SDS

Exposure time: 1 h
Determined in the form of liquid aero
sol.
Extrapolated from the 4 hr LC50.
(actual)
Acute dermal toxicity
LD5
0 (rabbit) > 2,000 mg/kg
Skin irritation
No skin irritation
Ey
e irritation
Moderate eye irritation.
Sensitisation
Non-sen
sitizing. (guin
ea pig)
Assessment repeated dose toxicity
Triclopyr did not cause specific target organ toxicity in experim
ental animal studies.
Assessme
nt mutagenicity
Triclopyr was not mutagenic or genotoxic in a battery
of in vitro and in vivo tests.
Assessment carcinogenicit
y
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.
Assessment dev
elopmental toxicity
Triclopyr caused developmental toxicity only at dose levels toxic
to the dams. The developmental effect
s
seen with Triclopyr are related to maternal toxicity.
Further information
Acute toxicity studies have been bridge
d from a similar formulation(s).
The non-a
cute 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 EXTENDED CONTROL
BRUSH KILLER READY-TO-USE
Version 1.0 / USA
6/9
Revision Date: 06/14/2021