JPS608233A - 安定化された１，１，１−トリクロロエタン組成物 - Google Patents
安定化された１，１，１−トリクロロエタン組成物Info
- Publication number
- JPS608233A JPS608233A JP59118051A JP11805184A JPS608233A JP S608233 A JPS608233 A JP S608233A JP 59118051 A JP59118051 A JP 59118051A JP 11805184 A JP11805184 A JP 11805184A JP S608233 A JPS608233 A JP S608233A
- Authority
- JP
- Japan
- Prior art keywords
- stabilized
- trichloroethane
- compound
- furan
- composition according
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 29
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 title claims abstract description 9
- -1 epoxide compound Chemical class 0.000 claims abstract description 13
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims abstract description 9
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical group CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims abstract description 8
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 claims abstract description 8
- 125000005907 alkyl ester group Chemical group 0.000 claims abstract description 6
- 150000002828 nitro derivatives Chemical class 0.000 claims abstract description 6
- VQKFNUFAXTZWDK-UHFFFAOYSA-N 2-Methylfuran Chemical compound CC1=CC=CO1 VQKFNUFAXTZWDK-UHFFFAOYSA-N 0.000 claims description 12
- GSNUFIFRDBKVIE-UHFFFAOYSA-N 2,5-dimethylfuran Chemical compound CC1=CC=C(C)O1 GSNUFIFRDBKVIE-UHFFFAOYSA-N 0.000 claims description 4
- CPLJMYOQYRCCBY-UHFFFAOYSA-N 2-Propylfuran Chemical compound CCCC1=CC=CO1 CPLJMYOQYRCCBY-UHFFFAOYSA-N 0.000 claims description 4
- HLPIHRDZBHXTFJ-UHFFFAOYSA-N 2-ethylfuran Chemical compound CCC1=CC=CO1 HLPIHRDZBHXTFJ-UHFFFAOYSA-N 0.000 claims description 4
- 239000008346 aqueous phase Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000012074 organic phase Substances 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 150000002240 furans Chemical class 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 3
- 238000004062 sedimentation Methods 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 150000007824 aliphatic compounds Chemical class 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 238000005238 degreasing Methods 0.000 description 2
- 238000005108 dry cleaning Methods 0.000 description 2
- 125000004971 nitroalkyl group Chemical group 0.000 description 2
- MCSAJNNLRCFZED-UHFFFAOYSA-N nitroethane Chemical compound CC[N+]([O-])=O MCSAJNNLRCFZED-UHFFFAOYSA-N 0.000 description 2
- 150000002924 oxiranes Chemical class 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- JSZOAYXJRCEYSX-UHFFFAOYSA-N 1-nitropropane Chemical compound CCC[N+]([O-])=O JSZOAYXJRCEYSX-UHFFFAOYSA-N 0.000 description 1
- AFOPCURQYRRFRQ-UHFFFAOYSA-N 2-Isopropylfuran, Natural products CC(C)C1=CC=CO1 AFOPCURQYRRFRQ-UHFFFAOYSA-N 0.000 description 1
- FGLBSLMDCBOPQK-UHFFFAOYSA-N 2-nitropropane Chemical compound CC(C)[N+]([O-])=O FGLBSLMDCBOPQK-UHFFFAOYSA-N 0.000 description 1
- 241000238557 Decapoda Species 0.000 description 1
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 150000002012 dioxanes Chemical class 0.000 description 1
- 229960003750 ethyl chloride Drugs 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/38—Separation; Purification; Stabilisation; Use of additives
- C07C17/42—Use of additives, e.g. for stabilisation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
- Detergent Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8309718 | 1983-06-09 | ||
| FR8309718A FR2547296B1 (fr) | 1983-06-09 | 1983-06-09 | Compositions stabilisees de 1,1,1-trichloroethane |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS608233A true JPS608233A (ja) | 1985-01-17 |
| JPH0528211B2 JPH0528211B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1993-04-23 |
Family
ID=9289706
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59118051A Granted JPS608233A (ja) | 1983-06-09 | 1984-06-08 | 安定化された１，１，１−トリクロロエタン組成物 |
Country Status (6)
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57179128A (en) * | 1981-04-13 | 1982-11-04 | Solvay | Stabilizing composition of 1,1,1-trichloroethane |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5035045B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1970-12-26 | 1975-11-13 | ||
| BE858017A (fr) * | 1977-08-23 | 1978-02-23 | Solvay | Procede de stabilisation du 1,1,1-trichlorethane |
-
1983
- 1983-06-09 FR FR8309718A patent/FR2547296B1/fr not_active Expired
-
1984
- 1984-05-30 DE DE8484200776T patent/DE3460475D1/de not_active Expired
- 1984-05-30 EP EP84200776A patent/EP0128618B1/fr not_active Expired
- 1984-05-30 AT AT84200776T patent/ATE21381T1/de active
- 1984-06-08 ES ES533239A patent/ES533239A0/es active Granted
- 1984-06-08 JP JP59118051A patent/JPS608233A/ja active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57179128A (en) * | 1981-04-13 | 1982-11-04 | Solvay | Stabilizing composition of 1,1,1-trichloroethane |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0128618B1 (fr) | 1986-08-13 |
| JPH0528211B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1993-04-23 |
| ES8503321A1 (es) | 1985-02-16 |
| FR2547296A1 (fr) | 1984-12-14 |
| FR2547296B1 (fr) | 1986-06-13 |
| ATE21381T1 (de) | 1986-08-15 |
| ES533239A0 (es) | 1985-02-16 |
| DE3460475D1 (en) | 1986-09-18 |
| EP0128618A1 (fr) | 1984-12-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Segre et al. | A new synthesis of 6-thioctic acid (DL-α-lipoic acid) | |
| US2567621A (en) | Stabilized tetrachloroethylene composition | |
| JPS608233A (ja) | 安定化された１，１，１−トリクロロエタン組成物 | |
| Prout | Unsymmetrical Quaternary Carbon Compounds. I. The Alkylation of Ethyl 2-Cyano-3-methyl-2-pentenoate with Aliphatic Grignard Reagents | |
| US4861926A (en) | Stabilized 1,1,1-trichloroethane compositions | |
| US2533086A (en) | Hydroxymethylthianaphthene | |
| US4351973A (en) | Stabilized methylchloroform | |
| EP0008157B1 (en) | Stabilisation of chlorinated aliphatic hydrocarbons | |
| JPH0222739B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| US3076040A (en) | Stabilized solvent composition | |
| JPS6229538A (ja) | １，１，１−トリクロロエタンの安定化された組成物 | |
| FR2486967A1 (fr) | Compositions stabilisees de 1,1,1-trichloroethane | |
| US2263436A (en) | Dehydration of unsaturated aliphatic cyanides | |
| US3439051A (en) | 2,3-dihydro-1,4-dithiins as stabilizers for chlorinated hydrocarbons | |
| JPH07196545A (ja) | ハロゲン化溶媒をベースとした脱脂用組成物を安定化させる方法および添加剤 | |
| US4231968A (en) | Stabilization of 1,1,1-trichloroethane | |
| BE1005713A3 (fr) | Procede de stabilisation d'un hydrofluoroalcane et compositions comprenant au moins un hydrofluoroalcane. | |
| JP2772933B2 (ja) | １，１−ジクロル−１−フルオルエタン未精製品の安定化 | |
| US2621215A (en) | Tetrachloroethylene stabilized by 2-halothiophene | |
| US1800862A (en) | Method of separating secondary alcohols from pine oil | |
| JPH06100891A (ja) | 溶剤又はその組成物 | |
| US3475503A (en) | Stabilization of 1,1,1-trichloroethane | |
| FR2697519A1 (fr) | Procédé et additif pour la stabilisation d'une composition à base de solvants halogènes, compositions ainsi obtenues et leur application au dégraissage ou au nettoyage de pièces métalliques. | |
| FI65985C (fi) | Foer avlaegsning av fett fraon metall- och andra ytor laemplig1,1,1-trikloretan-produkt | |
| US3022346A (en) | Preparation of aliphatic-nu-chloro-nu-alkyl-amides |