Sodium Metasilicate

Please note, this OEL/ADE monograph also applies to Sodium metasilicate anhydrous (CAS RN 1344-09-8), Sodium metasilicate pentahydrate (CAS RN 10213-79-3), and Sodium metasilicate nonahydrate (CAS RN 13517-24-3). Sodium metasilicate, also known as sodium silicate and water glass, is an inorganic sodium salt having silicate as the counterion. Due to the equimolar ratio SiO2/Na2O (molar ratio (MR) = 1), sodium metasilicate has a regular crystalline structure. Sodium metasilicate is a soluble silicate and has a crystalline structure with pentahydrate and nonahydrate differing from the anhydrous form only by their water of crystallization. Sodium metasilicate is a versatile ingredient that can be used as an adhesive, corrosion inhibitor, and sealant, in cements and drilling fluids, for fireproofing wood, paper, and fabric, as a detergent booster, in wastewater treatment, and as shell coating to preserve eggs. It is often used in hair color and as a corrosion inhibitor in cosmetics; it is also used in shaving, bath, and oral hygiene products. Sodium metasilicate is the main component of commercial sodium silicate solutions.

Affygility Solutions has an occupational exposure limit (OEL) and control band assignment for this active pharmaceutical ingredient (API). This monograph also contains the acceptable daily exposure (ADE) value.

Sodium Metasilicate

CAS Registry Number:
6834-92-0
Cost:
$989 USD

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Why do you need this OEL Fastrac monograph?

OEL Fastrac monographs are a cost-effective and convenient way to meet the requirements for PDEs (ADEs) contained in the EMA Guideline on setting health based exposure limits for use in risk identification in the manufacture of different medicinal products in shared facilities (EMA/CHMP/CVMP/SWP/169430/2012), as well as PIC/S and ANVISA requirements, and to obtain the following information:

  • The numerical OEL and control band assignment needed to determine the level of required engineering controls and personal protective equipment
  • A listing of all cited references utilized in the derivation of the OEL and ADE
  • An expert review and discussion with respect to the critical endpoints of concern, the rationale for the choice of endpoints, and dose that is to be used in the derivation of the ADE (PDE), as required by the EMA's Guideline on setting health-based exposure limits for use in risk identification in the manufacture of different medicinal products in shared facilities

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  • Fully documented. Over 20 pages in length, with calculations and cited references.
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  • Director of Manufacturing