JP2021509672A - 2−クロロ−1,1,1,2−テトラフルオロプロパン(HCFC−244bb)を含有する組成物 - Google Patents
2−クロロ−1,1,1,2−テトラフルオロプロパン(HCFC−244bb)を含有する組成物 Download PDFInfo
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- 239000000203 mixture Substances 0.000 title claims abstract description 55
- SMCNZLDHTZESTK-UHFFFAOYSA-N 2-chloro-1,1,1,2-tetrafluoropropane Chemical compound CC(F)(Cl)C(F)(F)F SMCNZLDHTZESTK-UHFFFAOYSA-N 0.000 title claims abstract description 38
- FXRLMCRCYDHQFW-UHFFFAOYSA-N 2,3,3,3-tetrafluoropropene Chemical compound FC(=C)C(F)(F)F FXRLMCRCYDHQFW-UHFFFAOYSA-N 0.000 claims abstract description 49
- 239000012535 impurity Substances 0.000 claims abstract description 36
- 238000009835 boiling Methods 0.000 claims abstract description 19
- OQISUJXQFPPARX-UHFFFAOYSA-N 2-chloro-3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C(Cl)=C OQISUJXQFPPARX-UHFFFAOYSA-N 0.000 claims abstract description 17
- DUAKCVSNUIDZMC-UHFFFAOYSA-N 1,1,1,2,2,3,3-heptafluorobutane Chemical compound CC(F)(F)C(F)(F)C(F)(F)F DUAKCVSNUIDZMC-UHFFFAOYSA-N 0.000 claims abstract description 16
- LDTMPQQAWUMPKS-OWOJBTEDSA-N (e)-1-chloro-3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)\C=C\Cl LDTMPQQAWUMPKS-OWOJBTEDSA-N 0.000 claims abstract description 13
- LOCOMRPWMOCMPV-UHFFFAOYSA-N 2,3-dichloro-1,1,1,2-tetrafluoropropane Chemical compound FC(F)(F)C(F)(Cl)CCl LOCOMRPWMOCMPV-UHFFFAOYSA-N 0.000 claims abstract description 11
- CDOOAUSHHFGWSA-OWOJBTEDSA-N (e)-1,3,3,3-tetrafluoroprop-1-ene Chemical compound F\C=C\C(F)(F)F CDOOAUSHHFGWSA-OWOJBTEDSA-N 0.000 claims abstract description 10
- JSECXTYNFBONSF-UHFFFAOYSA-N 3-chloro-1,1,1,2-tetrafluoropropane Chemical compound ClCC(F)C(F)(F)F JSECXTYNFBONSF-UHFFFAOYSA-N 0.000 claims abstract description 10
- MSSNHSVIGIHOJA-UHFFFAOYSA-N pentafluoropropane Chemical compound FC(F)CC(F)(F)F MSSNHSVIGIHOJA-UHFFFAOYSA-N 0.000 claims abstract description 10
- INEMUVRCEAELBK-UHFFFAOYSA-N 1,1,1,2-tetrafluoropropane Chemical compound CC(F)C(F)(F)F INEMUVRCEAELBK-UHFFFAOYSA-N 0.000 claims abstract description 9
- PREWBNUKNNTMHC-UHFFFAOYSA-N 2-chloro-1,1,1,4,4,4-hexafluorobutane Chemical compound FC(F)(F)CC(Cl)C(F)(F)F PREWBNUKNNTMHC-UHFFFAOYSA-N 0.000 claims abstract description 8
- LDTMPQQAWUMPKS-UPHRSURJSA-N (z)-1-chloro-3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)\C=C/Cl LDTMPQQAWUMPKS-UPHRSURJSA-N 0.000 claims abstract description 7
- FDOPVENYMZRARC-UHFFFAOYSA-N 1,1,1,2,2-pentafluoropropane Chemical compound CC(F)(F)C(F)(F)F FDOPVENYMZRARC-UHFFFAOYSA-N 0.000 claims abstract description 7
- MDNLZVVUMKSEKO-UHFFFAOYSA-N 1,1,1-trichloro-3,3,3-trifluoropropane Chemical class FC(F)(F)CC(Cl)(Cl)Cl MDNLZVVUMKSEKO-UHFFFAOYSA-N 0.000 claims abstract description 7
- NUPBXTZOBYEVIR-UHFFFAOYSA-N 1,1,2,3,3,4,4-heptafluorobut-1-ene Chemical compound FC(F)C(F)(F)C(F)=C(F)F NUPBXTZOBYEVIR-UHFFFAOYSA-N 0.000 claims abstract description 7
- SXKNYNUXUHCUHX-UHFFFAOYSA-N 1,1,2,3,3,4-hexafluorobut-1-ene Chemical compound FCC(F)(F)C(F)=C(F)F SXKNYNUXUHCUHX-UHFFFAOYSA-N 0.000 claims abstract description 7
- QDJDUXFLHIPMOX-UHFFFAOYSA-N 1,2,2-trichloro-1,1-difluoropropane Chemical compound CC(Cl)(Cl)C(F)(F)Cl QDJDUXFLHIPMOX-UHFFFAOYSA-N 0.000 claims abstract description 7
- OMMADTGFNSRNEJ-UHFFFAOYSA-N 2,2,3-trichloro-1,1,1-trifluoropropane Chemical compound FC(F)(F)C(Cl)(Cl)CCl OMMADTGFNSRNEJ-UHFFFAOYSA-N 0.000 claims abstract description 7
- OHMHBGPWCHTMQE-UHFFFAOYSA-N 2,2-dichloro-1,1,1-trifluoroethane Chemical compound FC(F)(F)C(Cl)Cl OHMHBGPWCHTMQE-UHFFFAOYSA-N 0.000 claims abstract description 7
- JYNCTFQDWJMJDI-UHFFFAOYSA-N 2-chloro-1,1,1,3,3-pentafluoropropane Chemical compound FC(F)C(Cl)C(F)(F)F JYNCTFQDWJMJDI-UHFFFAOYSA-N 0.000 claims abstract description 7
- IZHPSCJEIFFRLN-UHFFFAOYSA-N 3,3,4,4,4-pentafluorobut-1-ene Chemical compound FC(F)(F)C(F)(F)C=C IZHPSCJEIFFRLN-UHFFFAOYSA-N 0.000 claims abstract description 7
- FLWOHKATSIAAKC-UHFFFAOYSA-N 4-chloro-1,1,2,3,3,4-hexafluorobut-1-ene Chemical compound FC(Cl)C(F)(F)C(F)=C(F)F FLWOHKATSIAAKC-UHFFFAOYSA-N 0.000 claims abstract description 7
- KAVGMUDTWQVPDF-UHFFFAOYSA-N perflubutane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)F KAVGMUDTWQVPDF-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229950003332 perflubutane Drugs 0.000 claims abstract description 7
- PFFGXVGPSGJOBV-UHFFFAOYSA-N 1,1,1,3-tetrafluoropropane Chemical compound FCCC(F)(F)F PFFGXVGPSGJOBV-UHFFFAOYSA-N 0.000 claims abstract description 6
- NDMMKOCNFSTXRU-UHFFFAOYSA-N 1,1,2,3,3-pentafluoroprop-1-ene Chemical compound FC(F)C(F)=C(F)F NDMMKOCNFSTXRU-UHFFFAOYSA-N 0.000 claims abstract description 6
- AUCISWTVFIKMCZ-UHFFFAOYSA-N 1-chloro-1,1,2,2-tetrafluoropropane Chemical compound CC(F)(F)C(F)(F)Cl AUCISWTVFIKMCZ-UHFFFAOYSA-N 0.000 claims abstract description 6
- ISCYUDAHBJMFNT-UHFFFAOYSA-N 1,1-dichloro-3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C=C(Cl)Cl ISCYUDAHBJMFNT-UHFFFAOYSA-N 0.000 claims abstract description 5
- DCWQLZUJMHEDKD-UHFFFAOYSA-N 2,2-dichloro-1,1,1-trifluoropropane Chemical compound CC(Cl)(Cl)C(F)(F)F DCWQLZUJMHEDKD-UHFFFAOYSA-N 0.000 claims abstract description 5
- QJMGASHUZRHZBT-UHFFFAOYSA-N 2,3-dichloro-1,1,1-trifluoropropane Chemical compound FC(F)(F)C(Cl)CCl QJMGASHUZRHZBT-UHFFFAOYSA-N 0.000 claims abstract description 5
- HXNJCCYKKHPFIO-UHFFFAOYSA-N 3-chloro-1,1,2,3-tetrafluoroprop-1-ene Chemical compound FC(Cl)C(F)=C(F)F HXNJCCYKKHPFIO-UHFFFAOYSA-N 0.000 claims abstract description 5
- 150000008282 halocarbons Chemical class 0.000 claims abstract description 5
- 238000010586 diagram Methods 0.000 abstract description 7
- XPRPUIGRQWCMGD-UHFFFAOYSA-N 2,3-dichloro-1,1-difluoroprop-1-ene Chemical compound FC(F)=C(Cl)CCl XPRPUIGRQWCMGD-UHFFFAOYSA-N 0.000 abstract description 6
- 238000000034 method Methods 0.000 description 36
- 238000004821 distillation Methods 0.000 description 24
- 238000004519 manufacturing process Methods 0.000 description 14
- 239000007788 liquid Substances 0.000 description 13
- 239000000243 solution Substances 0.000 description 10
- 239000000047 product Substances 0.000 description 9
- 239000002904 solvent Substances 0.000 description 8
- 230000008901 benefit Effects 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 238000000926 separation method Methods 0.000 description 6
- 238000010533 azeotropic distillation Methods 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000007033 dehydrochlorination reaction Methods 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- -1 heat transfer media Substances 0.000 description 4
- 238000010792 warming Methods 0.000 description 4
- UMGQVBVEWTXECF-UHFFFAOYSA-N 1,1,2,3-tetrachloroprop-1-ene Chemical compound ClCC(Cl)=C(Cl)Cl UMGQVBVEWTXECF-UHFFFAOYSA-N 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000006356 dehydrogenation reaction Methods 0.000 description 3
- 239000007791 liquid phase Substances 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 239000012808 vapor phase Substances 0.000 description 3
- ZPIFKCVYZBVZIV-UHFFFAOYSA-N 3-chloro-1,1,1-trifluoropropane Chemical compound FC(F)(F)CCCl ZPIFKCVYZBVZIV-UHFFFAOYSA-N 0.000 description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 206010016256 fatigue Diseases 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- 238000004508 fractional distillation Methods 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000003507 refrigerant Substances 0.000 description 2
- 238000007086 side reaction Methods 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- SDJAVCQWZJAUHT-UHFFFAOYSA-N 1,1,1,2,2,3,3,4-octafluorohexane Chemical class CCC(F)C(F)(F)C(F)(F)C(F)(F)F SDJAVCQWZJAUHT-UHFFFAOYSA-N 0.000 description 1
- PGJHURKAWUJHLJ-UHFFFAOYSA-N 1,1,2,3-tetrafluoroprop-1-ene Chemical compound FCC(F)=C(F)F PGJHURKAWUJHLJ-UHFFFAOYSA-N 0.000 description 1
- WHPKSWFREPSUCO-UHFFFAOYSA-N 1,2-dichloro-1,2,3,3-tetrafluoropropane Chemical class FC(F)C(F)(Cl)C(F)Cl WHPKSWFREPSUCO-UHFFFAOYSA-N 0.000 description 1
- LDTMPQQAWUMPKS-UHFFFAOYSA-N 1-chloro-3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C=CCl LDTMPQQAWUMPKS-UHFFFAOYSA-N 0.000 description 1
- VJGCZWVJDRIHNC-UHFFFAOYSA-N 1-fluoroprop-1-ene Chemical compound CC=CF VJGCZWVJDRIHNC-UHFFFAOYSA-N 0.000 description 1
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
- FDMFUZHCIRHGRG-UHFFFAOYSA-N 3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C=C FDMFUZHCIRHGRG-UHFFFAOYSA-N 0.000 description 1
- PLTIOZOVDUUXDQ-UHFFFAOYSA-N 3,3-dichloro-1,1,1-trifluoropropane Chemical class FC(F)(F)CC(Cl)Cl PLTIOZOVDUUXDQ-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 238000000998 batch distillation Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001944 continuous distillation Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000007701 flash-distillation Methods 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 238000000622 liquid--liquid extraction Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C19/00—Acyclic saturated compounds containing halogen atoms
- C07C19/08—Acyclic saturated compounds containing halogen atoms containing fluorine
- C07C19/10—Acyclic saturated compounds containing halogen atoms containing fluorine and chlorine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/25—Preparation of halogenated hydrocarbons by splitting-off hydrogen halides from halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C21/00—Acyclic unsaturated compounds containing halogen atoms
- C07C21/02—Acyclic unsaturated compounds containing halogen atoms containing carbon-to-carbon double bonds
- C07C21/18—Acyclic unsaturated compounds containing halogen atoms containing carbon-to-carbon double bonds containing fluorine
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Detergent Compositions (AREA)
Abstract
Description
2244bb成分後の表1に列挙したものに加えて、その他の重質分の非限定的な例としては、クロロヘキサフルオロブテン(HFO−1326異性体)、ヘキサフルオロブテン(HFO−1336異性体)、ペンタフルオロブテン(HFO−1345異性体)、ヘプタフルオロブテン(HFO−1327異性体)、テトラフルオロヘキサン(HFC−5−11−4異性体)、1,3,3,3−テトラフルオロプロパン(HFC−254fb)、クロロヘキサフルオロブタン(HFC−346異性体)、オクタフルオロペンタン(HFC−458異性体)、オクタフルオロヘキセン、2,2−ジクロロ−1,1,1−トリフルオロエタン(HCFC−123)、(Z)−1−クロロ−3,3,3−トリフルオロプロペン(HCFO−1233zd(Z))、C5H2F10異性体、C6H2F8異性体、C6H4F8異性体、デカフルオロブタン(C4F10)、C6H3F7異性体、C6H3F9異性体、ジクロロジフルオロプロペン(HCFO−1232異性体)、トリクロロトリフルオロプロパン(HCFC−233異性体)、C6H3Cl2F7異性体、トリクロロジフルオロプロパン(HCFC−242異性体)、C8H3F7異性体及びタールが挙げられる。
Claims (14)
- 組成物であって、
2−クロロ−1,1,1,2−テトラフルオロプロパン(HCFC−244bb)と、
少なくとも1種の2,3,3,3−テトラフルオロプロペン(HFO−1234yf)、ペンタフルオロプロペン(HFO−1225ye異性体(複数可))、1,3,3,3−テトラフルオロプロペン(HFO−1234ze異性体(複数可))、1,1,1,2,2−ペンタフルオロプロパン(HFC−245cb)、1,1,1,2−テトラフルオロプロパン(HFC−254eb)、2−クロロ−3,3,3−トリフルオロプロペン(HCFO−1233xf)、1−クロロ−1,1,2,2−テトラフルオロプロパン(HCFC−244cc)、クロロテトラフルオロプロペン(HCFO−1224異性体)、E−1−クロロ−3,3,3−トリフルオロプロペン(HCFO−1233zdE)、1,1,1,3,3−ペンタフルオロプロパン(HFC−245fa)、ヘプタフルオロブタン(HFC−347異性体)、2−クロロ−1,1,1,3,3−ペンタフルオロプロパン(HFC−235da)、3−クロロ−1,1,1,2−テトラフルオロプロパン(HCFC−244eb)、3−クロロ−3,3,3−トリフルオロプロパン(HCFC−253fb)、ジクロロトリフルオロプロペン(HCFO−1223異性体)、2,3−ジクロロ−1,1,1,2−テトラフルオロプロパン(HCFC−234bb)、2,2−ジクロロ−1,1,1−トリフルオロプロパン(HCFC−243db)、クロロヘキサフルオロブテン(HFO−1326異性体)、ヘキサフルオロブテン(HFO−1336異性体)、ペンタフルオロブテン(HFO−1345異性体)、ヘプタフルオロブテン(HFO−1327異性体)、テトラフルオロヘキサン(HFC−5−11−4異性体)、1,3,3,3−テトラフルオロプロパン(HFC−254fb)、クロロヘキサフルオロブタン(HFC−346異性体)、オクタフルオロペンタン(HFC−458異性体)、オクタフルオロヘキセン、2,2−ジクロロ−1,1,1−トリフルオロエタン(HCFC−123)、(Z)−1−クロロ−3,3,3−トリフルオロプロペン(HCFO−1233zd(Z))、C5H2F10異性体、C6H2F8異性体、C6H4F8異性体、デカフルオロブタン(C4F10)、C6H3F7異性体、C6H3F9異性体、ジクロロジフルオロプロペン(HCFO−1232異性体)、トリクロロトリフルオロプロパン(HCFC−233異性体)、C6H3Cl2F7異性体、トリクロロジフルオロプロパン(HCFC−242異性体)、C8H3F7異性体又は約15℃を超える沸点を有する長鎖ハロゲン化炭化水素を含む、少なくとも1種の不純物と、を含む組成物。 - 前記少なくとも1種の不純物が、約0.0001重量%〜約2.0重量%の量で存在する、請求項1に記載の組成物。
- 前記少なくとも1種の不純物が、約0.0005重量%〜約0.5重量%の量で存在する、請求項2に記載の組成物。
- 前記少なくとも1種の不純物が、約0.001重量%〜約0.05重量%の量で存在する、請求項3に記載の組成物。
- 前記組成物が、少なくとも2種の異なる不純物を含む、請求項1に記載の組成物。
- 前記少なくとも2種の異なる不純物が第1の不純物を含み、前記第1の不純物が253fbである、請求項5に記載の組成物。
- 前記少なくとも1種の不純物がヘプタフルオロブタンである、請求項1に記載の組成物。
- 前記ヘプタフルオロブタンが、1,1,1,2,2,3,3−ヘプタフルオロブタンである、請求項7に記載の組成物。
- 前記第2の不純物がヘプタフルオロブタンである、請求項6に記載の組成物。
- 前記253fbと前記ヘプタフルオロブタンとの合計量が、0.0005重量%〜0.5重量%の量で存在する、請求項9に記載の組成物。
- 前記253fbと前記ヘプタフルオロブタンとの合計量が、0.001重量%〜0.2重量%の量で存在する、請求項10に記載の組成物。
- 前記253fbと前記ヘプタフルオロブタンとの合計量が、0.0015重量%〜0.12重量%の量で存在する、請求項11に記載の組成物。
- 前記HCFC−244bbが、95重量%〜99.999重量%の量で存在する、請求項1に記載の組成物。
- 前記HCFC−244bbが、98.0重量%〜99.0重量%の量で存在する、請求項1に記載の組成物。
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Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2023180036A JP2024010021A (ja) | 2018-01-08 | 2023-10-19 | 2-クロロ-1,1,1,2-テトラフルオロプロパン(HCFC-244bb)を含有する組成物 |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US15/864,722 | 2018-01-08 | ||
US15/864,722 US10246389B1 (en) | 2018-01-08 | 2018-01-08 | Compositions containing 2-chloro-1,1,1,2-tetrafluoropropane (HCFC-244bb) |
PCT/US2019/012615 WO2019136408A1 (en) | 2018-01-08 | 2019-01-08 | COMPOSITIONS CONTAINING 2-chloro-1,1,1,2-tetrafluoropropane (HCFC-244bb) |
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JP2023180036A Division JP2024010021A (ja) | 2018-01-08 | 2023-10-19 | 2-クロロ-1,1,1,2-テトラフルオロプロパン(HCFC-244bb)を含有する組成物 |
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JP7372923B2 JP7372923B2 (ja) | 2023-11-01 |
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JP2020537189A Active JP7372923B2 (ja) | 2018-01-08 | 2019-01-08 | 2-クロロ-1,1,1,2-テトラフルオロプロパン(HCFC-244bb)を含有する組成物 |
JP2023180036A Pending JP2024010021A (ja) | 2018-01-08 | 2023-10-19 | 2-クロロ-1,1,1,2-テトラフルオロプロパン(HCFC-244bb)を含有する組成物 |
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EP (1) | EP3737659A4 (ja) |
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US10246389B1 (en) | 2018-01-08 | 2019-04-02 | Honeywell International Inc. | Compositions containing 2-chloro-1,1,1,2-tetrafluoropropane (HCFC-244bb) |
AU2021217149A1 (en) * | 2020-02-07 | 2022-07-07 | The Chemours Company Fc, Llc | Compositions comprising 2,3,3,3 tetrafluoropropene and methods for making and using the compositions |
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JP2024010021A (ja) | 2024-01-23 |
US20190210945A1 (en) | 2019-07-11 |
CN117986083A (zh) | 2024-05-07 |
CN117986082A (zh) | 2024-05-07 |
WO2019136408A1 (en) | 2019-07-11 |
KR20200098687A (ko) | 2020-08-20 |
US10870615B2 (en) | 2020-12-22 |
JP7372923B2 (ja) | 2023-11-01 |
EP3737659A1 (en) | 2020-11-18 |
MX2020006974A (es) | 2020-09-09 |
US10246389B1 (en) | 2019-04-02 |
EP3737659A4 (en) | 2021-11-17 |
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