Cambodia · Impurity Reference Standards

Impurity Reference Standards shipped to Cambodia

The impurity reference standards division counts 20,060 products, and each one can be quoted for delivery to Cambodia. Locally, the main users are in garments & footwear, construction materials and food & beverage. Typical delivery points include Phnom Penh, Sihanoukville SEZ and Kandal. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

Cambodia Sample products

20,060products in this division

16–24 dsea transit from India

3–6 dair freight

6categories

Supplying impurity reference standards to Cambodia

Sea freight reaches Sihanoukville and Phnom Penh Autonomous Port in about 16–24 days port to port. Urgent or small lots fly to Phnom Penh Techo (KTI) in 3–6 days. Import compliance for this category sits with Department of Drugs and Food (DDF), Ministry of Health, and we prepare the COA, SDS and commercial documents your broker needs. 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 Cambodia

Authority	Department of Drugs and Food (DDF), Ministry of Health
Seaports	Sihanoukville, Phnom Penh Autonomous Port
Airports	Phnom Penh Techo (KTI), Siem Reap–Angkor (SAI)
Dangerous goods	IMDG by sea, IATA DGR by air

Industrial chemicals are overseen mainly by the Ministry of Industry, Science, Technology and Innovation (MISTI), and hazardous or precursor chemicals may need an import permit before customs clearance through the ASYCUDA system. Medicines and APIs require registration and import authorisation from the Department of Drugs and Food at the Ministry of Health. Dangerous goods follow IMDG or IATA rules. AITIGA preference requires a certificate of origin, which we can issue for eligible goods.

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.
16–24 daysOcean transit to Sihanoukville
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: Ministry of Industry, Science, Technology & Innovation (MISTI).

Indicative total by sea: 23–41 days

By air: about 7–16 days in total.

Documents for Cambodia

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
MISTI import permit for hazardous / controlled chemicals where applicable
DDF import authorisation for medicines / APIs 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 Cambodia

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

Full impurity reference standards range

Encorafenib Amino Carbamate Impurity

CAS: 1269440-78-9
Formula: C₂₁H₂₅ClFN₇O₂
MW: 461.9 g/mol

ZX-024505

(E/Z)-Ensifentrine

CAS: 298680-25-8
Formula: C₂₆H₃₁N₅O₄
MW: 477.6 g/mol

ZX-024506

Entacapone Amide Impurity

CAS: 158693-01-7
Formula: C₁₀H₇N₃O₅
MW: 249.18 g/mol

ZX-024507

1R,3R,4R Entecavir

CAS: 1367369-76-3
Formula: C₁₂H₁₅N₅O₃
MW: 277.28 g/mol

ZX-024508

2-Amino-9-((1S,3R,4R)-4-(benzyloxy)-3-((benzyloxy)methyl)-2-methylenecyclopentyl)-1,9-dihydro-6H-purin-6-one

CAS: 1354695-85-4
Formula: C₂₆H₂₇N₅O₃
MW: 457.5 g/mol

ZX-024509

[1S-(1α,2α,3β,5α)]-3-(Phenylmethoxy)-2-[(phenylmethoxy)methyl]-6-oxabicyclo[3.1.0]hexane

CAS: 110567-22-1
Formula: C₂₀H₂₂O₃
MW: 310.4 g/mol

ZX-024510

(1S,2S,3S,5S)-3-(Benzyloxy)-5-(6-(benzyloxy)-2-(((4-methoxyphenyl)diphenylmethyl)amino)-9H-purin-9-yl)-2-((benzyloxy)methyl)cyclopentan-1-ol

CAS: 142217-78-5
Formula: C₅₂H₄₉N₅O₅
MW: 824 g/mol

ZX-024511

4-Methylbenzylidene Camphor

CAS: 36861-47-9
Formula: C₁₈H₂₂O
MW: 254.4 g/mol

ZX-024512

Enzalutamide - Impurity A

CAS: 112704-79-7
Formula: C₇H₄BrFO₂
MW: 219.01 g/mol

ZX-024513

4-(3-(4-Cyano-3-(trifluoromethyl)phenyl)thioureido)-2-fluoro-N-methylbenzamide

CAS: 1798807-39-2
Formula: C₁₇H₁₂F₄N₄OS
MW: 396.4 g/mol

ZX-024514

Enzalutamide Impurity 47

CAS: 2029195-97-7
Formula: C₂₁H₁₈F₄N₄O₃
MW: 450.4 g/mol

ZX-024515

Enzalutamide Impurity D

CAS: 1332524-02-3
Formula: C₁₁H₁₂FNO₄
MW: 241.22 g/mol

ZX-024516

Questions

Impurity Reference Standards for Cambodia

Can Zemixal deliver impurity reference standards to Cambodia?

Yes. We ship by sea to Sihanoukville and Phnom Penh Autonomous Port, 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 Cambodia?

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 Department of Drugs and Food (DDF), Ministry of Health is agreed with you at quote stage.

How long does delivery to Cambodia take?

Allow 16–24 days for ocean transit or 3–6 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 Cambodia

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

Impurity Reference Standards in nearby countries