[Federal Register Volume 81, Number 157 (Monday, August 15, 2016)]
[Rules and Regulations]
[Pages 53931-53935]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-19115]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 180
[EPA-HQ-OPP-2015-0719; FRL-9949-49]
n-Butyl 3-hydroxybutyrate and Isopropyl 3-hydroxybutyrate;
Exemption From the Requirement of a Tolerance
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This regulation establishes exemptions from the requirement of
a tolerance for residues of n-butyl 3-hydroxybutyrate (CAS Reg. No.
53605-94-0) and isopropyl 3-hydroxybutyrate (CAS Reg. No. 54074-94-1)
when used as inert ingredients (solvents) in pesticide formulations
applied to growing crops or raw agricultural commodities after harvest;
to animals; and to food contact surfaces in public eating places,
dairy-processing equipment, and food-processing equipment and utensils.
Steptoe and Johnson, on behalf of Eastman Chemical Company, submitted a
petition to EPA under the Federal Food, Drug, and Cosmetic Act (FFDCA),
requesting establishment of these exemptions from the requirement of a
tolerance. This regulation eliminates the need to establish a maximum
permissible level for residues of n-butyl 3-hydroxybutyrate and
isopropyl 3-hydroxybutyrate when applied or used under these
conditions.
DATES: This regulation is effective August 15, 2016. Objections and
requests for hearings must be received on or before October 14, 2016,
and must be filed in accordance with the instructions provided in 40
CFR part 178 (see also Unit I.C. of the SUPPLEMENTARY INFORMATION).
ADDRESSES: The docket for this action, identified by docket
identification (ID) number EPA-HQ-OPP-2015-0719, is available at http://www.regulations.gov or at the Office of Pesticide Programs Regulatory
Public Docket (OPP Docket) in the Environmental Protection Agency
Docket Center (EPA/DC), West William Jefferson Clinton Bldg., Rm. 3334,
1301 Constitution Ave. NW., Washington, DC 20460-0001. The Public
Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through
Friday, excluding legal holidays. The telephone number for the Public
Reading Room is (202) 566-1744, and the telephone number for the OPP
Docket is (703) 305-5805. Please review the visitor instructions and
additional information about the docket available at http://www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT: Susan Lewis, Registration Division
(7505P), Office of Pesticide Programs, Environmental Protection Agency,
1200 Pennsylvania Ave. NW., Washington, DC 20460-0001; main telephone
number: (703) 305-7090; email address: [email protected].
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
You may be potentially affected by this action if you are an
agricultural producer, food manufacturer, or pesticide manufacturer.
The following list of North American Industrial Classification System
(NAICS) codes is not intended to be exhaustive, but rather provides a
guide to help readers determine whether this document applies to them.
Potentially affected entities may include:
Crop production (NAICS code 111).
Animal production (NAICS code 112).
Food manufacturing (NAICS code 311).
Pesticide manufacturing (NAICS code 32532).
B. How can I get electronic access to other related information?
You may access a frequently updated electronic version of 40 CFR
part 180 through the Government Printing Office's e-CFR site at http://www.ecfr.gov/cgi-bin/text-idx?&c=ecfr&tpl=/ecfrbrowse/Title40/40tab_02.tpl.
C. How can I file an objection or hearing request?
Under FFDCA section 408(g), 21 U.S.C. 346a, any person may file an
objection to any aspect of this regulation and may also request a
hearing on those objections. You must file your objection or request a
hearing on this regulation in accordance with the instructions provided
in 40 CFR part 178. To ensure proper receipt by EPA, you must identify
docket ID number EPA-HQ-OPP-2015-0719 in the subject line on the first
page of your submission. All objections and requests for a hearing must
be in writing, and must be received by the Hearing Clerk on or before
October 14, 2016. Addresses for mail and hand delivery of objections
and hearing requests are provided in 40 CFR 178.25(b).
In addition to filing an objection or hearing request with the
Hearing Clerk as described in 40 CFR part 178, please submit a copy of
the filing (excluding any Confidential Business Information (CBI)) for
inclusion in the public docket. Information not marked confidential
pursuant to 40 CFR part 2 may be disclosed publicly by EPA without
prior notice. Submit the non-CBI copy of your objection or hearing
request, identified by docket ID number EPA-HQ-OPP-2015-0719, by one of
the following methods:
Federal eRulemaking Portal: http://www.regulations.gov.
Follow the online instructions for submitting comments. Do not submit
electronically any information you consider to be CBI or other
information whose disclosure is restricted by statute.
Mail: OPP Docket, Environmental Protection Agency Docket
Center (EPA/DC), (28221T), 1200 Pennsylvania Ave. NW., Washington, DC
20460-0001.
Hand Delivery: To make special arrangements for hand
delivery or delivery of boxed information, please follow the
instructions at http://www.epa.gov/dockets/contacts.html. Additional
instructions on commenting or visiting the docket, along with more
information about dockets generally, is available at http://www.epa.gov/dockets.
II. Petition for Exemption
In the Federal Register of November 23, 2015 (80 FR 72941) (FRL-
9936-73), EPA issued a document pursuant to FFDCA section 408, 21
U.S.C. 346a, announcing the filing of a pesticide petition (PP IN-
10841) by Steptoe and Johnson LLP (1330 Connecticut Avenue NW.,
Washington, DC 20036-1795) on behalf of the Eastman Chemical Company
(200 South Wilcox Drive, Kingsport, TN 37660-5280). The petition
requested that 40 CFR 180.910, 180.930, and 180.940 be amended to
establish exemptions from the requirement of a tolerance for residues
of n-butyl 3-hydroxybutyrate (CAS Reg. No. 53605-94-0); and isopropyl
3-hydroxybutyrate (CAS Reg. No. 54074-94-1) when used as inert
ingredients (solvents) in pesticide formulations applied to pre- and
post-harvest crops under 40 CFR 180.910; to animals under 40 CFR
180.930; and to food contact surface sanitizing solutions under 40 CFR
180.940(a). That document referenced a summary of the petition prepared
by Steptoe and Johnson on behalf of Eastman Chemical Company, the
petitioner, which is available in the docket, http://www.regulations.gov.
[[Page 53932]]
Comments were received on the notice of filing. EPA's response to these
comments is discussed in Unit V.B.
III. Inert Ingredient Definition
Inert ingredients are all ingredients that are not active
ingredients as defined in 40 CFR 153.125 and include, but are not
limited to, the following types of ingredients (except when they have a
pesticidal efficacy of their own): Solvents such as alcohols and
hydrocarbons; surfactants such as polyoxyethylene polymers and fatty
acids; carriers such as clay and diatomaceous earth; thickeners such as
carrageenan and modified cellulose; wetting, spreading, and dispersing
agents; propellants in aerosol dispensers; microencapsulating agents;
and emulsifiers. The term ``inert'' is not intended to imply
nontoxicity; the ingredient may or may not be chemically active.
Generally, EPA has exempted inert ingredients from the requirement of a
tolerance based on the low toxicity of the individual inert
ingredients.
IV. Aggregate Risk Assessment and Determination of Safety
Section 408(c)(2)(A)(i) of FFDCA allows EPA to establish an
exemption from the requirement for a tolerance (the legal limit for a
pesticide chemical residue in or on a food) only if EPA determines that
the tolerance is ``safe.'' Section 408(b)(2)(A)(ii) of FFDCA defines
``safe'' to mean that ``there is a reasonable certainty that no harm
will result from aggregate exposure to the pesticide chemical residue,
including all anticipated dietary exposures and all other exposures for
which there is reliable information.'' This includes exposure through
drinking water and in residential settings, but does not include
occupational exposure. Section 408(b)(2)(C) of FFDCA requires EPA to
give special consideration to exposure of infants and children to the
pesticide chemical residue in establishing a tolerance and to ``ensure
that there is a reasonable certainty that no harm will result to
infants and children from aggregate exposure to the pesticide chemical
residue. . . .''
EPA establishes exemptions from the requirement of a tolerance only
in those cases where it can be clearly demonstrated that the risks from
aggregate exposure to pesticide chemical residues under reasonably
foreseeable circumstances will pose no appreciable risks to human
health. In order to determine the risks from aggregate exposure to
pesticide inert ingredients, the Agency considers the toxicity of the
inert in conjunction with possible exposure to residues of the inert
ingredient through food, drinking water, and through other exposures
that occur as a result of pesticide use in residential settings. If EPA
is able to determine that a finite tolerance is not necessary to ensure
that there is a reasonable certainty that no harm will result from
aggregate exposure to the inert ingredient, an exemption from the
requirement of a tolerance may be established.
Consistent with FFDCA section 408(c)(2)(A), and the factors
specified in FFDCA section 408(c)(2)(B), EPA has reviewed the available
scientific data and other relevant information in support of this
action. EPA has sufficient data to assess the hazards of and to make a
determination on aggregate exposure for n-butyl 3-hydroxybutyrate and
isopropyl 3-hydroxybutyrate including exposure resulting from the
exemption established by this action. EPA's assessment of exposures and
risks associated with n-butyl 3-hydroxybutyrate and isopropyl 3-
hydroxybutyrate follows.
A. Toxicological Profile
EPA has evaluated the available toxicity data and considered their
validity, completeness, and reliability as well as the relationship of
the results of the studies to human risk. EPA has also considered
available information concerning the variability of the sensitivities
of major identifiable subgroups of consumers, including infants and
children. Specific information on the studies received and the nature
of the adverse effects caused by n-butyl 3-hydroxybutyrate and
isopropyl 3-hydroxybutyrate as well as the no-observed-adverse-effect-
level (NOAEL) and the lowest-observed-adverse-effect-level (LOAEL) from
the toxicity studies are discussed in this unit.
n-Butyl-3-hydroxybutyrate and isopropyl-3-hydroxybutyrate are
structurally similar chemical entities differing only in one methyl
group (CH3). Therefore the toxicity of these two chemicals
is expected to be similar. Since there are no adequate data available
for each one individually, the Agency utilizes read-across data to fill
data gaps.
n-Butyl-3-hydroxybutyrate and isopropyl-3-hydroxybutyrate both
exhibit very low levels of acute oral, dermal and inhalation toxicity
each with LD50 values >5,000 mg/kg. n-Butyl-3-
hydroxybutyrate is moderately irritating to the rabbit eye and is
slightly irritating to rabbit skin. Isopropyl-3-hydroxybutyrate is not
irritating to rabbit skin. n-Butyl-3-hydroxybutyrate and isopropyl-3-
hydroxybutyrate are not dermal sensitizers.
In a 28-day subchronic feeding study in rats which included a
reproduction/developmental screening assessment, exposure to isopropyl-
3-hydroxybutyrate resulted in no adverse test item-related
toxicological effects on clinical observations, no adverse effects seen
in FOB assessments, no adverse effects on motor activity evaluations,
no adverse effects seen in gross necropsy observations, male or female
reproductive performance, or neurobehavioral parameters. The no-
observed-adverse-effect-level (NOAEL) for reproductive toxicity was
1,000 mg/kg/day. The NOAEL for systemic toxicity was 1,000 mg/kg/day.
In the absence of effects on the general physical condition of
F1 pups, the NOAEL for neonatal toxicity was 1,000 mg/kg/
day.
n-Butyl-3-hydroxybutyrate and isopropyl-3-hydroxybutyrate were
negative in reverse gene mutation assays. Isopropyl-3-hydroxybutyrate
was negative in a chromosome aberration assay and a gene mutation
assay.
There were no neurotoxicity or immunotoxicity studies available.
However, there was no evidence of adverse neurotoxic effects noted
during the FOB evaluations and the motor activity evaluations. There
was no evidence of immunotoxicity in the available database.
Based on the negative responses seen in the genotoxicity and lack
of systemic toxicity in the reproductive and developmental screening
study, n-butyl-3-hydroxybutyrate and isopropyl-3-hydroxybutyrate are
considered unlikely to be carcinogenic.
n-Butyl-3-hydroxybutyrate and isopropyl-3-hydroxybutyrate both have
a low solubility; therefore, it is unlikely that either material will
be absorbed by the body and become systemically bioavailable. Both
compounds are expected to hydrolyze quickly and completely in vivo, and
the resulting hydrolysis products are very close in structure or are
the same, depending on the specific hydrolysis product. The available
in vitro data suggests that isopropyl-3-hydroxybutyrate can undergo
fast hydrolysis by enzymes in the plasma and liver to produce n-butyl-
3-hydroxybutyrate, which is perhaps further metabolized. Isopropyl-3-
hydroxybutyrate concentration decreased from approximately 70 [mu]M to
below the limit of detection (<6.68 [mu]M) in plasma within 2 hours and
in rat liver S9 fraction within 30 minutes. Although stable in
phosphate buffer, isopropyl-3-
[[Page 53933]]
hydroxybutyrate concentration levels decreased from 70 [mu]M to below
the LOD within 30 minutes with ONLY slight increases in beta-
hydroxybutyate levels indicating that either it is formed in small
quantity (minor pathway) and/or rapidly metabolized and removed from
the circulation.
B. Toxicological Points of Departure/Levels of Concern
Once a pesticide's toxicological profile is determined, EPA
identifies toxicological points of departure (POD) and levels of
concern to use in evaluating the risk posed by human exposure to the
pesticide. For hazards that have a threshold below which there is no
appreciable risk, the toxicological POD is used as the basis for
derivation of reference values for risk assessment. PODs are developed
based on a careful analysis of the doses in each toxicological study to
determine the dose at which no adverse effects are observed (the NOAEL)
and the lowest dose at which adverse effects of concern are identified
(the LOAEL). Uncertainty/safety factors are used in conjunction with
the POD to calculate a safe exposure level--generally referred to as a
population-adjusted dose (PAD) or a reference dose (RfD)--and a safe
margin of exposure (MOE). For non-threshold risks, the Agency assumes
that any amount of exposure will lead to some degree of risk. Thus, the
Agency estimates risk in terms of the probability of an occurrence of
the adverse effect expected in a lifetime. For more information on the
general principles EPA uses in risk characterization and a complete
description of the risk assessment process, see http://www.epa.gov/pesticides/factsheets/riskassess.htm.
An acute effect was not found in the database therefore an acute
dietary assessment is not necessary. In the 28-day subchronic oral
toxicity study in rats with neurotoxicity measurements, no toxicity was
observed at doses up to 1,000 mg/kg/day. Therefore, the Agency
concluded that it is not necessary to conduct a quantitative risk
assessment.
C. Exposure Assessment
1. Dietary exposure from food, feed uses and drinking water. In
evaluating dietary exposure to n-butyl-3-hydroxybutyrate and isopropyl-
3-hydroxybutyrate, EPA considered exposure under the proposed exemption
from the requirement of a tolerance. EPA assessed dietary exposures
from n-butyl-3-hydroxybutyrate and isopropyl-3-hydroxybutyrate in food
and drinking water as follows: Dietary exposure can occur from eating
foods or ingesting drinking water containing residues of n-butyl-3-
hydroxybutyrate and isopropyl-3-hydroxybutyrate. Because no hazard
endpoint of concern was identified for the acute and chronic dietary
assessment (food, feed and drinking water uses, a quantitative dietary
exposure risk assessment was not conducted
2. From non-dietary exposure. The term ``residential exposure'' is
used in this document to refer to non-occupational, non-dietary
exposure (e.g., textiles (clothing and diapers), carpets, swimming
pools, and hard surface disinfection on walls, floors, tables).
n-Butyl-3-hydroxybutyrate and isopropyl-3-hydroxybutyrate may be
used in inert ingredients in products that are registered for specific
uses that may result in residential exposure, such as pesticides used
in and round the home. However, since no endpoint of concern identified
in the available database, it is not necessary to conduct a
quantitative residential exposure assessment.
3. Cumulative effects from substances with a common mechanism of
toxicity. Section 408(b)(2)(D)(v) of FFDCA requires that, when
considering whether to establish, modify, or revoke a tolerance, the
Agency consider ``available information'' concerning the cumulative
effects of a particular pesticide's residues and ``other substances
that have a common mechanism of toxicity.''
EPA has not found n-butyl-3-hydroxybutyrate and isopropyl-3-
hydroxybutyrate to share a common mechanism of toxicity with any other
substances, and n-butyl-3-hydroxybutyrate and isopropyl-3-
hydroxybutyrate does not appear to produce a toxic metabolite produced
by other substances. For the purposes of this tolerance action,
therefore, EPA has assumed that n-butyl-3-hydroxybutyrate and
isopropyl-3-hydroxybutyrate does not have a common mechanism of
toxicity with other substances. For information regarding EPA's efforts
to determine which chemicals have a common mechanism of toxicity and to
evaluate the cumulative effects of such chemicals, see EPA's Web site
at http://www.epa.gov/pesticides/cumulative.
D. Safety Factor for Infants and Children
1. In general. Section 408(b)(2)(C) of FFDCA provides that EPA
shall apply an additional tenfold (10X) margin of safety for infants
and children in the case of threshold effects to account for prenatal
and postnatal toxicity and the completeness of the database on toxicity
and exposure unless EPA determines based on reliable data that a
different margin of safety will be safe for infants and children. This
additional margin of safety is commonly referred to as the FQPA Safety
Factor (SF). In applying this provision, EPA either retains the default
value of 10X, or uses a different additional safety factor when
reliable data available to EPA support the choice of a different
factor.
As part of its qualitative assessment, EPA evaluated the available
toxicity and exposure data on n-butyl-3-hydroxybutyrate and isopropyl-
3-hydroxybutyrate and considered its validity, completeness, and
reliability, as well as the relationship of this information to human
risk. EPA considers the toxicity database to be sufficient to evaluate
risk and has identified no residual uncertainty with regard to prenatal
and postnatal toxicity or exposure. No hazard was identified based on
the available studies; therefore, EPA concludes that there are no
threshold effects of concern to infants, children, or adults from n-
butyl-3-hydroxybutyrate and isopropyl-3-hydroxybutyrate. As a result,
EPA concludes that no additional margin of exposure (safety) is
necessary.
E. Aggregate Risks and Determination of Safety
Because no toxicological endpoints of concern were identified, EPA
concludes that aggregate exposure to residues of n-butyl-3-
hydroxybutyrate and isopropyl-3-hydroxybutyrate will not pose a risk to
the U.S. population, including infants and children, and that there is
a reasonable certainty that no harm will result to the general
population, or to infants and children from aggregate exposure to n-
butyl-3-hydroxybutyrate and isopropyl-3-hydroxybutyrate residues.
V. Other Considerations
A. Analytical Enforcement Methodology
An analytical method is not required for enforcement purposes since
the Agency is not establishing a numerical tolerance for residues of n-
butyl-3-hydroxybutyrate and isopropyl-3-hydroxybutyrate in or on any
food commodities. EPA is not establishing a limitation on the amount of
n-butyl-3-hydroxybutyrate and isopropyl-3-hydroxybutyrate that may be
used in pesticide formulations applied to growing crops.
B. Comments
Two generic comments objecting to the use of chemicals in food were
submitted to the docket for this action.
[[Page 53934]]
Neither of the comments contained any specific information bearing on
the Agency's safety finding for these chemicals. The Agency understands
the commenters' concerns and recognizes that some individuals believe
that pesticides should be banned on agricultural crops. However, the
existing legal framework provided by section 408 of the Federal Food,
Drug and Cosmetic Act (FFDCA) states that tolerances may be set when
persons seeking such tolerances or exemptions have demonstrated that
the pesticide meets the safety standard imposed by that statute. The
comment appears to be directed at the underlying statute and not EPA's
implementation of it; the citizen has made no contention that EPA has
acted in violation of the statutory framework.
VI. Conclusions
Therefore, exemptions from the requirement of a tolerance are
established under 40 CFR 180.910, 40 CFR 180.930, and 40 CFR 180.940(a)
for n-butyl-3-hydroxybutyrate (CAS Reg. No. 53605-94-0) and isopropyl-
3-hydroxybutyrate (CAS Reg. No. 54074-94-1) when used as inert
ingredients (solvents) in pesticide formulations applied to growing
crops or raw agricultural commodities after harvest (40 CFR 180.910);
to animals (40 CFR 180.930); or to food contact surfaces in public
eating places, dairy-processing equipment, and food-processing
equipment and utensils (40 CFR 180.940(a)).
VII. Statutory and Executive Order Reviews
This action establishes exemptions from the requirement of a
tolerance under FFDCA section 408(d) in response to a petition
submitted to the Agency. The Office of Management and Budget (OMB) has
exempted these types of actions from review under Executive Order
12866, entitled ``Regulatory Planning and Review'' (58 FR 51735,
October 4, 1993). Because this action has been exempted from review
under Executive Order 12866, this action is not subject to Executive
Order 13211, entitled ``Actions Concerning Regulations That
Significantly Affect Energy Supply, Distribution, or Use'' (66 FR
28355, May 22, 2001) or Executive Order 13045, entitled ``Protection of
Children from Environmental Health Risks and Safety Risks'' (62 FR
19885, April 23, 1997). This action does not contain any information
collections subject to OMB approval under the Paperwork Reduction Act
(PRA) (44 U.S.C. 3501 et seq.), nor does it require any special
considerations under Executive Order 12898, entitled ``Federal Actions
to Address Environmental Justice in Minority Populations and Low-Income
Populations'' (59 FR 7629, February 16, 1994).
Since tolerances and exemptions that are established on the basis
of a petition under FFDCA section 408(d), such as the exemptions in
this final rule, do not require the issuance of a proposed rule, the
requirements of the Regulatory Flexibility Act (RFA) (5 U.S.C. 601 et
seq.), do not apply.
This action directly regulates growers, food processors, food
handlers, and food retailers, not States or tribes, nor does this
action alter the relationships or distribution of power and
responsibilities established by Congress in the preemption provisions
of FFDCA section 408(n)(4). As such, the Agency has determined that
this action will not have a substantial direct effect on States or
tribal governments, on the relationship between the national government
and the States or tribal governments, or on the distribution of power
and responsibilities among the various levels of government or between
the Federal Government and Indian tribes. Thus, the Agency has
determined that Executive Order 13132, entitled ``Federalism'' (64 FR
43255, August 10, 1999) and Executive Order 13175, entitled
``Consultation and Coordination with Indian Tribal Governments'' (65 FR
67249, November 9, 2000) do not apply to this action. In addition, this
action does not impose any enforceable duty or contain any unfunded
mandate as described under Title II of the Unfunded Mandates Reform Act
(UMRA) (2 U.S.C. 1501 et seq.).
This action does not involve any technical standards that would
require Agency consideration of voluntary consensus standards pursuant
to section 12(d) of the National Technology Transfer and Advancement
Act (NTTAA) (15 U.S.C. 272 note).
VIII. Congressional Review Act
Pursuant to the Congressional Review Act (5 U.S.C. 801 et seq.),
EPA will submit a report containing this rule and other required
information to the U.S. Senate, the U.S. House of Representatives, and
the Comptroller General of the United States prior to publication of
the rule in the Federal Register. This action is not a ``major rule''
as defined by 5 U.S.C. 804(2).
List of Subjects in 40 CFR Part 180
Environmental protection, Administrative practice and procedure,
Agricultural commodities, Pesticides and pests, Reporting and
recordkeeping requirements.
Dated: July 25, 2016.
Daniel J. Rosenblatt,
Acting Director, Registration Division, Office of Pesticide Programs.
Therefore, 40 CFR chapter I is amended as follows:
PART 180--[AMENDED]
0
1. The authority citation for part 180 continues to read as follows:
Authority: 21 U.S.C. 321(q), 346a and 371.
0
2. In Sec. 180.910, add alphabetically the inert ingredients to the
table to read as follows:
Sec. 180.910 Inert ingredients used pre- and post-harvest; exemptions
from the requirement of a tolerance.
* * * * *
------------------------------------------------------------------------
Inert ingredients Limits Uses
------------------------------------------------------------------------
* * * * * * *
n-Butyl-3-hydroxybutyrate (CAS .............. Solvent.
Reg. No. 53605-94-0).
* * * * * * *
Isopropyl-3-hydroxybutyrate (CAS .............. Solvent.
Reg. No. 54074-94-1).
* * * * * * *
------------------------------------------------------------------------
[[Page 53935]]
0
3. In Sec. 180.930, add alphabetically the inert ingredients to the
table to read as follows:
Sec. 180.930 Inert ingredients applied to animals; exemptions from
the requirement of a tolerance.
* * * * *
------------------------------------------------------------------------
Inert ingredients Limits Uses
------------------------------------------------------------------------
* * * * * * *
n-Butyl-3-hydroxybutyrate (CAS .............. Solvent.
Reg. No. 53605-94-0).
* * * * * * *
Isopropyl-3-hydroxybutyrate (CAS .............. Solvent.
Reg. No. 54074-94-1).
* * * * * * *
------------------------------------------------------------------------
0
4. In Sec. 180.940(a), add alphabetically the inert ingredients to the
table in paragraph (a) to read as follows:
Sec. 180.940 Tolerance exemptions for active and inert ingredients
for use in antimicrobial formulations (Food-contact surface sanitizing
solutions).
* * * * *
(a) * * *
------------------------------------------------------------------------
Pesticide chemical CAS Reg. No. Limits
------------------------------------------------------------------------
* * * * * * *
n-Butyl-3-hydroxybutyrate......... 53605-94-0 Solvent.
* * * * * * *
Isopropyl-3-hydroxybutyrate....... 54074-94-1 Solvent.
* * * * * * *
------------------------------------------------------------------------
* * * * *
[FR Doc. 2016-19115 Filed 8-12-16; 8:45 am]
BILLING CODE 6560-50-P