New Zealand · Impurity Reference Standards

Impurity Reference Standards for New Zealand

The impurity reference standards division counts 20,060 products, and each one can be quoted for delivery to New Zealand. Demand there comes mainly from dairy & food processing, agriculture & horticulture and forestry & wood products. Typical delivery points include Auckland, Tauranga / Bay of Plenty and Hamilton / Waikato. Typical customers for this division are pharma QC and analytical development labs, regulatory affairs teams and contract research organisations.

New Zealand Sample products

20,060products in this division

28–40 dsea transit from India

4–7 dair freight

6categories

Supplying impurity reference standards to New Zealand

Sea freight reaches Auckland and Tauranga in about 28–40 days port to port. Urgent or small lots fly to Auckland (AKL) in 4–7 days. Import compliance for this category sits with Medsafe, 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 New Zealand

Authority	Medsafe
Seaports	Auckland, Tauranga, Lyttelton
Airports	Auckland (AKL), Christchurch (CHC)
Dangerous goods	IMDG by sea, IATA DGR by air

Hazardous substances imported into New Zealand need an approval under the Hazardous Substances and New Organisms (HSNO) Act, usually through an EPA group standard, and importers must follow EPA notification and SDS rules. Medicines and APIs are regulated by Medsafe, and controlled drugs and precursors need Ministry of Health licences. Packaging and pallets are subject to MPI biosecurity requirements, including ISPM-15 treated timber. Dangerous goods follow IMDG or IATA rules.

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.
28–40 daysOcean transit to Auckland
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: EPA (HSNO Act).

Indicative total by sea: 35–57 days

By air: about 8–17 days in total.

Documents for New Zealand

Commercial Invoice
Packing List
Bill of Lading / Air Waybill
Certificate of Origin
Certificate of Analysis (COA)
Safety Data Sheet (16-section GHS)
HSNO approval / group standard assignment (importer)
Medsafe / Ministry of Health licence for medicines or controlled substances where applicable
MPI biosecurity packaging declaration (ISPM-15 timber) 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 New Zealand

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

Full impurity reference standards range

Nintedanib Impurity C

CAS: 2519501-85-8
Formula: C₂₃H₁₈N₂O₄
MW: 386.4 g/mol

ZX-005017

Nintedanib Impurity D

CAS: 1139455-52-9
Formula: C₃₂H₃₅N₅O₄
MW: 553.7 g/mol

ZX-005018

Nintedanib Impurity E

CAS: 2380229-45-6
Formula: C₃₃H₃₅N₅O₅
MW: 581.7 g/mol

ZX-005019

Nintedanib Impurity E (n-1)

CAS: 1253769-13-9
Formula: C₂₀H₁₇NO₅
MW: 351.4 g/mol

ZX-005020

Nintedanib Impurity F

CAS: 2410284-90-9
Formula: C₅₆H₅₂N₈O₈
MW: 965.1 g/mol

ZX-005021

Nintedanib Impurity F (Intermediate)

CAS: 2410649-54-4
Formula: C₂₂H₂₆N₆O₆
MW: 470.5 g/mol

ZX-005022

Nintedanib Methyl Impurity

CAS: 2734410-06-9
Formula: C₃₂H₃₅N₅O₄
MW: 553.7 g/mol

ZX-005023

Niraparib Methyl Ester Impurity

CAS: 2244220-34-4
Formula: C₂₀H₂₁N₃O₂
MW: 335.4 g/mol

ZX-005024

Nisoldipine Impurity A

CAS: 21829-25-4
Formula: C₁₇H₁₈N₂O₆
MW: 346.3 g/mol

ZX-005025

Nitrofurantoin Related Compound A

CAS: 63981-22-6
Formula: C₈H₈N₄O₆
MW: 256.17 g/mol

ZX-005026

Norelgestromin (E&Z Mixture)

CAS: 53016-31-2
Formula: C₂₁H₂₉NO₂
MW: 327.5 g/mol

ZX-005027

Obeticholic Acid Dimer Impurity

CAS: 1908444-28-9
Formula: C₅₂H₈₆O₇
MW: 823.2 g/mol

ZX-005028

Questions

Impurity Reference Standards for New Zealand

Can Zemixal deliver impurity reference standards to New Zealand?

Yes. We ship by sea to Auckland and Tauranga, 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 New Zealand?

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 Medsafe is agreed with you at quote stage.

How long does delivery to New Zealand take?

Allow 28–40 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.

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 New Zealand

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

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