SDS

Exposure time: 1 h
Determined
in the form of liquid aerosol.
Extrapolated from the 4 hr LC50.
(actual)
Acute dermal toxicity
LD5
0 (rabbit) > 2,000 mg/k
g
Skin irritation
No skin irritation
Eye irritation
Moderate eye irritation.
Sensitisation
Non-sen
s
itizing. (guinea pig)
Assessment repeated dose toxicity
Triclopyr did not cause specific target organ toxicity in experim
ental animal stud
ies.
Assessment mutagenicity
Triclopyr was not mutagenic or genotoxic in a battery
of in vitro and in vivo tests.
Assessme
nt carcinogenicity
Triclopyr was not carcinogenic in lifetime feeding studies in rats and mice.
ACGIH
None.
NTP
None.
IARC
None.
OSHA
None.
Assessment toxicity to reproduction
Triclopyr did not cause reproductive toxicity in a two-g
eneration study in rats.
Ass
essment developmental toxicity
Triclopyr caused developmental toxicity only at dose levels toxic
to the dams. The develop
mental effects
seen with Triclopyr are related to maternal toxicity.
Further information
Acute toxicity studies have been bridge
d from a similar formulatio
n(s).
The non-acute information pertains to the active ingredient(s).
SECTION 12: ECOLOGICAL INFORMATION
Biodegradability
Triclopyr:
not rapidly biodegradable
SBM LIFE SCIENCE CORP.
SAFETY DATA SHEET
BIOADVANCED SCIENCE-BASED
SOLUTIONS BRUSH KILLER PLUS READY-
TO-USE
Version 1.0 / USA
102000013153
6/9
Revision Date: 01/22/2019