Parachlorobenzotrifluoride

Last updated
Parachlorobenzotrifluoride
Parachlorobenzotrifluoride.svg
Names
Preferred IUPAC name
1-Chloro-4-(trifluoromethyl)benzene
Identifiers
3D model (JSmol)
AbbreviationsPCBTF
510203
ChemSpider
ECHA InfoCard 100.002.438 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 202-681-1202-681-1
MeSH C037723
PubChem CID
UNII
UN number 2234
  • InChI=1S/C7H4ClF3/c8-6-3-1-5(2-4-6)7(9,10)11/h1-4H X mark.svgN
    Key: QULYNCCPRWKEMF-UHFFFAOYSA-N X mark.svgN
  • InChI=1/C7H4ClF3/c8-6-3-1-5(2-4-6)7(9,10)11/h1-4H
    Key: QULYNCCPRWKEMF-UHFFFAOYAI
  • C1=CC(=CC=C1C(F)(F)F)Cl
Properties
C7H4ClF3
Molar mass 180.55 g·mol−1
AppearanceColorless liquid
Melting point −36 °C (−33 °F; 237 K)
Boiling point 139 °C (282 °F; 412 K)
0
Vapor pressure 7.9
0.0347
Hazards
GHS labelling:
GHS-pictogram-flamme.svg GHS-pictogram-exclam.svg GHS-pictogram-pollu.svg
Warning
H226, H315, H319, H335, H411
P210, P233, P240, P241, P242, P243, P261, P264, P271, P273, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P370+P378, P391, P403+P233, P403+P235, P405, P501
NFPA 704 (fire diamond)
NFPA 704.svgHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g. diesel fuelInstability 1: Normally stable, but can become unstable at elevated temperatures and pressures. E.g. calciumSpecial hazards (white): no code
1
2
1
Flash point 43 °C (109 °F; 316 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
X mark.svgN  verify  (what is  Yes check.svgYX mark.svgN ?)

Parachlorobenzotrifluoride is a synthetic halogenated organic chemical compound with the molecular formula C7H4ClF3. It is frequently abbreviated PCBTF. Parachlorobenzotrifluoride is a colorless liquid with a distinct aromatic odor. PCBTF has been commercially-produced since the 1960s, initially as an intermediate in the production of other petrochemicals. But since the 1990s, it has been primarily used as a solvent. [1]

Contents

History

Occidental Chemical Corporation was a leading producer and sold it as part of its Oxsol® product line, specifically under the brand name of Oxsol 100. [2] Occidental Chemical Corporation sold the OXSOL line to an Israeli company, Makhteshim Agan Industries, Ltd., in 2002. [3]

Uses

PCBTF is increasingly used as a xylene replacement in cleaners, thinners, and other aromatic hydrocarbon blends. [1]

PCBTF is used as a component (5-12%) of low volatile organic compound (VOC) compliant polyurethane finishes. [4]

The substance is used as an ink solvent in the printing industry. Parachlorobenzotrifluoride has a high capacity for dissolving many inks used by the printing industry. In most cases, up to 22 grams of ink can be dissolved in 20 grams of PCBTF.[ citation needed ] An added benefit is that parachlorobenzotrifluoride dissolves most inks faster than toluene.

Health and Environmental effects

Health effects:

In the troposphere, PCBTF has an estimated half-life of 67 days. It is transformed by reaction with photochemically-produced hydroxyl radicals to give mainly 2-chloro-5-trifluoromethylphenol. [1]

Regulation

PCBTF currently has VOC Exempt status from the U.S. Environmental Protection Agency. [5] However, California's Office of Environmental Health Hazard Assessment (OEHHA) has adopted inhalation risk factors for PCBTF as of June 2019, which could have implications for its ongoing VOC Exempt status. [6] [7]

Related Research Articles

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References

  1. 1 2 3 Rayner-Canham, Geoff (March 2014). "Para-Chlorobenzotrifluoride (PCBTF) – the 'super-solvent'". Chem 13 News Magazine. The University of Waterloo. Retrieved 14 December 2022.
  2. 1 2 MSDS provided by Islechem
  3. ↑ "Trifluoromethylbenzene 98-08-8" (PDF). National Cancer Institute. Retrieved 14 December 2022.
  4. ↑ see MSDS for MINWAX product numbers 13025(5%) and 71029(12%) [ full citation needed ]
  5. ↑ "EPA Exempt Volatile Organic Compound: Parachlorobenzotrifluoride" (PDF). American Coatings Association. 2018-01-30. Retrieved 2019-03-20.
  6. ↑ "Chemical Listed Effective June 28, 2019 as Known to the State Of California To Cause Cancer: P-Chloro-a,a,a-Trifluorotoluene (Para-Chlorobenzotrifluoride, PCBTF)". oehha.ca.gov. Retrieved 2021-08-14.
  7. ↑ p-Chloro-α,α,α-trifluorotoluene (p-Chlorobenzotrifluoride, PCBTF) - Cancer Inhalation Unit Risk Factor Scientific Review Panel Draft - January 2020 - California Office of Environmental Health Hazard Assessment
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