Purity Sample Clauses
The Purity clause establishes standards or requirements regarding the absence of contaminants or unwanted substances in goods or materials provided under a contract. Typically, it specifies acceptable levels of purity, outlines testing methods, or sets forth certification requirements to ensure compliance. This clause is essential for ensuring product quality and safety, particularly in industries such as pharmaceuticals, food, or chemicals, and helps prevent disputes by clearly defining what constitutes an acceptable product.
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Purity. Comprised of at least ninety-five percent (95%) by volume of CO2.
Purity. [**] [**] [**]
Purity. All Liquid Helium delivered hereunder shall have a purity of not less than 99.999% Helium by volume in accordance with Compressed Gas Association Helium Specification G-9.1
Purity. Novex SDS-electrophoresis (4-20% gel) Coomassie blue 60805C Report result. Target specification: Report result as % purity and comparison to reference
Purity. 3.1. Product related substances and impurities by RP-HPLC Reversed phase chromatography (RP-HPLC) [***]
3.1.1 Product related substances (deamidated, succinimide, oxidized) Reversed phase chromatography (RP-HPLC) [***]
3.1.2 Product related impurities (clipped and other variants) Reversed phase chromatography (RP-HPLC) [***]
Purity. On a plate basis the average purity of Compounds shall be at least [***]%, with no Compounds being less then [***]% pure. Chemical identity and overall purity of each Compound ([***]) WITH [***] compliance should be provided by Array with analytical data on CD ROM. Pfizer shall have an opportunity to review this analytical information prior to selecting each Library. Pfizer shall have no obligation to incur any cost for, or to accept any Compound for which these data are not provided or which do not support structural confirmation or which otherwise fail to meet the specifications set forth in this exhibit, unless otherwise agreed by both Parties in writing, provided also that such a defect will be reported by Pfizer within 30 days from the receipt of non-conforming Compounds, otherwise, such Compounds shall be deemed satisfactory. Array 's liability for providing non-conforming Compounds to either replacing it with a conforming Compound or, at Pfizer's discretion, promptly refunding the purchase price paid, if any, for non-conforming Compounds.
Purity. Subject to the provision by Sunoco of Boiler Feed Water which meets the Boiler Feed Water Standards, Haverhill shall provide a maximum 0.5 PPM sodium carryover at each HRSG.
Purity. Goldmoney accounting units of Gold, in accordance with standard bullion-market practice, are expressed in fine Gold content. The fine Gold content of each bar equals its weight multiplied by its purity. The resulting units of Gold in your Goldmoney Personal or Business Account are 100% pure Gold and denominated in kilograms and grams. Goldmoney confirms that it has obtained a representation from its Gold bullion counterparties that every gram of Gold purchased by Goldmoney to be sold to Users is a gram of the 100% pure Gold content (fine Gold) of a 99.5% (or greater) assayed bullion bar held in the relevant vault.
Purity. Gold Farm accounting units of precious metals, in accordance with standard bullion-market practice, are expressed in fine precious metal content. The fine precious metal content of each bar equals its weight multiplied by its purity. The resulting units of precious metals in your Gold Farm Account are 100% pure and denominated in and grams and ▇▇▇▇ ounces. Gold Farm confirms that it has obtained a representation from its precious metals bullion counterparties that every gram or ▇▇▇▇ ounce purchased by Gold Farm to be sold to Users is a gram or ▇▇▇▇ ounce of the 100% pure content of a 99.5% (or greater) assayed bullion bar held in the relevant vault.
Purity. A. HPLC [ * ] of reference standard by peak area
B. Loss on Drying [ * ] by weight