Draft Toxicological Review of Propionaldehyde: In Support of Summary Information on the Integrated Risk Information System, 24281-24282 [E8-9734]
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Federal Register / Vol. 73, No. 86 / Friday, May 2, 2008 / Notices
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Dated: April 29, 2008.
Robert W. Hargrove,
Director, NEPA Compliance Division, Office
of Federal Activities.
[FR Doc. E8–9744 Filed 5–1–08; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[FRL–8561–4; Docket ID No. EPA–HQ–ORD–
2008–0165]
Draft Toxicological Review of
Propionaldehyde: In Support of
Summary Information on the
Integrated Risk Information System
Environmental Protection
Agency (EPA).
ACTION: Notice of peer-review meeting.
mstockstill on PROD1PC66 with NOTICES
AGENCY:
SUMMARY: EPA is announcing that
Versar, Inc., an EPA contractor for
external scientific peer review, will
convene an independent panel of
experts and organize and conduct an
external peer-review meeting via
teleconference to review the external
review draft document titled,
‘‘Toxicological Review of
Propionaldehyde: In Support of
Summary Information on the Integrated
Risk Information System (IRIS)’’ (EPA/
635/R–08/003A). A 60-day public
VerDate Aug<31>2005
17:17 May 01, 2008
Jkt 214001
comment period for the draft document
was announced on March 6, 2008 (73
FR 12171–12172). The draft document
was prepared by the National Center for
Environmental Assessment (NCEA)
within EPA’s Office of Research and
Development. The public comment
period and the external peer-review
meeting are separate processes that
provide opportunities for all interested
parties to comment on the document.
EPA is releasing this draft document
solely for the purpose of predissemination peer review under
applicable information quality
guidelines. This document has not been
formally disseminated by EPA. It does
not represent and should not be
construed to represent any Agency
policy or determination.
Versar, Inc. invites the public to
register to attend this meeting as
observers. In addition, Versar, Inc.
invites the public to give oral and/or
provide written comments at the
meeting regarding the draft document
under review. The draft document and
EPA’s peer-review charge are available
primarily via the Internet on NCEA’s
home page under the Recent Additions
and the Data and Publications menus at
https://www.epa.gov/ncea. In preparing a
final report, EPA will consider the
Versar, Inc. report of the comments and
recommendations from the external
peer-review meeting and any public
comments that EPA receives.
DATES: The peer-review panel meeting
will begin on May 29, 2008, at 10:30
a.m. and end at 2:30 p.m. EST. As
announced on March 6, 2008 (73 FR
12171–12172), the 60-day public
comment period began March 6, 2008,
and ends May 5, 2008. Technical
comments should be in writing and
must be received by EPA by May 5,
2008.
ADDRESSES: The peer-review meeting
will be held via teleconference. The
EPA contractor, Versar, Inc., is
organizing, convening, and conducting
the peer-review meeting. To attend the
meeting, register by May 23, 2008, by
calling Versar, Inc. at 703–750–3000 ext.
316, sending a facsimile to 703–642–
6954, or sending an e-mail to
ssarraino@versar.com. You may also
register via the Internet at https://
epa.versar.com/propionaldehyde.
The draft ‘‘Toxicological Review of
Propionaldehyde: In Support of
Summary Information on the Integrated
Risk Information System (IRIS)’’ is
available primarily via the Internet on
the National Center for Environmental
Assessment’s home page under the
Recent Additions and the Data and
Publications menus at https://
PO 00000
Frm 00071
Fmt 4703
Sfmt 4703
24281
www.epa.gov/ncea. A limited number of
paper copies are available from the
Information Management Team, NCEA;
telephone: 703–347–8561; facsimile:
703–347–8691. If you are requesting a
paper copy, please provide your name,
mailing address, and the document title,
‘‘Toxicological Review of
Propionaldehyde: In Support of
Summary Information on the Integrated
Risk Information System (IRIS).’’ Copies
are not available from Versar, Inc.
FOR FURTHER INFORMATION CONTACT:
Questions regarding information,
registration, access or services for
individuals with disabilities, or logistics
for the external peer-review meeting
should be directed to Stephanie
Sarraino, Versar, Inc., Springfield, VA
22151; telephone: 703–750–3000 ext.
316; facsimile: 703–642–6954; e-mail
ssarraino@versar.com. To request
accommodation of a disability, please
contact Versar, Inc. preferably at least 10
days prior to the meeting, to give as
much time as possible to process your
request.
If you need technical information
about the document, please contact John
Stanek, National Center for
Environmental Assessment (NCEA);
telephone: 919–541–1048; facsimile:
919–541–0245; e-mail:
stanek.john@epa.gov.
SUPPLEMENTARY INFORMATION:
I. Summary of Information About the
Project/Document
The draft Toxicological Review of
Propionaldehyde is a new assessment
and provides scientific information on
the effects pertaining to exposure to
propionaldehyde. Propionaldehyde was
nominated by the EPA Office of Air and
Radiation in 2000 and 2001 and by the
Office of Air Quality Planning and
Standards in 2003 as a chemical listed
for monitoring under the Clean Air Act.
Propionaldehyde is a colorless liquid
with a suffocating, fruity odor. It is used
in the manufacturing of propionic acid
and polyvinyl and other plastics, in the
synthesis of rubber chemicals, and as a
disinfectant and preservative. The
chemical is released to the environment
primarily through the combustion of
wood, gasoline, diesel fuel, and
polyethylene. Propionaldehyde is also a
component of cigarette smoke and a
food additive/flavoring agent. Although
no studies on the effects of
propionaldehyde administered by the
oral route have been performed, based
on its expected daily intake (below 1800
ug/day) and eventual metabolism in the
citric acid cycle, it does not appear to
be a safety concern for public health via
ingestion. Thus, the most probable route
E:\FR\FM\02MYN1.SGM
02MYN1
24282
Federal Register / Vol. 73, No. 86 / Friday, May 2, 2008 / Notices
of exposure of concern to the general
population is by inhalation. The
assessment will present reference values
for the noncancer effects of
propionaldehyde (RfD and RfC), where
supported by available data, and a
cancer assessment.
II. Meeting Information
Members of the public may attend the
meeting as observers, and there will be
a limited time for comments from the
public. Please let Versar, Inc. know if
you wish to make comments during the
meeting. Space is limited, and
reservations will be accepted on a firstcome, first-served basis.
Dated: April 24, 2008.
Rebecca Clark,
Director, National Center for Environmental
Assessment.
[FR Doc. E8–9734 Filed 5–1–08; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OAR–2008–0321; FRL–8561–5]
Protection of Stratospheric Ozone:
Request for Critical Use Exemption
Applications for the Years 2010 and
2011
Environmental Protection
Agency (EPA).
ACTION: Notice of Solicitation of
Applications and Information on
Alternatives.
mstockstill on PROD1PC66 with NOTICES
AGENCY:
SUMMARY: EPA is soliciting applications
for the critical use exemption from the
phaseout of methyl bromide for 2011
and beyond. In addition, applicants who
missed last year’s deadline to submit a
critical use application for an exemption
in the year 2010 may file a
supplemental application in response to
this notice. This exemption is an annual
exemption and all entities interested in
obtaining a critical use exemption must
provide EPA with technical and
economic information to support a
‘‘critical use’’ claim and must do so by
the deadline specified in this notice
even if they have previously applied for
an exemption. Today’s notice also
invites interested parties to provide EPA
with new data on the technical and
economic feasibility of methyl bromide
alternatives.
DATES: Applications for the critical use
exemption must be postmarked on or
before July 31, 2008. The response
period reflects the clarifications and
reduction of burden in the application.
ADDRESSES: Applications for the methyl
bromide critical use exemption should
VerDate Aug<31>2005
17:17 May 01, 2008
Jkt 214001
be submitted in duplicate (two copies)
by mail to: U.S. Environmental
Protection Agency, Office of Air and
Radiation, Stratospheric Protection
Division, Attention Methyl Bromide
Review Team, Mail Code 6205J, 1200
Pennsylvania Ave., NW., Washington,
DC 20460 or by courier delivery (other
than U.S. Post Office overnight) to: U.S.
Environmental Protection Agency,
Office of Air and Radiation,
Stratospheric Protection Division,
Attention Methyl Bromide Review
Team, 1310 L St., NW., Room 1047E,
Washington, DC 20005. EPA also
encourages users to submit their
applications electronically to Jeremy
Arling, Stratospheric Protection
Division, at arling.jeremy@epa.gov. If
the application is submitted
electronically, applicants must fax a
signed copy of Worksheet 1 to Jeremy
Arling at 202–343–2338 by the
application deadline.
FOR FURTHER INFORMATION CONTACT:
General Information: U.S. EPA
Stratospheric Ozone Information
Hotline, 1–800–296–1996; also https://
www.epa.gov/ozone/mbr.
Technical Information: Colwell Cook,
U.S. Environmental Protection Agency,
Office of Pesticide Programs (7503P),
1200 Pennsylvania Ave., NW.,
Washington, DC 20460, 703–308–8146,
E-mail: cook.colwell@epa.gov.
Economic Information: Elisa Rim,
U.S. Environmental Protection Agency,
Office of Pesticide Programs (7503P),
1200 Pennsylvania Ave., NW.,
Washington, DC 20460, 703–308–8123,
E-mail: rim.elisa@epa.gov.
Regulatory Information: Jeremy
Arling, U.S. Environmental Protection
Agency, Stratospheric Protection
Division (6205J), 1200 Pennsylvania
Ave., NW., Washington, DC 20460, 202–
343–9055, E-mail:
arling.jeremy@epa.gov.
SUPPLEMENTARY INFORMATION:
Table of Contents
I. What do I need to know to respond to this
request for applications?
A. Who can respond to this request for
information?
B. Whom can I contact to find out if a
consortium is submitting an application
form for my methyl bromide use?
C. How do I obtain an application form for
the methyl bromide critical use
exemption?
D. What alternatives must applicants
address when applying for a critical use
exemption?
E. What portions of the applications will be
considered confidential business
information?
F. Must I submit a ‘‘Notice of Intent to
Apply?’’
G. What if I submit an incomplete
application?
PO 00000
Frm 00072
Fmt 4703
Sfmt 4703
H. What if I applied for a critical use
exemption in a previous year?
II. What is the legal authority for the critical
use exemption?
A. What is the Clean Air Act (CAA)
authority for implementing the critical
use exemption to the methyl bromide
phaseout?
B. What is the Montreal Protocol authority
for granting a critical use exemption after
the methyl bromide phaseout?
III. How is the U.S. implementing the critical
use exemption?
A. When will the exemption become
available to U.S. users of methyl
bromide?
B. What is the projected timeline for the
critical use exemption application
process?
I. What do I need to know to respond
to this request for applications?
A. Who Can Respond to This Request
for Information?
Entities interested in obtaining a
critical use exemption must complete
the application form available at
https://www.epa.gov/ozone/mbr. The
application form may be submitted
either by a consortium representing
multiple users who have similar
circumstances or by individual users
who anticipate needing methyl bromide
in 2011 and beyond and believe there
are no technically and economically
feasible alternatives. EPA encourages
groups of users with similar
circumstances of use to submit a single
application (for example, any number of
pre-plant users with similar soil, pest,
and climactic conditions can join
together to submit a single application).
In some instances, state agencies will
assist users with the application process
(see discussion of voluntary state
involvement in Part I.B. below). Given
that this is the seventh round of the
critical use exemption process, EPA will
take a skeptical view regarding
supporting new nominations (meaning,
specific applicants who have not
previously been nominated by the USG
for an exemption) unless the applicant
demonstrates that an unforeseeable
change in circumstances (e.g.,
withdrawal or significant change in
registration status of an alternative)
justifies the need.
In addition to requesting information
from applicants for the critical use
exemption, this solicitation for
information provides an opportunity for
any interested party to provide EPA
with information on methyl bromide
alternatives (e.g., technical and/or
economic feasibility research). The
application form for the methyl bromide
critical use exemption and other
information on research relevant to
alternatives must be sent to the
E:\FR\FM\02MYN1.SGM
02MYN1
Agencies
[Federal Register Volume 73, Number 86 (Friday, May 2, 2008)]
[Notices]
[Pages 24281-24282]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-9734]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[FRL-8561-4; Docket ID No. EPA-HQ-ORD-2008-0165]
Draft Toxicological Review of Propionaldehyde: In Support of
Summary Information on the Integrated Risk Information System
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice of peer-review meeting.
-----------------------------------------------------------------------
SUMMARY: EPA is announcing that Versar, Inc., an EPA contractor for
external scientific peer review, will convene an independent panel of
experts and organize and conduct an external peer-review meeting via
teleconference to review the external review draft document titled,
``Toxicological Review of Propionaldehyde: In Support of Summary
Information on the Integrated Risk Information System (IRIS)'' (EPA/
635/R-08/003A). A 60-day public comment period for the draft document
was announced on March 6, 2008 (73 FR 12171-12172). The draft document
was prepared by the National Center for Environmental Assessment (NCEA)
within EPA's Office of Research and Development. The public comment
period and the external peer-review meeting are separate processes that
provide opportunities for all interested parties to comment on the
document.
EPA is releasing this draft document solely for the purpose of pre-
dissemination peer review under applicable information quality
guidelines. This document has not been formally disseminated by EPA. It
does not represent and should not be construed to represent any Agency
policy or determination.
Versar, Inc. invites the public to register to attend this meeting
as observers. In addition, Versar, Inc. invites the public to give oral
and/or provide written comments at the meeting regarding the draft
document under review. The draft document and EPA's peer-review charge
are available primarily via the Internet on NCEA's home page under the
Recent Additions and the Data and Publications menus at https://
www.epa.gov/ncea. In preparing a final report, EPA will consider the
Versar, Inc. report of the comments and recommendations from the
external peer-review meeting and any public comments that EPA receives.
DATES: The peer-review panel meeting will begin on May 29, 2008, at
10:30 a.m. and end at 2:30 p.m. EST. As announced on March 6, 2008 (73
FR 12171-12172), the 60-day public comment period began March 6, 2008,
and ends May 5, 2008. Technical comments should be in writing and must
be received by EPA by May 5, 2008.
ADDRESSES: The peer-review meeting will be held via teleconference. The
EPA contractor, Versar, Inc., is organizing, convening, and conducting
the peer-review meeting. To attend the meeting, register by May 23,
2008, by calling Versar, Inc. at 703-750-3000 ext. 316, sending a
facsimile to 703-642-6954, or sending an e-mail to
ssarraino@versar.com. You may also register via the Internet at https://
epa.versar.com/propionaldehyde.
The draft ``Toxicological Review of Propionaldehyde: In Support of
Summary Information on the Integrated Risk Information System (IRIS)''
is available primarily via the Internet on the National Center for
Environmental Assessment's home page under the Recent Additions and the
Data and Publications menus at https://www.epa.gov/ncea. A limited
number of paper copies are available from the Information Management
Team, NCEA; telephone: 703-347-8561; facsimile: 703-347-8691. If you
are requesting a paper copy, please provide your name, mailing address,
and the document title, ``Toxicological Review of Propionaldehyde: In
Support of Summary Information on the Integrated Risk Information
System (IRIS).'' Copies are not available from Versar, Inc.
FOR FURTHER INFORMATION CONTACT: Questions regarding information,
registration, access or services for individuals with disabilities, or
logistics for the external peer-review meeting should be directed to
Stephanie Sarraino, Versar, Inc., Springfield, VA 22151; telephone:
703-750-3000 ext. 316; facsimile: 703-642-6954; e-mail
ssarraino@versar.com. To request accommodation of a disability, please
contact Versar, Inc. preferably at least 10 days prior to the meeting,
to give as much time as possible to process your request.
If you need technical information about the document, please
contact John Stanek, National Center for Environmental Assessment
(NCEA); telephone: 919-541-1048; facsimile: 919-541-0245; e-mail:
stanek.john@epa.gov.
SUPPLEMENTARY INFORMATION:
I. Summary of Information About the Project/Document
The draft Toxicological Review of Propionaldehyde is a new
assessment and provides scientific information on the effects
pertaining to exposure to propionaldehyde. Propionaldehyde was
nominated by the EPA Office of Air and Radiation in 2000 and 2001 and
by the Office of Air Quality Planning and Standards in 2003 as a
chemical listed for monitoring under the Clean Air Act. Propionaldehyde
is a colorless liquid with a suffocating, fruity odor. It is used in
the manufacturing of propionic acid and polyvinyl and other plastics,
in the synthesis of rubber chemicals, and as a disinfectant and
preservative. The chemical is released to the environment primarily
through the combustion of wood, gasoline, diesel fuel, and
polyethylene. Propionaldehyde is also a component of cigarette smoke
and a food additive/flavoring agent. Although no studies on the effects
of propionaldehyde administered by the oral route have been performed,
based on its expected daily intake (below 1800 ug/day) and eventual
metabolism in the citric acid cycle, it does not appear to be a safety
concern for public health via ingestion. Thus, the most probable route
[[Page 24282]]
of exposure of concern to the general population is by inhalation. The
assessment will present reference values for the noncancer effects of
propionaldehyde (RfD and RfC), where supported by available data, and a
cancer assessment.
II. Meeting Information
Members of the public may attend the meeting as observers, and
there will be a limited time for comments from the public. Please let
Versar, Inc. know if you wish to make comments during the meeting.
Space is limited, and reservations will be accepted on a first-come,
first-served basis.
Dated: April 24, 2008.
Rebecca Clark,
Director, National Center for Environmental Assessment.
[FR Doc. E8-9734 Filed 5-1-08; 8:45 am]
BILLING CODE 6560-50-P