Zano® 10 is manufactured and tested in compliance with GMP Part II / ICH Q7 requirements. It is tested using EP/USP analytical methods or validated in-house methods to ensure compliance with specified standards. This product is available in powder form and is soluble in dilute mineral acids. Zano® 10 is certified under ISO 9001, ISO 14001, and GMP standards, and complies with SARA 313 and United States Pharmacopeia (USP) requirements. It is not listed in California Proposition 65 and is compliant with global chemical inventories, including ISHL (Japan), KECI (Korea), ENCS (Japan), PICCS (Philippines), NZIoC (New Zealand), IECSC (China), and DSL (Canada). Zano® 10 is packaged in boxes for convenient handling and distribution.

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
Dilute Mineral Acids
Insoluble in
Water, Ethanol
SDS Physical and Chemical Properties
ValueUnitsTest Method / Conditions
Molecular Weight81.39g/mol-
Insoluble inWater--
Density5.61g/cc-
Melting Point1975°C-
OdorOdorless--
AppearanceWhite Solid Powder--
Specifications
ValueUnitsTest Method / Conditions
Specific Surface Areamin. 25m²/gBET
Chromium Contentmax. 0.0002%ICP-AES
Nickel Contentmax. 0.0010%ICP-AES
Aluminium Contentmax. 0.0050%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
  • 12.5 -20 kg bags in cardboard box