release discipline. Regulatory registration specific to the kratom extract is confirmed per destination market at the contract stage.

Member of Biofarma Group

Part of Indonesia's state-owned pharmaceutical holding, alongside a heritage in cinchona alkaloid manufacturing.

Released per lot

Every lot is documented from intake to release, with a certificate of analysis and retained sample.

Export-ready

Established documentation and logistics from an operation that already exports pharmaceutical-grade alkaloids.

Contact

Request a quote or a sample.

CompanyPT Sinkona Indonesia Lestari
Ciater, Subang Regency, West Java, Indonesia

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