Detail of > 75-68-3
- MSDS Download

- CAS Number:
- 75-68-3
- Name:
Ethane,1-chloro-1,1-difluoro-
- Superlist Name:
- 1-Chloro-1,1-difluoroethane
- Formula:
- C2H3ClF2
- Molecular Structure:

- Synonyms:
- 1,1-Difluoro-1-chloroethane;CFC 142b;Daiflon 142b;Dymel 142;F 142b;FC142b;FKW 142b;Freon 142b;Fron 142b;Genetron 101;Genetron 142b;HCFC 142b;HFA 142b;Propellant 142B;R 142b;Solkane 142b;a-Chloroethylidene fluoride;
- Molecular Weight:
- 100.50
- EINECS:
- 200-891-8
- Density:
- 1.198 g/cm3
- Melting Point:
- -131 °C
- Boiling Point:
- -9 °C
- Appearance:
- colourless gas
- Hazard Symbols:
F+,
N,
Xi- Risk Codes:
- 12-59
- Safety:
- 38-59Details
- Transport Information:
- UN 2517 2.1
- Deleted CAS:
- 65762-25-6
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Reference
- Aerosol sprays
- Aerosol sprays. Daimon, Shigeo; Deguchi, Takayuki; Okamura, Kazuo (Daikin Kogyo Co., Ltd., Japan). Japan. Kokai JP 53062789 5 Jun 1978 Showa, 5 pp. (Japanese). (Japan). CODEN: JKXXAF. CLASS: IC: C09K003-30. APPLICATION: JP 76-138747 17 Nov 1976. DOCUMENT TYPE: Patent CA Section: 62 (Essential Oils and Cosmetics) Section cross-reference(s): 5 Aerosol sprays for hair and insecticidal prepns. contain >2 fluorocarbon propellants with b.p. <9° and difference of b.p. for the propellants < 40°. Fluorocarbons such as R-12 (dichlorodifluoromethane) [75-71-8], R-22 (monochlorodifluoromethane) [75-45-6], and R-142b [75-68-3] can be used. The prepns. show a high aerosolization rate, and thus require minimal amts. of fluorocarbon propellants. E.g., a hair spray consists of 100 g 3 wt.% poly(vinyl pyrrolidone) in EtOH, and 70 g of a 70/30 R-22/R-142b mixt.
- Vinylidene fluoride
- Vinylidene fluoride. (Solvay et Cie., Belg.). Belg. BE 844822 1 Dec 1977, 25 pp. (Unavailable). (Belgium). CODEN: BEXXAL. CLASS: IC: C07C. PRIORITY: LU 75-73162 6 Aug 1975. DOCUMENT TYPE: Patent CA Section: 35 (Synthetic High Polymers) Section cross-reference(s): 23 1,1-Difluoroethane (I) [75-37-6] was photochem. chlorinated in the gas phase to give 1-chloro-1,1-difluoroethane [75-68-3] which was taken up in a solvent and processed through an absorption system to sep. HCl prior to pyrolysis to give vinylidene fluoride (III) [75-38-7]. Thus, I was fed at 1 kmol/h with 1.05 kmol/h Cl to a system of 4 chlorination zones at 40.degree. contg. UV lamps. The reaction mixt. was sprayed with 2.5 kmol/h CCl4. The product obtained, which contained II 0.97, HCl 1.058, CCl4 0.79 kmol/h and other haloethanes, was fed to an absorption column with 12.9 kcal CCl4 at -6.degree. and 1 atm. The column was pressurized to give a product steam contg. a conc. of II which was pyrolyzed at 550.degree. to give III.
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