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[ CAS No. 72748-35-7 ] {[proInfo.proName]}

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Type HazMat fee for 500 gram (Estimated)
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Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 72748-35-7
Chemical Structure| 72748-35-7
Structure of 72748-35-7 * Storage: {[proInfo.prStorage]}

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Product Citations

Product Citations

Mia?Arkles ; Federico?Sinche1 ; Michael?J.?Lydy DOI: PubMed ID:

Abstract: Tenax extraction, a measure of chemical desorption rates from sediments, was used to evaluate the bioaccessibility of bifenthrin in two different sediments exposed to three temperatures aged over a 56-d holding period. A 24-h single-point Tenax extraction was used and parent 14C-bifenthrin and polar metabolites were quantified in the sediment and Tenax. Bioaccessibility of bifenthrin was inversely related to the organic carbon (OC) content in the sediment, holding time, and temperature. Sequestration of the bifenthrin into slowly desorbing fractions within the sediment appears to have decreased degradation of the parent compound into metabolites and decreased the amount of parent compound bioaccessible for uptake by the Tenax. These results suggest that the environmental risk of bifenthrin to aquatic species is greatest immediately after the pesticide enters a waterbody after runoff, for low-OC content sediments, and in areas or seasons where water temperatures are colder.

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Product Details of [ 72748-35-7 ]

CAS No. :72748-35-7 MDL No. :MFCD04112623
Formula : C9H10ClF3O2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 242.62 Pubchem ID :-
Synonyms :

Calculated chemistry of [ 72748-35-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.67
Num. rotatable bonds : 3
Num. H-bond acceptors : 5.0
Num. H-bond donors : 1.0
Molar Refractivity : 49.29
TPSA : 37.3 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.39 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.42
Log Po/w (XLOGP3) : 3.36
Log Po/w (WLOGP) : 4.29
Log Po/w (MLOGP) : 2.51
Log Po/w (SILICOS-IT) : 2.6
Consensus Log Po/w : 2.84

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -3.26
Solubility : 0.132 mg/ml ; 0.000546 mol/l
Class : Soluble
Log S (Ali) : -3.82
Solubility : 0.0366 mg/ml ; 0.000151 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.99
Solubility : 2.51 mg/ml ; 0.0104 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.32

Safety of [ 72748-35-7 ]

Signal Word:Danger Class:8
Precautionary Statements:P501-P260-P270-P264-P280-P303+P361+P353-P301+P330+P331-P363-P301+P312+P330-P304+P340+P310-P305+P351+P338+P310-P405 UN#:1759
Hazard Statements:H302-H314 Packing Group:
GHS Pictogram:
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