[Federal Register: April 6, 2005 (Volume 70, Number 65)]
[Notices]
[Page 17452-17453]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr06ap05-79]
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ENVIRONMENTAL PROTECTION AGENCY
[OPPT-2005-0017; FRL-7707-4]
Approval of Test Marketing Exemption for a Certain New Chemical
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
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SUMMARY: This notice announces EPA's approval of an application for
test marketing exemption (TME) under section 5(h)(1) of the Toxic
Substances Control Act (TSCA) and 40 CFR 720.38. EPA has designated
this application as TME-05-0001. The test marketing conditions are
described in the TME application and in this notice.
DATES: Approval of this TME is effective March 24, 2005.
FOR FURTHER INFORMATION CONTACT: For general information contact: Colby
Lintner, Regulatory Coordinator, Environmental Assistance Division
(7408M), Office of Pollution Prevention and Toxics, Environmental
Protection Agency, 1200 Pennsylvania Ave., NW., Washington, DC 20460-
0001; telephone number: (202) 554-1404; e-mail address:
TSCA-Hotline@epa.gov.
For technical information contact: Virginia Lee, Chemical Control
Division (7405M), Office of Pollution Prevention and Toxics,
Environmental Protection Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460-0001; telephone number: (202) 564-0883; e-mail
address: lee.virginia@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this Action Apply to Me?
This action is directed in particular to the chemical manufacturer
and/or importer who submitted the TME to EPA. This action may, however,
be of interest to the public in general. Since other entities may also
be interested, the Agency has not attempted to describe all the
specific entities that may be affected by this action. If you have any
questions regarding the applicability of this action to a particular
entity, consult the technical person listed under FOR FURTHER
INFORMATION CONTACT.
B. How Can I Get Copies of this Document and Other Related Information?
1. Docket. EPA has established an official public docket for this
action under docket identification (ID) number OPPT-2005-0017. The
official public docket consists of the documents specifically
referenced in this action, any public comments received, and other
information related to this action. Although a part of the official
docket, the public docket does not include Confidential Business
Information (CBI) or other information whose disclosure is restricted
by statute. The official public docket is the collection of materials
that is available for public viewing at the EPA Docket Center, Rm.
B102-Reading Room, EPA West, 1301 Constitution Ave., NW., Washington,
DC. The EPA Docket Center is open from 8:30 a.m. to 4:30 p.m., Monday
through Friday, excluding legal holidays. EPA Docket Center Reading
Room telephone number is (202) 566-1744 and the telephone number for
the OPPT Docket, which is located in EPA Docket Center, is (202) 566-
0280.
2. Electronic access. You may access this Federal Register document
electronically through the EPA Internet under the ``Federal Register''
listings at http://www.epa.gov/fedrgstr/.
An electronic version of the public docket is available through
EPA's electronic public docket and comment system, EPA Dockets. You may
use EPA Dockets at http://www.epa.gov/edocket/ to submit or view public
comments, access the index listing of the contents of the official
public docket, and to access those documents in the public docket that
are available electronically. Although, not all docket materials may be
available electronically, you may still access any of the publicly
available docket materials through the docket facility identified in
Unit I.B.1. Once in the system, select ``search,'' then key in the
appropriate docket ID number.
II. What is the Agency's Authority for Taking this Action?
Section 5(h)(1) of TSCA and 40 CFR 720.38 authorizes EPA to exempt
persons from premanufacture notification (PMN) requirements and permit
them to manufacture or import new chemical substances for test
marketing purposes, if the Agency finds that the manufacture,
processing, distribution in commerce, use, and disposal of the
substances for test marketing purposes will not present an unreasonable
risk of injury to health or the environment. EPA may impose
restrictions on test marketing activities and may modify or revoke a
test marketing exemption upon receipt of new information which casts
significant doubt on its finding that the test marketing activity will
not present an unreasonable risk of injury.
III. What Action is the Agency Taking?
EPA approves the above-referenced TME. EPA has determined that test
marketing the new chemical substance, under the conditions set out in
the TME application and in this notice, will not present any
unreasonable risk of injury to health or the environment.
IV. What Restrictions Apply to this TME?
The test market time period, production volume, number of
customers, and use must not exceed specifications in the application
and this notice. All other conditions and restrictions described in the
application and in this notice must also be met.
TME-05-0001
Date of receipt: February 7, 2005.
[[Page 17453]]
Notice of receipt: March 14, 2005, (70 FR 12478) (FRL-7704-9).
Applicant: PPG Industries, Inc..
Chemical: Alkanediocic acid, polymer with 1,3,5-tris(substituted
alkyl)-1,3,5-triazine-2,4,6(1H,3H,5H)-trione, alkanotate (ester) 3-
substituted-2-(substituted alkyl)-2-alkanoate (ester).
Use: Component of an automotive refinish direct-gloss topcoat.
Production volume: 5,000 kilogram/year (kg/yr).
Number of customers: 50.
Test marketing period: 365 days, commencing on first day of
commercial manufacture.
The following additional restrictions apply to this TME. A bill of
lading accompanying each shipment must state that the use of the
substance is restricted to that approved in the TME. In addition, the
applicant shall maintain the following records until 5 years after the
date they are created, and shall make them available for inspection or
copying in accordance with section 11 of TSCA:
1. Records of the quantity of the TME substance produced and the
date of manufacture.
2. Records of dates of the shipments to each customer and the
quantities supplied in each shipment.
3. Copies of the bill of lading that accompanies each shipment of
the TME substance.
V. What was EPA's risk assessment for this TME?
EPA identified no significant health or environmental concerns for
the test market substance. Therefore, the test market activities will
not present any unreasonable risk of injury to human health or the
environment.
VI. Can EPA Change Its Decision on this TME in the Future?
Yes. The Agency reserves the right to rescind approval or modify
the conditions and restrictions of an exemption should any new
information that comes to its attention cast significant doubt on its
finding, that the test marketing activities will not present any
unreasonable risk of injury to human health or the environment.
List of Subjects
Environmental protection, Test marketing exemptions.
Dated: March 24, 2005.
Miriam Wiggins-Lewis,
Acting Chief, New Chemicals Prenotice Management Branch, Office of
Pollution Prevention and Toxics.
[FR Doc. 05-6628 Filed 4-5-05 8:45 am]
BILLING CODE 6560-50-S