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| Record Type: |
Domestic Substances List / Non-Confidential |
| CAS Registry Number: |
237753-63-8 |
| DSL/NDSL Record Number: |
72549 |
- Substance Name:
- Alcohols, C13-15, reaction products with N-[3-(dimethoxymethylsilyl)-2-methylpropyl]-1,2-ethanediamine, glycidol, and hydroxyterminated di-Me siloxanes
| Registration Number: |
SOR/2008-16, Order 2007-87-10-01 |
| Registration Date: |
12/20/2007 |
| Gazette Date: |
01/09/2008 |
- CEPA Reporting Requirements:
- Any activity involving Alcohols, C13-15, reaction products with N-[3-(dimethoxymethylsilyl)-2-methylpropyl]-1,2-ethanediamine, glycidol, and
hydroxyterminated di-Me siloxanes other than importing it or distributing it for
(a) industrial use as a paper softener in the treatment of sanitary tissue in quantities less than 150 000 kilograms of the substance per year, per site of use, and where effluents receive secondary or an equivalent wastewater treatment;
(b) industrial use as a fabric softener in the treatment of textiles in quantities less than 25 000 kilograms of the substance per year, per site of use, and where effluents receive secondary or an equivalent wastewater treatment;
(c) industrial use of the substance in a non-aqueous system if the substance is not released into wastewater; or
(d) use of the substance in personal care products that are not applied as a spray or aerosol.
The following information must be provided to the Minister, at least 90 days before the commencement of the proposed new activity:
(a) a description of the proposed significant new activity in relation to the substance;
(b) the information specified in Schedule 9 to the New Substances Notification Regulations (Chemicals and Polymers);
(c) the information specified in item 5 of Schedule 10 to those Regulations;
(d) the concentration of the substance in the final product as a result of the significant new activity; and
(e) for use of the substance in personal care products that are applied as a spray or aerosol,
(i) the particle size distribution of the substance in the final product as a result of the significant new activity; and
(ii) test data form a 90-day inhalation study conducted according to the methodology described in OECD Test Guideline No. 413 entitled Subchronic Inhalation Toxicity: 90-day Study and in conformity with the practices described in the "OECD Principles of Good Laboratory Practice" set out in Annex 2 of the Decision of the Council Concerning the Mutual Acceptance of Data in the Assessment of Chemicals, adopted on May 12, 1981, and that are current at the time the test date are developed or any other information that will permit the assessment of the inhalation toxicity of the substance.
The above information will be assessed within 90 days after it is received by the Minister.
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- This database is prepared only as a guide and has no legal authority. Refer to the Canadian Environmental Protection Act (CEPA) and its regulations as the final authority.
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- This database contains amendments, additions, and deletions
published in the Canada Gazette up to and including September 15, 2012.
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©2010 Canadian Centre for Occupational Health & Safety 