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1031-07-8
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???(??):
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ENDOSULFAN SULFATE
???(??):
ENDOSULFAN-SULPHATE;THIODAN SULFATE;BENZOEPIN SULFATE;ENDOSULFAN SULFATE;hiepin-3,3-dioxide;Enoosulfan sulfate;ENDOSULPHANSULPHATE;xahydro-,3,3-dioxide;Endosulfan Impurity 1;endosulfancyclicsulfate
CBNumber:
CB4457785
???:
C9H6Cl6O4S
??? ??:
422.92
MOL ??:
1031-07-8.mol
MSDS ??:
SDS

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???
147.71°C
?? ?
480.7±45.0 °C(Predicted)
??
1.6835 (estimate)
???
9.75 x 10-6 mmHg at 25 °C (subcooled liquid vapor pressure calculated from GC retention time data,Hinckley et al., 1990)
???
-26 °C
?? ??
APPROX 4°C
???
DMSO: Slightly Soluble,Methanol: Slightly Soluble
??? ??
??
??
???
???
117ppb (Ali, 1978)
Henry's Law Constant
4.64(x 10-5 atmm3/mol) at 25 °C (approximate - calculated from water solubility and vapor pressure)
?? ??
agriculture
environmental
InChI
1S/C9H6Cl6O4S/c10-5-6(11)8(13)4-2-19-20(16,17)18-1-3(4)7(5,12)9(8,14)15/h3-4H,1-2H2/t3,4,7-,8+
InChIKey
AAPVQEMYVNZIOO-WINLOITPSA-N
SMILES
ClC1=C(Cl)[C@]2(Cl)C3COS(=O)(=O)OCC3[C@@]1(Cl)C2(Cl)Cl
EPA
Endosulfan sulfate (1031-07-8)
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  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? T+,N,Xn,F,T
?? ???? ?? 28-50/53-67-65-62-51/53-48/20-38-11-39/23/24/25-23/24/25
????? 22-24/25-45-60-61-62-36/37-16-7-33-29-9
????(UN No.) 2761
WGK ?? 3
RTECS ?? RB9150000
?? ?? 6.1(a)
???? II
???? ??? 6.1A - Combustible acute toxic Cat. 1 and 2
very toxic hazardous materials
Hazard Classifications Acute Tox. 2 Dermal
Acute Tox. 2 Inhalation
Acute Tox. 2 Oral
Aquatic Acute 1
Aquatic Chronic 1
?? ?? ??? 1031-07-8(Hazardous Substances Data)
????(GHS): Skull and Crossbones (GHS06)Environment (GHS09)
?? ?: Danger
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H410 ??? ??? ?? ????? ?? ??? ?? ????? ?? - ?? ?? 1 ?? P273, P391, P501
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P260 ??·?·??·???·??·...·????? ???? ???.
P262 ?, ??, ??? ?? ??? ???.
P273 ???? ???? ???.
P280 ????/???/???/?????? ?????.
NFPA 704
0
4 0

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Endosulfan Sulfate is a pesticide used in the control and protection of plant and vegetation.

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Water solubility - <1 mg/L at 72°F.

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Insoluble in water.

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ENDOSULFAN SULFATE is an organochlorine and cyclodiene. ENDOSULFAN SULFATE is also a sulfite ester. Corrosive to iron. Hydrolyzed by aqueous alkali or acid, generating sulfur dioxide. Incompatible with strong oxidizing and reducing agents. Also incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides. As an ester, ENDOSULFAN SULFATE will hydrolyze to form sulfur dioxide and diol; reaction is more rapid under basic conditions.

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Highly toxic, may be fatal if inhaled, swallowed or absorbed through skin. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

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Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Containers may explode when heated. Runoff may pollute waterways.

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Soil. A mixed culture of soil microorganisms biodegraded endosulfan sulfate to endosulfan ether, endosulfan-a-hydroxy ether and endosulfan lactone (Verschueren, 1983). Indigenous microorganisms obtained from a sandy loam degraded endosulfan sulfate (a metabolite of a- and b-endosulfan) to endosulfan diol. This diol was converted to endosulfan a-hydroxy ether and trace amounts of endosulfan ether and both were degraded to endosulfan lactone (Miles and Moy, 1979). Using settled domestic wastewater inoculum, endosulfan sulfate (5 and 10 mg/L) did not degrade after 28 days of incubation at 25°C (Tabak et al., 1981).
Plant. In tobacco leaves, endosulfan sulfate was converted to a-endosulfan which subsequently hydrolyzed into endosulfandiol (Chopra and Mahfouz, 1977).

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