374067
Sodium chlorodifluoroacetate
96%
Synonym(s):
Chlorodifluoroacetic acid sodium salt
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About This Item
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Assay
96%
mp
196-198 °C (lit.)
functional group
chloro
fluoro
SMILES string
[Na+].[O-]C(=O)C(F)(F)Cl
InChI
1S/C2HClF2O2.Na/c3-2(4,5)1(6)7;/h(H,6,7);/q;+1/p-1
InChI key
MRTAVLDNYYEJHK-UHFFFAOYSA-M
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Chemical research in toxicology, 4(2), 180-186 (1991-03-01)
1,2-Dichloro-1,1-difluoroethane (HCFC-132b) is a potential substitute for some ozone-depleting chlorofluorocarbons and a model for other 1,1,1,2-tetrahaloethanes under consideration as chlorofluorocarbon substitutes. Male Fischer 344 rats were given 10 mmol/kg HCFC-132b dissolved in corn oil by intraperitoneal injection. An NMR assay
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2(1), 62-67 (2003-03-28)
Increased UV-B through stratospheric ozone depletion leads to an increased chemical activity in the lower atmosphere (the troposphere). The effect of stratospheric ozone depletion on tropospheric ozone is small (though significant) compared to the ozone generated anthropogenically in areas already
Environmental toxicology and chemistry, 20(12), 2758-2767 (2002-01-05)
Chlorodifluoroacetic acid (CDFA) is a novel haloacetic acid (HAA) and has been recently documented in aquatic systems. It is a suspected degradation product of the refrigerants 1,1,2-trichloro-1,1-difluoroethane (CFC-113) and 1-chloro-1,1-difluoroethane (HCFC-142b). Haloacetic acids can be phytotoxic, putatively acting through inhibition
Solid state nuclear magnetic resonance, 6(2), 141-146 (1996-04-01)
The reorientation of CClF2 groups in N(CH3)4H(ClF2CCOO)2 has been studied using pulsed NQR and NMR techniques. The temperature dependence of both chlorine (35Cl) NQR and fluorine (19F) NMR spin-lattice relaxation has been measured T1Q of chlorine is attributed to the
The Journal of chemical physics, 135(12), 124307-124307 (2011-10-07)
Negative ion formation following resonant electron attachment to the three title molecules is studied by means of a beam experiment with mass spectrometric detection of the anions. All three molecules exhibit a pronounced resonance in the energy range around 1
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