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7158-32-9

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7158-32-9 Usage

Physical Form

Crystal - Powder

Uses

4,4'-OXYBISBENZOYL CHLORIDE is a useful research chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 7158-32-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7158-32:
(6*7)+(5*1)+(4*5)+(3*8)+(2*3)+(1*2)=99
99 % 10 = 9
So 7158-32-9 is a valid CAS Registry Number.

7158-32-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-carbonochloridoylphenoxy)benzoyl chloride

1.2 Other means of identification

Product number -
Other names BENZOYL CHLORIDE,p,p'-OXYBIS

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7158-32-9 SDS

7158-32-9Synthetic route

oxybis(benzoic acid)
2215-89-6

oxybis(benzoic acid)

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

Conditions
ConditionsYield
With thionyl chloride In N,N-dimethyl-formamide; toluene at 95℃; for 3h;95%
With thionyl chloride In N,N-dimethyl-formamide; toluene at 95℃; for 3h;95%
With thionyl chloride; N,N-dimethyl-formamide In toluene at 95℃; for 3h;95%
4-(4-formylphenoxy)benzaldehyde
2215-76-1

4-(4-formylphenoxy)benzaldehyde

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

Conditions
ConditionsYield
With thionyl chloride
4-(4'-cyanophenoxy)benzonitrile
6508-04-9

4-(4'-cyanophenoxy)benzonitrile

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: aqueous H2SO4
2: SOCl2
View Scheme
2,2-bis(3-amino-4-hydroxyphenyl)hexafluoropropane
83558-87-6

2,2-bis(3-amino-4-hydroxyphenyl)hexafluoropropane

benzene-1,3-dicarbonyl dichloride
99-63-8

benzene-1,3-dicarbonyl dichloride

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

poly(hexafluoro-2,2-bis(3-amino-4-hydroxyphenyl)propane-co-isophthaloyl chloride-co-4,4-oxydibenzoyl chloride)

poly(hexafluoro-2,2-bis(3-amino-4-hydroxyphenyl)propane-co-isophthaloyl chloride-co-4,4-oxydibenzoyl chloride)

Conditions
ConditionsYield
With pyridine In 1-methyl-pyrrolidin-2-one at 0 - 20℃;100%
4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

4,4'-oxy-bis(4,1-phenylene) dimethanol
2350-43-8

4,4'-oxy-bis(4,1-phenylene) dimethanol

Conditions
ConditionsYield
With lithium aluminium tetrahydride In tetrahydrofuran for 6h; Reflux;95.5%
N-[4-(pyridin-3-yl)pyrimidin-2-yl]benzene-1,4-diamine

N-[4-(pyridin-3-yl)pyrimidin-2-yl]benzene-1,4-diamine

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

4,4′-oxybis[N-(3-{[4-(pyridin-3-yl)pyrimidin-2-yl]amino}phenyl)benzamide]

4,4′-oxybis[N-(3-{[4-(pyridin-3-yl)pyrimidin-2-yl]amino}phenyl)benzamide]

Conditions
ConditionsYield
Stage #1: N-[4-(pyridin-3-yl)pyrimidin-2-yl]benzene-1,4-diamine With triethylamine In tetrahydrofuran for 0.5h;
Stage #2: 4,4'-bis(chlorocarbonyl)diphenyl oxide In tetrahydrofuran at 20℃;
93%
2,3-dihydroxypropyl methacrylate
5919-74-4

2,3-dihydroxypropyl methacrylate

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

C28H30O11

C28H30O11

Conditions
ConditionsYield
With N,N,N,N,-tetramethylethylenediamine; 2,6-di-tert-butyl-4-methyl-phenol In dichloromethane at -78℃; for 5h;92%
4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

1-[(2-methyl-5-methylenehydroxy-3-thienyl)]-2-[(2-methyl-5-methylenehydroxy-3-thienyl)]perfluorocyclopentene
216864-70-9

1-[(2-methyl-5-methylenehydroxy-3-thienyl)]-2-[(2-methyl-5-methylenehydroxy-3-thienyl)]perfluorocyclopentene

Reaxys ID: 11391242

Reaxys ID: 11391242

Conditions
ConditionsYield
91%
4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

6-methyl-1-N-(4-(pyridin-3-yl)pyrimidin-2-yl)benzene-1,3-diamine
152460-10-1

6-methyl-1-N-(4-(pyridin-3-yl)pyrimidin-2-yl)benzene-1,3-diamine

4,4′-oxybis[N-(4-methyl-3-{[4-(pyridin-3-yl)pyrimidin-2-yl]amino}phenyl)benzamide]

4,4′-oxybis[N-(4-methyl-3-{[4-(pyridin-3-yl)pyrimidin-2-yl]amino}phenyl)benzamide]

Conditions
ConditionsYield
Stage #1: 6-methyl-1-N-(4-(pyridin-3-yl)pyrimidin-2-yl)benzene-1,3-diamine With triethylamine In tetrahydrofuran for 0.5h;
Stage #2: 4,4'-bis(chlorocarbonyl)diphenyl oxide In tetrahydrofuran at 20℃;
89%
N,N-(4-methyl-3-aminophenyl)[4-(pyridin-3-yl)-pyrimidin-2-yl]amine
571187-03-6

N,N-(4-methyl-3-aminophenyl)[4-(pyridin-3-yl)-pyrimidin-2-yl]amine

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

4,4′-oxybis[N-(2-methyl-5-{[4-(pyridin-3-yl)pyrimidin-2-yl]amino}phenyl)benzamide]

4,4′-oxybis[N-(2-methyl-5-{[4-(pyridin-3-yl)pyrimidin-2-yl]amino}phenyl)benzamide]

Conditions
ConditionsYield
Stage #1: N,N-(4-methyl-3-aminophenyl)[4-(pyridin-3-yl)-pyrimidin-2-yl]amine With triethylamine In tetrahydrofuran for 0.5h;
Stage #2: 4,4'-bis(chlorocarbonyl)diphenyl oxide In tetrahydrofuran at 20℃;
86%
ammonium thiocyanate
1147550-11-5

ammonium thiocyanate

ethanolamine
141-43-5

ethanolamine

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

4,4′-oxybis(N-((2-hydroxyethyl)-carbamothioyl)benzamide)

4,4′-oxybis(N-((2-hydroxyethyl)-carbamothioyl)benzamide)

Conditions
ConditionsYield
Stage #1: ammonium thiocyanate; 4,4'-bis(chlorocarbonyl)diphenyl oxide With PEG-400 In dichloromethane at 20℃; for 1h;
Stage #2: ethanolamine In dichloromethane for 1h;
85%
Stage #1: ammonium thiocyanate; 4,4'-bis(chlorocarbonyl)diphenyl oxide With PEG-400 In dichloromethane at 20℃; for 1h;
Stage #2: ethanolamine In dichloromethane at 0℃; for 1h;
85%
4-(hydroxymethyl)tetrathiafulvalene
68128-93-8

4-(hydroxymethyl)tetrathiafulvalene

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

bis(tetrathiafulvalen-4-ylmethyl) 4,4'-oxybis(benzenecarboxylate)
177355-71-4

bis(tetrathiafulvalen-4-ylmethyl) 4,4'-oxybis(benzenecarboxylate)

Conditions
ConditionsYield
With dmap In dichloromethane at 20℃; for 18h;84%
In dichloromethane at 20℃; for 18h;73%
10-Undecen-1-ol
112-43-6

10-Undecen-1-ol

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

C36H50O5

C36H50O5

Conditions
ConditionsYield
With pyridine In dichloromethane at 0 - 20℃; for 24h; Inert atmosphere;83%
4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

2-amino-4-nitro-N1-phenylaniline
55315-12-3

2-amino-4-nitro-N1-phenylaniline

2,2'-(4,4'-oxybiphenyl)bis(1-phenyl-5-nitrobenzimidazole)

2,2'-(4,4'-oxybiphenyl)bis(1-phenyl-5-nitrobenzimidazole)

Conditions
ConditionsYield
Stage #1: 4,4'-bis(chlorocarbonyl)diphenyl oxide; 2-amino-4-nitro-N1-phenylaniline With triethylamine In tetrahydrofuran at 5℃; for 18h;
Stage #2: With 4-butanolide; toluene-4-sulfonic acid at 200℃; for 4h;
81.5%
6-hydroxyhexyl methacrylate
13092-57-4

6-hydroxyhexyl methacrylate

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

C34H42O9

C34H42O9

Conditions
ConditionsYield
With dmap; 2,6-di-tert-butyl-4-methyl-phenol; triethylamine In dichloromethane at 20℃; for 2h;78%
With dmap; 2,6-di-tert-butyl-4-methyl-phenol; triethylamine In dichloromethane at 20℃; for 2h;78%
5-Hexen-1-ol
821-41-0

5-Hexen-1-ol

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

C26H30O5

C26H30O5

Conditions
ConditionsYield
With pyridine In dichloromethane at 0 - 20℃; for 24h; Inert atmosphere;78%
2-methyl-2-propenoic acid 2-hydroxyethyl ester
868-77-9

2-methyl-2-propenoic acid 2-hydroxyethyl ester

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

C26H26O9

C26H26O9

Conditions
ConditionsYield
With dmap; 2,6-di-tert-butyl-4-methyl-phenol; triethylamine In dichloromethane at -78℃; for 5h;76%
With dmap; 2,6-di-tert-butyl-4-methyl-phenol; triethylamine In dichloromethane at -78℃; for 5h;76%
With dmap; 2,6-di-tert-butyl-4-methyl-phenol; triethylamine In dichloromethane at -78℃; for 5h;76%
2-methylacrylic acid 3-hydroxypropyl ester
2761-09-3

2-methylacrylic acid 3-hydroxypropyl ester

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

C28H30O9

C28H30O9

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane at 20℃; for 1h;76%
With dmap; 2,6-di-tert-butyl-4-methyl-phenol; triethylamine In dichloromethane at 20℃; for 2h;76%
4-methacryloyloxybutyl alcohol
997-46-6

4-methacryloyloxybutyl alcohol

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

C30H34O9

C30H34O9

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane for 1h;76%
With dmap; 2,6-di-tert-butyl-4-methyl-phenol; triethylamine In dichloromethane at 20℃; for 2h;76%
methylhydrazine
60-34-4

methylhydrazine

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

N,N'-dimethyldihydrazide of p,p'-diphenyl oxide dicarboxylic acid

N,N'-dimethyldihydrazide of p,p'-diphenyl oxide dicarboxylic acid

Conditions
ConditionsYield
In benzene75%
2-Hydroxybenzoylhydrazine
936-02-7

2-Hydroxybenzoylhydrazine

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

4,4'-oxybis(N'-(2-hydroxybenzoyl)benzohydrazide)

4,4'-oxybis(N'-(2-hydroxybenzoyl)benzohydrazide)

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran; N,N-dimethyl-formamide at 90℃; for 9h; Cooling with ice;75%
With triethylamine In N,N-dimethyl-formamide at 90℃; for 9h;
homoalylic alcohol
627-27-0

homoalylic alcohol

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

C22H22O5

C22H22O5

Conditions
ConditionsYield
With pyridine In dichloromethane at 0 - 20℃; for 24h; Inert atmosphere;75%
1-amino-2-propene
107-11-9

1-amino-2-propene

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

N,N'-diallyl-[4,4'-oxybis(benzyl amide)]

N,N'-diallyl-[4,4'-oxybis(benzyl amide)]

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 20℃; for 2h;71%
1,2,4-Triazole
288-88-0

1,2,4-Triazole

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

4,4'-biphenyletherdicarbonyl ditriazole

4,4'-biphenyletherdicarbonyl ditriazole

Conditions
ConditionsYield
In dichloromethane; N,N-dimethyl-formamide for 2.5h;71%
L-alanine methyl ester hydrochloride
2491-20-5

L-alanine methyl ester hydrochloride

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

4,4’-oxybisbenzoyl-bis(L-alanine)

4,4’-oxybisbenzoyl-bis(L-alanine)

Conditions
ConditionsYield
Stage #1: L-alanine methyl ester hydrochloride; 4,4'-bis(chlorocarbonyl)diphenyl oxide With triethylamine In dichloromethane at 20℃; for 6h; Inert atmosphere;
Stage #2: Acidic conditions;
71%
1,2,4-Triazole
288-88-0

1,2,4-Triazole

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

4,4'-biphenyletherdicarbonyl ditriazole

4,4'-biphenyletherdicarbonyl ditriazole

Conditions
ConditionsYield
In dichloromethane; N,N-dimethyl-formamide at 20℃; for 3h;69.4%
pyridin-3-ylamine
462-08-8

pyridin-3-ylamine

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

N,N'-bis(pyridine-3-yl)-4,4'-oxybis(benzoic) dicarboxamide

N,N'-bis(pyridine-3-yl)-4,4'-oxybis(benzoic) dicarboxamide

Conditions
ConditionsYield
Stage #1: pyridin-3-ylamine; 4,4'-bis(chlorocarbonyl)diphenyl oxide In acetonitrile at 80℃;
Stage #2: With triethylamine In methanol at 20℃;
67%
1H-imidazole
288-32-4

1H-imidazole

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

4,4'-biphenyletherdicarbonyl diimidazole

4,4'-biphenyletherdicarbonyl diimidazole

Conditions
ConditionsYield
In tetrahydrofuran at 20℃; for 3.5h; Inert atmosphere;66%
L-proline methyl ester monohydrochloride
2133-40-6

L-proline methyl ester monohydrochloride

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

4,4’-oxybisbenzoyl-bis(L-proline)

4,4’-oxybisbenzoyl-bis(L-proline)

Conditions
ConditionsYield
Stage #1: L-proline methyl ester monohydrochloride; 4,4'-bis(chlorocarbonyl)diphenyl oxide With triethylamine In dichloromethane at 20℃; for 6h; Inert atmosphere;
Stage #2: Acidic conditions;
65%
ethylene glycol
107-21-1

ethylene glycol

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

4,4'-bis(2-hydroxyethoxycarbonyl)diphenyl ether

4,4'-bis(2-hydroxyethoxycarbonyl)diphenyl ether

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane at 0℃; for 3h;60%
With dmap; triethylamine In dichloromethane for 3h;60%
With dmap; triethylamine In dichloromethane at 0℃; for 2h;60%
With dmap; triethylamine; N,N-dimethyl-formamide In dichloromethane at 0℃; for 3h;60%
With dmap; triethylamine In dichloromethane at 0℃; for 3h;60%
4-aminopyridine
504-24-5

4-aminopyridine

4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

4,4′-oxybis(N-(pyridine-4-yl)-benzamide)

4,4′-oxybis(N-(pyridine-4-yl)-benzamide)

Conditions
ConditionsYield
In tetrahydrofuran; dichloromethane at 60℃; Reflux;55%
4,4'-bis(chlorocarbonyl)diphenyl oxide
7158-32-9

4,4'-bis(chlorocarbonyl)diphenyl oxide

5-Hydroxy-isophthalic acid di[2,2']bi[[1,3]dithiolylidene]-4-ylmethyl ester
165196-56-5

5-Hydroxy-isophthalic acid di[2,2']bi[[1,3]dithiolylidene]-4-ylmethyl ester

bis[3,5-bis(tetrathiafulvalen-4-ylmethoxycarbonyl)phenyl] 4,4'-oxydibenzoate

bis[3,5-bis(tetrathiafulvalen-4-ylmethoxycarbonyl)phenyl] 4,4'-oxydibenzoate

Conditions
ConditionsYield
With dmap In dichloromethane at 20℃; for 18h;52%

7158-32-9Relevant articles and documents

Synthesis and characterization of liquid crystalline polyester/graphene and a study of their properties

Hu, Wu-Quan,Zhu, Zong-Zhen,Jin, Jun,Dong, Zheng-Ping,Zhong, Xing,Zhou, Jing-Hui,Da, Shi-Jun,Li, Rong

, p. 2477 - 2483 (2012)

A new rod-like thermotropic liquid crystalline polyester (TLCP) material and its nanocomposites based on different concentrations of graphene were synthesized by in-situ high-temperature solution polymerization. The resulting nanocomposites were characterized using XRD, microscopic analysis (POM, SEM, and TEM), spectroscopic analysis (FT-IR, UV-Vis, and fluorescence), and thermal analysis (TGA and DSC). The XRD and POM methods showed that the composite materials exhibited only the nematic phase. The TEM images revealed that the graphene were distributed in the polymer with sizes ranging from 100 to 200 nm. The absorption spectroscopy data showed that the electronic properties of graphene were mostly retained without damaging their two-dimensional electronic properties, together with the analysis of the maximum absorption spectrum and concentration of the composites in terms of the Lambert-Beer law. The fluorescence from the TLCP moiety was almost completely quenched and red shifted by graphene, indicating that the linkage mode facilitated effective energy and electron transfer between the rod-like TLCP and the extended .-system of graphene. Therefore, this novel nanocomposite material exhibits excellent thermal properties based on the thermogravimetric analysis. Copyright

Zn(ii) and Cd(ii) coordination polymers with a new angular bis-pyridyl-bis-amide: Synthesis, structures and sensing properties

Chen, Jhy-Der,Hu, Ji-Hong,Lee, Wei-Te,Yang, Xiang-Kai

, p. 4486 - 4493 (2021/07/06)

Zn(II) and Cd(II) coordination polymers constructed from a new angular bis-pyridyl-bis-amide ligand and naphthalene-1,4-dicarboxylic acid (1,4-H2NDC), {[Zn2(L)(1,4-NDC)2]·2H2O} [L = 4,4′-oxybis(N-(pyridin-3-ylmethyl)benzamide)], 1, and {[Cd2(L)(1,4-NDC)2]·EtOH}, 2, have been solvothermally synthesized and structurally characterized by using single-crystal X-ray diffraction. While complex 1 displays a 2D double layer with the rare (46·64)-5 L4 topology, complex 2 shows a 3D framework with a new (4·5·6)(45·55·69·7·8) topology. Both complexes 1 and 2 display luminescence properties and 2 exhibits a high sensitivity toward the detection of Fe3+ ions with a Ksv value of 1.9 × 104 M-1. The quenching effect can most probably be ascribed to the interactions between the metal ions and the amide carbonyl oxygen atoms.

(octylphenol polyoxyethylene ether disubstituted) dicarboxylic diphenyl ether nonionic gemini surfactant and synthesis thereof

-

Paragraph 0053; 0054, (2019/05/08)

The invention discloses an (octylphenol polyoxyethylene ether disubstituted) dicarboxylic diphenyl ether nonionic gemini surfactant and synthesis thereof. The (octylphenol polyoxyethylene ether disubstituted) dicarboxylic diphenyl ether nonionic gemini surfactant adopts a structural formula as follows: FORMULA, and is prepared through a two-step reaction as follows: S1, performing an acyl chlorination reaction on 4,4'-dicarboxylic diphenyl ether to obtain 4,4'-diformyl chloride diphenyl ether; S2, performing an esterification reaction on the 4,4'-diformyl chloride diphenyl ether and octylphenol polyoxyethylene ether (OP-10) to obtain a target product (octylphenol polyoxyethylene ether disubstituted) dicarboxylic diphenyl ether. The surfactant is expected to be applied to alkali/surfactantand polymer/surfactant binary compound flooding fluids and an alkali/surfactant/polymer ternary compound flooding fluid, a microemulsion emulsifier and the like in tertiary oil recovery and can be also compounded with a common surfactant to reduce the using cost, so that a condition is created for scale application thereof.

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