SDS

Assessmen
t Mutagenicity
Imidacloprid was not mutagenic or genotoxic based on the overall weight of evidence in a battery of in
vitro and in vivo tests.
Ass
essment Carcinogenicity
Imidacloprid was not carcinogenic in lifetime feeding studies in rats and mice.
ACGIH
None.
NTP
None.
IARC
None.
OSHA
None.
Assessment toxicity to reproduction
Imidacloprid caused reproduction toxicity in a two-ge
neration stud
y in rats only at dose levels also toxic
to the parent animals. The reproduction toxicity seen with Imidacloprid is related to parental toxicity.
Assessment developmental toxicity
Imidacloprid caused developmental toxicity only at dose level
s toxic to the dam
s. The developmental
effects seen with Imidacloprid are related to maternal toxicity.
Further information
Acute toxicity studies have been bridge
d from a simila
r formulation(s).
The non-acute information pertains to the active ingredient(s).
SECTION 12: ECOLOGICAL INFORMATION
Toxicity to fish
LC50 (Oncorhynchus mykiss (rainbow trout)) 211 mg/l
Exposure time: 96 h
The value mentioned relates to the active ingredient imidacloprid.
Toxicity to aquatic
in
vertebra
tes
EC50 (Water flea (Daphnia magna)) 85 mg/l
Exposure time: 48 h
The value mentioned relates to the active ingredient imidacloprid.
LC50 (Chironomus
riparius (non-biting midge)) 0.0552 mg/l
Exposure time: 24 h
The value mentioned relates to the active ingredient imidacloprid.
Toxicity to aquatic plants
EC50
(Desmodesmus subspicatus) > 10 mg/l
SBM LIFE SCIENCE CORP.
SAFETY DATA SHEET
BIOADVANCED SCIENCE-BASED
SOLUTIONS FRUIT, CITRUS & VEGETABLE
INSECT CONTROL CONCENTRATE
7/10
Revision Date: 1/22/2019
Version 1.0 / USA
102000021168