| Identification | Back Directory | [Name]
ENDOSULFAN SULFATE | [CAS]
1031-07-8 | [Synonyms]
THIODAN SULFATE
BENZOEPIN SULFATE
ENDOSULFAN SULFATE
Enoosulfan sulfate
hiepin-3,3-dioxide
ENDOSULFAN-SULPHATE
ENDOSULPHANSULPHATE
xahydro-,3,3-dioxide
Endosulfan Impurity 1
endosulfancyclicsulfate
endosulfan sulfate solution
Endosulfan sulfate Standard
ENDOSULFAN SULFATE, 50MG, NEAT
ENDOSULFAN SULFATE, 100MG, NEAT
Endosulfan-sulfate Solution, 100ppm
Benzoepin Sulfate Reference Material
Endosulfan Sulfate Solution, 1000ppm
Endosulfan sulfate 50mg [1031-07-8]
Endosulfan Sulfate @100 μg/mL in MeOH
Endosulfan-sulfate@1000 μg/mL in Acetone
ENDOSULFAN SULFATE, 1X1ML, MEOH, 20UG/ML
1,4,5,6,7,7-hexachloro-5-norbornene-cyclicsulfate
3-dimethanol,1,4,5,6,7,7-hexachloro-5-norbornene-cyclicsulfate
5-Norbornene-2,3-dimethanol, 1,4,5,6,7,7-hexachloro-, cyclic sulfate
6,9-methano-2,4,3-benzodioxathiepin,6,7,8,9,10,10-hexachloro-1,5,5a,6,9,9a-he
6,7,8,9,10,10-hexachloro-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxat
6,7,8,9,10,10-HEXACHLORO-1,5,5A,6,9,9A-HEXAHYDRO-6,9-METHANO-2,3,4-BENZODIOXYTHIEPIN-3,3-DIOXIDE
6,7,8,9,10,10-HEXACHLORO-1,5,5A,6,9,9A-HEXAHYDRO-6,9-METHANO-2,4,3-BENZODIOXATHIEPIN-3,3-DIOXIDE
1,5,5a,6,9,9a-Hexahydro-6,9-methano-6,7,8,9,10,10-hexachloro-2,4,3-benzodioxathiepin 3,3-dioxide
6,9-Methano-2,4,3-benzodioxathiepin, 6,7,8,9,10,10-hexachloro-1,5,5a,6,9,9a-hexahydro-, 3,3-dioxide | [EINECS(EC#)]
623-765-8 | [Molecular Formula]
C9H6Cl6O4S | [MDL Number]
MFCD00151179 | [MOL File]
1031-07-8.mol | [Molecular Weight]
422.92 |
| Chemical Properties | Back Directory | [Melting point ]
147.71°C | [Boiling point ]
480.7±45.0 °C(Predicted) | [density ]
1.6835 (estimate) | [vapor pressure ]
9.75 x 10-6 mmHg at 25 °C (subcooled liquid vapor pressure calculated from GC retention time data,Hinckley et al., 1990) | [Fp ]
-26 °C | [storage temp. ]
APPROX 4°C
| [solubility ]
DMSO: Slightly Soluble,Methanol: Slightly Soluble | [form ]
Liquid | [color ]
Clear colorless | [Water Solubility ]
117 ppb (Ali, 1978) | [Henry's Law Constant]
4.64(x 10-5 atm?m3/mol) at 25 °C (approximate - calculated from water solubility and vapor pressure) | [EPA Substance Registry System]
Endosulfan sulfate (1031-07-8) |
| Hazard Information | Back Directory | [Uses]
Endosulfan Sulfate is a pesticide used in the control and protection of plant and vegetation. | [General Description]
Water solubility - <1 mg/L at 72°F. | [Air & Water Reactions]
Insoluble in water. | [Reactivity Profile]
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. | [Health Hazard]
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. | [Fire Hazard]
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. | [Environmental Fate]
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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