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Notice of Filing a Pesticide Petition to Establish a Tolerance for a Certain Pesticide Chemical in or on Food

Note: EPA no longer updates this information, but it may be useful as a reference or resource.


 [Federal Register: September 27, 2000 (Volume 65, Number 188)]
[Notices]
[Page 58078-58080]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr27se00-79]

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ENVIRONMENTAL PROTECTION AGENCY

[PF-972; FRL-6742-4]


Notice of Filing a Pesticide Petition to Establish a Tolerance
for a Certain Pesticide Chemical in or on Food

AGENCY: Environmental Protection Agency (EPA).

ACTION: Notice.

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SUMMARY: This notice announces the initial filing of a pesticide
petition proposing the establishment of regulations for residues of a
certain pesticide chemical in or on various food commodities.

DATES: Comments, identified by docket control number PF-972, must be
received on or before October 27, 2000.

ADDRESSES: Comments may be submitted by mail, electronically, or in
person. Please follow the detailed instructions for each method as
provided in Unit I.C. of the SUPPLEMENTARY INFORMATION. To ensure
proper receipt by EPA, it is imperative that you identify docket
control number PF-972 in the subject line on the first page of your
response.

FOR FURTHER INFORMATION CONTACT: By mail: Bipin Gandhi, Registration
Division (7505C), Office of Pesticide Programs, Environmental
Protection Agency, 1200 Pennsylvania Ave., NW., Washington, DC 20460;
telephone number: (703) 308-8380; e-mail address: gandhi.bipin@epa.gov.

SUPPLEMENTARY INFORMATION:

I. General Information

A. Does this Action Apply to Me?

    You may be affected by this action if you are an agricultural
producer, food manufacturer or pesticide manufacturer. Potentially
affected categories and entities may include, but are not limited to:

------------------------------------------------------------------------
                                                          Examples of
           Categories                    NAICS            potentially
                                                      affected  entities
------------------------------------------------------------------------
Industry                          111                 Crop production
                                  112                 Animal production
                                  311                 Food manufacturing
                                  32532               Pesticide
                                                       manufacturing
------------------------------------------------------------------------

    This listing is not intended to be exhaustive, but rather provides
a guide for readers regarding entities likely to be affected by this
action. Other types of entities not listed in the table could also be
affected. The North American Industrial Classification System (NAICS)
codes have been provided to assist you and others in determining
whether or not this action might apply to certain entities. If you have
questions regarding the applicability of this action to a particular
entity, consult the person listed under FOR FURTHER INFORMATION
CONTACT.

B. How Can I Get Additional Information, Including Copies of this
Document and Other Related Documents?

    1. Electronically. You may obtain electronic copies of this
document, and certain other related documents that might be available
electronically, from the EPA Internet Home Page at http://www.epa.gov/.
To access this document, on the Home Page select ``Laws and
Regulations,'' ``Regulations and Proposed Rules,'' and then look up the
entry for this document under the ``Federal Register--Environmental
Documents.'' You can also go directly to the Federal Register listings
at http://www.epa.gov/fedrgstr/.
    2. In person. The Agency has established an official record for
this action under docket control number PF-972. The official record
consists of the documents specifically referenced in this action, any
public comments received during an applicable comment period, and other
information related to this action, including any information claimed
as confidential business information (CBI). This official record

[[Page 58079]]

includes the documents that are physically located in the docket, as
well as the documents that are referenced in those documents. The
public version of the official record does not include any information
claimed as CBI. The public version of the official record, which
includes printed, paper versions of any electronic comments submitted
during an applicable comment period, is available for inspection in the
Public Information and Records Integrity Branch (PIRIB), Rm. 119,
Crystal Mall #2, 1921 Jefferson Davis Highway, Arlington, VA, from 8:30
a.m. to 4 p.m., Monday through Friday, excluding legal holidays. The
PIRIB telephone number is (703) 305-5805.

C. How and to Whom Do I Submit Comments?

    You may submit comments through the mail, in person, or
electronically. To ensure proper receipt by EPA, it is imperative that
you identify docket control number PF-972 in the subject line on the
first page of your response.
    1. By mail. Submit your comments to: Public Information and Records
Integrity Branch (PIRIB), Information Resources and Services Division
(7502C), Office of Pesticide Programs (OPP), Environmental Protection
Agency, 1200 Pennsylvania Ave., NW., Washington, DC 20460.
    2. In person or by courier. Deliver your comments to: Public
Information and Records Integrity Branch (PIRIB), Information Resources
and Services Division (7502C), Office of Pesticide Programs (OPP),
Environmental Protection Agency, Rm. 119, Crystal Mall #2, 1921
Jefferson Davis Highway, Arlington, VA. The PIRIB is open from 8:30
a.m. to 4 p.m., Monday through Friday, excluding legal holidays. The
PIRIB telephone number is (703) 305-5805.
    3. Electronically. You may submit your comments electronically by
e-mail to: opp-docket@epa.gov, or you can submit a computer disk as
described above. Do not submit any information electronically that you
consider to be CBI. Avoid the use of special characters and any form of
encryption. Electronic submissions will be accepted in Wordperfect 6.1/
8.0 or ASCII file format. All comments in electronic form must be
identified by docket control number PF-972. Electronic comments may
also be filed online at many Federal Depository Libraries.

D. How Should I Handle CBI That I Want to Submit to the Agency?

    Do not submit any information electronically that you consider to
be CBI. You may claim information that you submit to EPA in response to
this document as CBI by marking any part or all of that information as
CBI. Information so marked will not be disclosed except in accordance
with procedures set forth in 40 CFR part 2. In addition to one complete
version of the comment that includes any information claimed as CBI, a
copy of the comment that does not contain the information claimed as
CBI must be submitted for inclusion in the public version of the
official record. Information not marked confidential will be included
in the public version of the official record without prior notice. If
you have any questions about CBI or the procedures for claiming CBI,
please consult the person identified under FOR FURTHER INFORMATION
CONTACT.

E. What Should I Consider as I Prepare My Comments for EPA?

    You may find the following suggestions helpful for preparing your
comments:
    1. Explain your views as clearly as possible.
    2. Describe any assumptions that you used.
    3. Provide copies of any technical information and/or data you used
that support your views.
    4. If you estimate potential burden or costs, explain how you
arrived at the estimate that you provide.
    5. Provide specific examples to illustrate your concerns.
    6. Make sure to submit your comments by the deadline in this
notice.
    7. To ensure proper receipt by EPA, be sure to identify the docket
control number assigned to this action in the subject line on the first
page of your response. You may also provide the name, date, and Federal
Register citation.

II. What Action is the Agency Taking?

    EPA has received a pesticide petition as follows proposing the
establishment and/or amendment of regulations for residues of a certain
pesticide chemical in or on various food commodities under section 408
of the Federal Food, Drug, and Comestic Act (FFDCA), 21 U.S.C. 346a.
EPA has determined that this petition contains data or information
regarding the elements set forth in section 408(d)(2); however, EPA has
not fully evaluated the sufficiency of the submitted data at this time
or whether the data support granting of the petition. Additional data
may be needed before EPA rules on the petition.

List of Subjects

    Environmental protection, Agricultural commodities, Feed additives,
Food additives, Pesticides and pests, Reporting and recordkeeping
requirements.

    Dated: September 15, 2000.
  James Jones,
Director, Registration Division, Office of Pesticide Programs.

Summary of Petition

    The petitioner summary of the pesticide petition is printed below
as required by section 408(d)(3) of the Federal Food Drug and Cosmetic
Act (FFDCA). The summary of the petition was prepared by the petitioner
and represents the view of the petitioner. EPA is publishing the
petition summary verbatim without editing it in any way. The petition
summary announce the availability of a description of the analytical
methods available to EPA for the detection and measurement of the
pesticide chemical residues or an explanation of why no such method is
needed.

DuPont Company

PP 6E4785

    EPA has received a pesticide petition (PP 6E4785) from the DuPont
Company, DuPont Fluoroproducts, Chestnut Run Plaza, P.O. Box 80711,
Wilmington, DE, 19880-0711 proposing, pursuant to section 408(d) of the
(FFDCA), 21 U.S.C. 346a(d), to amend 40 CFR part 180 by establishing a
tolerance for residues of dimethylether (CAS Reg. No. 115-10-6) when
used as an inert ingredient in pesticide formulations applied to
growing crops or to raw agricultural commodities (RAC) after harvest,
and including area application in and around commercial and residential
food handling facilities and establishments by certified applicators
only. EPA has determined that the petition contains data or information
regarding the elements set forth in section 408(d)(2) of the FFDCA;
however, EPA has not fully evaluated the sufficiency of the submitted
data at this time or whether the data support granting of the petition.
Additional data may be needed before EPA rules on the petition.

A. Residue Chemistry

    Analytical method. DME is used as a propellant in pesticide
formulations and exists as a gas at ambient conditions. Upon release
from the container, it vaporizes completely with essentially no
residue; consequently, no analytical method for residue measurement is
needed.

[[Page 58080]]

B. Toxicological Profile

    Since dimethylether (DME) exists as a gas at room temperature and
any exposure to humans would occur via inhalation, all toxicity testing
conducted with DME was done via inhalation or in the vapor phase.
    1. Acute toxicity. An acute inhalation toxicity study was conducted
in rats. The 4-hr LC50 was determined to be 164,000 parts
per million (ppm), EPA category IV.
    2. Genotoxicty--i. An in vitro Ames/Salmonella mutagenicity assay
in five commonly used strains was negative for mutagenic potential.
    ii. An in vitro chromosomal aberration test in cultured human
lymphocytes was negative for chromosomal aberrations.
    3. Reproductive and developmental toxicity--i. Reproductive organs
in male and female rats were examined histopathologically following
inhalation of 0, 2,000, 10,000, or 25,000 ppm DME for 6, 12, 16, and 24
months. The no observed adverse effect level (NOAEL) in this study was
25,000 ppm as no compound-related effects on the reproductive organs of
either male or female rats were observed.
    ii. Developmental toxicity testing was conducted in rats exposed
via inhalation to DME during days 6-15 of gestation. Fetal body weight
(bwt) was decreased at the 20,000 and 40,000 ppm levels (of borderline
statistical significance in the 20,000 ppm group) and there was an
increased incidence of several skeletal variations (partial rib
development in the lumbar region and partial or complete doubling of
one or more vertebral centra). The NOAEL for the conceptus was 1,250
ppm. In comparison to maternal effect levels, DME was not demonstrated
to represent a unique hazard to the rat conceptus.
    4. Subchronic toxicity. Male and female Wistar rats were exposed to
0, 200, 2,000, or 20,000 ppm DME via inhalation for 30 weeks. At the
20,000 ppm level, male rats showed a significant reduction in liver
weight accompanied by raised serum glutamic pyruvic transaminase (SGPT)
levels. In the 20,000 ppm females, there was no significant effect on
liver weight but SGPT levels were raised. The NOAEL in this study was
2,000 ppm.
    5. Chronic toxicity. A 2-year DME inhalation study was conducted in
rats for 6 hours/day, 5 days/week at concentrations of 0, 2,000,
10,000, or 25,000 ppm. The NOAEL was 2,000 ppm based on an increase in
bwt and a decrease in survival in male rats exposed to 10,000 or 25,000
ppm DME vapors and on hemolytic effects noted in male rats exposed to
25,000 ppm DME vapors for 6 months. No neoplastic lesions were observed
that could be attributable to DME exposure. DME was not carcinogenic.
    6. Animal metabolism. Dimethylether is a volatile, stable compound.
While no metabolism studies were identified, the primary route of DME
elimination from the body is likely to be exhalation of parent
compound.
    7. Endocrine disruption. No adverse endocrine effects have been
suggested or reported in any toxicity tests conducted with DME.

C. Aggregate Exposure

    1. Dietary exposure. Dimethylether exists as a vapor at atmospheric
pressure and ambient temperatures. It is handled and contained in
aerosol products as a liquefied gas under its own vapor pressure which
is 63 psig at 70 deg.F. Upon release from container pressure, as when
product is dispensed, dimethylether vaporizes completely with
essentially no residue. Dimethylether is intended as an inert
ingredient and propellant for pesticide formulations applied in food
handling areas and establishments; these products are not intended for
direct application to foods. Dietary exposure from use of dimethylether
in these types of products is believed to be minimal, as discussed in
food and drinking water below.
    i. Food. Based on its physical properties, when dimethylether is
used as a propellant in pesticide formulations applied in food handling
areas and establishments, no residue is expected on or in food. Upon
dispensing the insect control product, the dimethylether will vaporize
and dissipate quickly, affording no residue or accumulation.
    ii. Drinking water. Similarly, since dimethylether will vaporize
completely at ambient conditions, no accumulation is expected in
drinking water. There would be no liquid dimethylether to migrate to
groundwater aquifers or surface water bodies that may serve as suitable
drinking water sources.
    2. Non-dietary exposure. The greatest potential for residential
exposure to dimethylether would be via inhalation routes. However, even
when these pesticide products are used in small areas, estimated
dimethylether levels will be lower and of much shorter duration than
recognized and accepted levels that are considered safe for chronic
lifetime exposures. Additionally, tests have shown that such aerosol
propellants dissipate within minutes of use.

D. Cumulative Effects

    There is no reliable information that would indicate or suggest
that dimethylether has any toxic effect on mammals that would be
cumulative with those of any other chemical.

E. Safety Determination

    1. U.S. population. Since potential dietary exposures are expected
to be minimal, if any, and since potential inhalation exposures are
estimated much lower than recognized and accepted levels considered
safe for chronic lifetime exposures, dimethylether is not likely to
pose any significant risk to the general U.S. population.
    2. Infants and children. To the best of our knowledge, there is no
information that suggests infants and children are more susceptible to
exposure to or effects of dimethylether. The lack of significant
toxicity in reproductive/developmental studies on dimethylether
suggests that growing organisms are not at increased risks. Since
potential dietary exposures to infants and children are minimal, if
any, based on anticipated use, it is unlikely that any significant
risks exist. Direct exposures to infants and children via inhalation
are not anticipated for the intended use of dimethylether.

F. International Tolerances

    DuPont is not aware of any tolerances for dimethylether outside the
United States.
[FR Doc. 00-24438 Filed 9-26-00; 8:45 am]
BILLING CODE 6560-50-S 

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