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Edwards TCU 40/80 - Page 72

Edwards TCU 40/80
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TOXICOLOGICAL
INFORMATION
(Continued)
to
50,000
ppm.
HFC-126
does
not
produce
genetic
damage
in
bacterial
or
mammalian
call
cultures
or
when
tested
in
animals.
HFC-134a
Inhalation
4-hour
LC50:
567,000
ppm
in rats
A
5
or
10
second
spray
of
vapor
produced
very
slight
eye
irritation
and
a
24-hour
occlusive
application
produced
slight
skin
irritation
in
rabbits.
The
compound
is
not
a
skin
sensitizer
in
animals.
No
toxic
effects
were
seen
in
animals
from
exposures
by
inhalation
to
concentrations
up
to
81,000
ppm.
Lethargy
and
rapid
respiration
were
observed
at
a
vapor
concentration
of
305,000
ppm
and
pulmonary
congestion,
edema,
and
central
nervous
system
effects
occurred
at
a
vapor
concentration
of
750,000
ppm.
Cardiac
sensitization
occurred
in
dogs
at
75,000
ppm
following
an
epinephrine
challenge.
No
effects
in
animals
occurred
from
repeated
inhalation-exposures
to
99,000
ppm
for
two
weeks
or
higher
concentrations
to
50,000
ppm
for
three
months.
Repeated
exposures
to
higher
concentrations
caused
transient
tremors,
incoondination
and
some
organ
weight
changes.
Long-term
exposures
produced
increased
testes
weights
and
increased
urinary
fluoride
levels.
No
adverse
effects
were
observed
in
male
and
female
rats
fed
diets
containing
300
mg/kg/day
of
HFC-134a
for
52
weeks.
Animal
testing
indicates
that
this
compound
does
not
have
carcinogenic
or
mutagenic
effects.
Inhalation
of
50
000
ppm
for
two
years
caused
an
increase
in
benign
testicular
tumors
in
male
rats.
No
effects
were
observed
at
lower
concentrations.
The
tumors
were
late-occurring
and
were
judged
not
to
be
life-threatening.
Embryotoxic
activity
has
been
observed
in
some
animal
tests
but
only
at
high
concentrations
that
were
also
maternally
toxic.
HFC-143a
Inhalation
4-hour
LC50:
>540,000
ppm
in rats
Single
exposures
by
inhalation
to
500,000
ppm
caused
anesthesia
but
no
mortality
at
540,000
ppm.
Cardiac
sensitization
occurred
in
dogs
at
600,000
ppm
following
an
intravenous
challenge
with
epinephrine.
Two,
4-week
inhalation
have
been
conducted.
In the
first
study,
pathological
changes
in
the
testes
were
observed
at
all
exposure
concentrations;
no
effects
were
observed
in
females.
The
testicular
effect
was
considered
related
to
the
method
used
to
expose
the
rats
to
HFC-143a.
In
the
second
study using
the
same
exposure
concentrations,
no
effects
were
noted
in
males
at
any
concentration.
Data from
a
90-day
study
revealed
no
effects
in
male
or
female
rats
at
exposures
up
to
40,000
ppm.
Long-term
exposure
caused
significantly
decreased
body
weights
in
male
rats
fed
300
(continued)
66
TCU
40/80 Temperature
Control
Unit

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