![]() chlorohexane structure
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Common Name | chlorohexane | ||
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CAS Number | 544-10-5 | Molecular Weight | 120.620 | |
Density | 0.9±0.1 g/cm3 | Boiling Point | 133.9±3.0 °C at 760 mmHg | |
Molecular Formula | C6H13Cl | Melting Point | −94 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 26.7±0.0 °C | |
Symbol |
![]() GHS02 |
Signal Word | Warning |
QSPR modeling of octanol/water partition coefficient for vitamins by optimal descriptors calculated with SMILES.
Eur. J. Med. Chem. 43 , 714-40, (2008) Simplified molecular input line entry system (SMILES) has been utilized in constructing quantitative structure-property relationships (QSPR) for octanol/water partition coefficient of vitamins and organic compounds of different classes by optimal descriptors.... |
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Evaluation of injection methods for fast, high peak capacity separations with low thermal mass gas chromatography.
J. Chromatogr. A. 1392 , 82-90, (2015) Low thermal mass gas chromatography (LTM-GC) was evaluated for rapid, high peak capacity separations with three injection methods: liquid, headspace solid phase micro-extraction (HS-SPME), and direct vapor. An Agilent LTM equipped with a short microbore capil... |
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Post-Translational Modification of Bionanoparticles as a Modular Platform for Biosensor Assembly.
ACS Nano 9 , 8554-61, (2015) Context driven biosensor assembly with modular targeting and detection moieties is gaining significant attentions. Although protein-based nanoparticles have emerged as an excellent platform for biosensor assembly, current strategies of decorating bionanoparti... |
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Temperature influence on 4-aminophthalimide emission in 1-chloroalkanes plus water mixtures.
J. Phys. Chem. A 116(25) , 6655-63, (2012) Thermochromic emission shifts of 4-aminophthalimide (4-AP) dissolved in three 1-chloroalkanes, namely, 1-chloropropane, 1-chlorobutane, and 1-chlorohexane, together with fluorescence decays measured at different wavelengths, all solvents containing different ... |
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The role of spontaneous cap domain mutations in haloalkane dehalogenase specificity and evolution.
J. Biol. Chem. 269(26) , 17490-4, (1994) The first step in the utilization of the xenobiotic chlorinated hydrocarbon 1,2-dichloroethane by Xanthobacter autotrophicus is catalyzed by haloalkane dehalogenase (Dh1A). The enzyme hydrolyses 1-haloalkanes to the corresponding alcohols. This allows the org... |
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Catalytic mechanism of the maloalkane dehalogenase LinB from Sphingomonas paucimobilis UT26.
J. Biol. Chem. 278(46) , 45094-100, (2003) Haloalkane dehalogenases are bacterial enzymes capable of carbon-halogen bond cleavage in halogenated compounds. To obtain insights into the mechanism of the haloalkane dehalogenase from Sphingomonas paucimobilis UT26 (LinB), we studied the steady-state and p... |
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Kinetic characterization and X-ray structure of a mutant of haloalkane dehalogenase with higher catalytic activity and modified substrate range.
Biochemistry 35(40) , 13186-95, (1996) Conversion of halogenated aliphatics by haloalkane dehalogenase proceeds via the formation of a covalent alkyl-enzyme intermediate which is subsequently hydrolyzed by water. In the wild type enzyme, the slowest step for both 1,2-dichloroethane and 1,2-dibromo... |
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Orthogonal protein decoration of DNA nanostructures.
Small 7(22) , 3211-8, (2011) The development of robust DNA-protein coupling techniques is mandatory for applications of DNA nanostructures in biomedical diagnostics, fundamental biochemistry, and other fields in biomolecular nanosciences. The use of self-labeling fusion proteins, which a... |
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Thermochemical investigations of associated solutions: 5. Calculation of solute-solvent equilibrium constants from solubility in mixtures containing two complexing solvents.
J. Pharm. Sci. 76(7) , 575-9, (1987) Solubilities are reported for carbazole in binary dibutyl ether plus 1-chlorohexane mixtures at 25 degrees C. Results of these measurements are compared with solution models developed for solubility in systems containing specific solute-solvent interactions. ... |
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Performance of supported nickel and other metal catalysts in the hydrodechlorination of chlorobenzene and 1-chlorohexane. de Jong V and Louw R.
Appl. Catal. A Gen. 271(1) , 153-63, (2004)
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