Zano® D is manufactured and tested in compliance with GMP Part II / ICH Q7 requirements. It undergoes testing using EP/USP analytical methods or validated in-house methods, ensuring compliance with specified standards. Zano® D is not suitable for UV applications.

INCI Name: Zinc Oxide

Labeling Claims: Not Listed In California Proposition 65

Certifications & Compliance: GMP, ISO 14001, ISO 9001, United States Pharmacopeia (USP)

Enhanced TDS

Identification & Functionality

Features & Benefits

Properties

Physical Form
Soluble In
Appearance
Soft, white or faintly yellowish-white, amorphous powder, free from gritty particles.
Soluble in
Mineral acids
Insoluble in
Water, Ethanol (96 per cent)
SDS Physical and Chemical Properties
ValueUnitsTest Method / Conditions
Molecular Weight81.39g/mol-
Density5.61g/cc-
Melting Point1975°C-
OdorOdorless--
AppearanceWhite Solid Powder--
Specifications
ValueUnitsTest Method / Conditions
Specific Surface Area (after production)min. 33.0m²/gBET
Aluminium Contentmax. 0.0020%ICP-AES
Loss on Ignitionmax. 1.0%EP/USP
Thallium Contentmax. 0.0005%ICP-AES
Arsenic Contentmax. 0.0002%ICP-AES
Iron Contentmax. 0.0050%ICP-AES
Cadmium Contentmax. 0.0005%ICP-AES
Lead Contentmax. 0.0010%ICP-AES
Zinc Oxide Content99.0 - 100.5%EP/USP

Regulatory & Compliance

Packaging & Availability

Packaging Type
Packaging Information

20 kg bags in cardboard box