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335-64-8 Usage

Uses

Different sources of media describe the Uses of 335-64-8 differently. You can refer to the following data:
1. Perfluorooctanoyl chloride is derivatizated and used in the determination of Amphetamine and Methamphetamine in Blood. It can be used in agrochemical, pharmaceutical and dyestuff field .
2. Pentadecafluorooctanoyl chloride can be used:In the derivatization of poly(2-hydroxyethyl methacrylate) (PHEMA) via esterification for use as composite membranes.In the fabrication of superhydrophobic cellulose surfaces.As a reagent for the esterification of hydroxyl-functionalized gold nanocrystals.As a reagent in the synthesis of fluorous derivatives of diaminocyclohexane which are used as ligands.

Check Digit Verification of cas no

The CAS Registry Mumber 335-64-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 335-64:
(5*3)+(4*3)+(3*5)+(2*6)+(1*4)=58
58 % 10 = 8
So 335-64-8 is a valid CAS Registry Number.
InChI:InChI=1/C8ClF15O/c9-1(25)2(10,11)3(12,13)4(14,15)5(16,17)6(18,19)7(20,21)8(22,23)24

335-64-8 Well-known Company Product Price

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  • Detail
  • Alfa Aesar

  • (L09294)  Perfluorooctanoyl chloride, 97%   

  • 335-64-8

  • 5g

  • 387.0CNY

  • Detail
  • Alfa Aesar

  • (L09294)  Perfluorooctanoyl chloride, 97%   

  • 335-64-8

  • 25g

  • 1755.0CNY

  • Detail
  • Aldrich

  • (290904)  Pentadecafluorooctanoylchloride  97%

  • 335-64-8

  • 290904-5G

  • 537.03CNY

  • Detail
  • Aldrich

  • (290904)  Pentadecafluorooctanoylchloride  97%

  • 335-64-8

  • 290904-25G

  • 1,826.37CNY

  • Detail

335-64-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctanoyl chloride

1.2 Other means of identification

Product number -
Other names pentadecafluorooctanoic acid chloride

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:335-64-8 SDS

335-64-8Synthetic route

Perfluorooctanoic acid
335-67-1

Perfluorooctanoic acid

pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

Conditions
ConditionsYield
With pyridine; thionyl chloride at 80℃; for 4h; Reflux;97%
With thionyl chloride; N,N-dimethyl-formamide for 4h; Heating;90%
With benzoyl chloride Heating;77%
methyl perfluorooctanoate
376-27-2

methyl perfluorooctanoate

pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

Conditions
ConditionsYield
With chlorine Irradiation;
sodium perfluorooctanoate
335-95-5

sodium perfluorooctanoate

pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

Conditions
ConditionsYield
With Phthaloyl dichloride
perfluorooctyl sulfofluorure
307-35-7

perfluorooctyl sulfofluorure

A

Perfluorooctane
307-34-6

Perfluorooctane

B

1-Chloroperfluorooctane
307-33-5

1-Chloroperfluorooctane

C

pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

D

perfluorooctanesulphonyl chloride
423-60-9

perfluorooctanesulphonyl chloride

Conditions
ConditionsYield
With aluminium trichloride at 100 - 110℃; for 5h; Title compound not separated from byproducts;
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

(trimethylsilyl)diphenylphosphine
17154-34-6

(trimethylsilyl)diphenylphosphine

diphenyl-perfluoro-octanoylphosphine
548459-25-2

diphenyl-perfluoro-octanoylphosphine

Conditions
ConditionsYield
In tetrahydrofuran at 0℃; for 1h;100%
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

diphenylphosphane
829-85-6

diphenylphosphane

diphenyl-perfluoro-octanoylphosphine
548459-25-2

diphenyl-perfluoro-octanoylphosphine

Conditions
ConditionsYield
With triethylamine100%
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

Perfluorooctanoic acid
335-67-1

Perfluorooctanoic acid

Conditions
ConditionsYield
With water99.6%
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

L-valine methylester hydrochloride
6306-52-1

L-valine methylester hydrochloride

(S)-N-pentadecafluorooctanoylvalinemethylester
170980-91-3

(S)-N-pentadecafluorooctanoylvalinemethylester

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃; for 3.5h;99%
1-hydroxy-2(1H)-pyridinethione
1121-30-8

1-hydroxy-2(1H)-pyridinethione

2,2,3,3,3-pentafluoropropanoic anhydride
356-42-3

2,2,3,3,3-pentafluoropropanoic anhydride

pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

trifluoroacetic anhydride
407-25-0

trifluoroacetic anhydride

heptafluorobutyric anhydride
336-59-4

heptafluorobutyric anhydride

A

2-((trifluoromethyl)thio)pyridine
57830-49-6

2-((trifluoromethyl)thio)pyridine

B

2-pyridyl pentafluoroethyl sulfide
107146-03-2

2-pyridyl pentafluoroethyl sulfide

C

2-(perfluoro-n-buthylthio)-pyridine
107146-04-3

2-(perfluoro-n-buthylthio)-pyridine

D

2-(perfluoroheptylthio)-pyridine
107146-05-4

2-(perfluoroheptylthio)-pyridine

Conditions
ConditionsYield
Product distribution; Irradiation; further reactions inpresence of perfluorobutyric anhydride with different alkenes;A 98%
B 94%
C 95%
D 60%
N-Boc-N'-(pyren-1-ylmethyl)-3,6-dioxaoctane-1,8-diamine
904684-59-9

N-Boc-N'-(pyren-1-ylmethyl)-3,6-dioxaoctane-1,8-diamine

pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

N'-2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctanoyl-N-Boc-N'-(pyren-1-ylmethyl)-3,6-dioxaoctane-1,8-diamide
904684-62-4

N'-2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctanoyl-N-Boc-N'-(pyren-1-ylmethyl)-3,6-dioxaoctane-1,8-diamide

Conditions
ConditionsYield
With pyridine; dmap In dichloromethane at 20℃; for 3h;97%
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

2,3,4,6-tetra-O-pivaloyl-d-galactopyranosylamine
1228010-31-8

2,3,4,6-tetra-O-pivaloyl-d-galactopyranosylamine

C34H44F15NO10
1228010-32-9

C34H44F15NO10

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 0 - 22℃; for 19.75h;96%
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

2-aminomethyl-15-crown-5
83585-56-2

2-aminomethyl-15-crown-5

N-(1,4,7,10,13-pentaoxacyclopentadecan-2-ylmethyl)-2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctanamide
1228010-22-7

N-(1,4,7,10,13-pentaoxacyclopentadecan-2-ylmethyl)-2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctanamide

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 0 - 22℃; for 19.75h;96%
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

1-amino-3-(dimethylamino)propane
109-55-7

1-amino-3-(dimethylamino)propane

2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctanoic acid [3-(dimethylamino)propyl]amide
376-23-8

2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctanoic acid [3-(dimethylamino)propyl]amide

Conditions
ConditionsYield
In tetrahydrofuran at -5 - 20℃; for 5h;95.9%
isatoic anhydride
118-48-9

isatoic anhydride

pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

2-pentadecafluoroheptyl-benzo[d][1,3]oxazin-4-one
16062-72-9

2-pentadecafluoroheptyl-benzo[d][1,3]oxazin-4-one

Conditions
ConditionsYield
With pyridine at 75℃; for 2h;95%
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

2-Hydroxy-4-methylanilin
2835-98-5

2-Hydroxy-4-methylanilin

2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-Pentadecafluoro-octanoic acid (2-hydroxy-4-methyl-phenyl)-amide

2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-Pentadecafluoro-octanoic acid (2-hydroxy-4-methyl-phenyl)-amide

Conditions
ConditionsYield
In pyridine at 40℃; for 0.5h;95%
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

perfluorooctanoyl ammonia
423-54-1

perfluorooctanoyl ammonia

Conditions
ConditionsYield
With ammonia; calcium oxide In ethanol at 15℃; for 4h;94%
With ammonia In diethyl ether
With ammonia; calcium oxide In ethanol for 4h; Inert atmosphere;
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

(1R,2R)-1,2-diaminocyclohexane
20439-47-8

(1R,2R)-1,2-diaminocyclohexane

R,R-N,N'-diperfluorooctanoyl-1,2-diaminocyclohexane

R,R-N,N'-diperfluorooctanoyl-1,2-diaminocyclohexane

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 0 - 20℃; Inert atmosphere;94%
With triethylamine In tetrahydrofuran at 0 - 20℃;88%
With triethylamine In tetrahydrofuran at 0℃; for 1h;
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

Bis(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-Heptadecafluoro-undecyl)amine

Bis(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-Heptadecafluoro-undecyl)amine

N,N-bis[3-(perfluorooctyl)propyl]perfluorooctanamide

N,N-bis[3-(perfluorooctyl)propyl]perfluorooctanamide

Conditions
ConditionsYield
With triethylamine In diethyl ether at 20℃; for 1h;94%
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

1,4,7,10-tetraoxa-15-azacyclopentadecane
66943-05-3

1,4,7,10-tetraoxa-15-azacyclopentadecane

N-perfluorooctanoyl aza-15-crown-5

N-perfluorooctanoyl aza-15-crown-5

Conditions
ConditionsYield
With triethylamine In acetonitrile at 0 - 20℃; Acylation;92%
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

sym-(amino)dibenzo-16-crown-5
241490-98-2

sym-(amino)dibenzo-16-crown-5

N-(sym-dibenzo-16-crown-5)-perfluorooctanoyl amide

N-(sym-dibenzo-16-crown-5)-perfluorooctanoyl amide

Conditions
ConditionsYield
With triethylamine In acetonitrile at 20℃; for 12h;92%
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

perfluorooctanoyl ammonia
423-54-1

perfluorooctanoyl ammonia

N,N-bis(perfluorooctyl)imine

N,N-bis(perfluorooctyl)imine

Conditions
ConditionsYield
With pyridine In ethanol at 5℃; for 8h;92%
With triethylamine In ethanol at 5℃; for 6h;
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

2-bromoethylamine hydrobromide
2576-47-8

2-bromoethylamine hydrobromide

N-(2-bromoethyl)perfluoroctanamide
110388-00-6

N-(2-bromoethyl)perfluoroctanamide

Conditions
ConditionsYield
With zinc(II) oxide In acetonitrile Heating;91%
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

4-(4-chlorophenyl)butan-2-ol
76019-94-8

4-(4-chlorophenyl)butan-2-ol

1-(4-chlorophenyl)but-3-yl perfluorooctanoate

1-(4-chlorophenyl)but-3-yl perfluorooctanoate

Conditions
ConditionsYield
With pyridine In dichloromethane at 0 - 20℃; for 2h; Inert atmosphere;91%
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

4-amino-6-methyl-benzene-1,3-disulfonic acid diamide
1020-33-3

4-amino-6-methyl-benzene-1,3-disulfonic acid diamide

2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-Pentadecafluoro-octanoic acid (5-methyl-2,4-disulfamoyl-phenyl)-amide

2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-Pentadecafluoro-octanoic acid (5-methyl-2,4-disulfamoyl-phenyl)-amide

Conditions
ConditionsYield
In 1,4-dioxane Heating;90%
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

Tributyl-[fluoro-(tributyl-λ5-phosphanylidene)-methyl]-phosphonium; chloride
84195-43-7

Tributyl-[fluoro-(tributyl-λ5-phosphanylidene)-methyl]-phosphonium; chloride

C21H27F16OP

C21H27F16OP

Conditions
ConditionsYield
at 0 - 20℃; for 1h;90%
trimethylsilyl cyanide
7677-24-9

trimethylsilyl cyanide

pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

2-Pentadecafluoroheptyl-2-trimethylsilanyloxy-malononitrile

2-Pentadecafluoroheptyl-2-trimethylsilanyloxy-malononitrile

Conditions
ConditionsYield
tetra-n-butylammonium cyanide for 3h; Ambient temperature;90%
Octanethiol
111-88-6

Octanethiol

pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

n-octyl pentadecafluorothiooctanoate

n-octyl pentadecafluorothiooctanoate

Conditions
ConditionsYield
With dmap In dichloromethane at 0 - 40℃;90%
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

2-(sym-dibenzo-16-crown-5-oxo)ethylamine
220968-09-2

2-(sym-dibenzo-16-crown-5-oxo)ethylamine

N-[(2-sym-dibenzo-16-crown-5-oxy)ethyl] perfluorooctanoyl amide

N-[(2-sym-dibenzo-16-crown-5-oxy)ethyl] perfluorooctanoyl amide

Conditions
ConditionsYield
With triethylamine In acetonitrile at 20℃; for 12h;90%
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

2-(sym-dicyclohexano-16-crown-5-oxy)ethylamine
599171-69-4

2-(sym-dicyclohexano-16-crown-5-oxy)ethylamine

N-[(2-sym-dicyclohexano-16-crown-5-oxy)ethyl] perfluorooctanoyl amide
599171-76-3

N-[(2-sym-dicyclohexano-16-crown-5-oxy)ethyl] perfluorooctanoyl amide

Conditions
ConditionsYield
With triethylamine In acetonitrile at 20℃; for 12h;90%
poly(methyl methacrylate)-b-poly(2-hydroxyethyl methacrylate) block copolymer, block ratio: 26:5 kg/M, Mw = 24500, PDI = 1.05; monomer(s): methyl methacrylate; 2-[(trimethylsilyl)oxy]ethyl methacrylate; sec-butyl lithium; 1,1-diphenylethylene

poly(methyl methacrylate)-b-poly(2-hydroxyethyl methacrylate) block copolymer, block ratio: 26:5 kg/M, Mw = 24500, PDI = 1.05; monomer(s): methyl methacrylate; 2-[(trimethylsilyl)oxy]ethyl methacrylate; sec-butyl lithium; 1,1-diphenylethylene

pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

poly(methyl methacrylate)-b-poly(2-(perfluorooctanoyloxy)ethyl methacrylate) block copolymer, block ratio: 26:19.9 kg/mol, Mw = 29200, PDI = 1.05

poly(methyl methacrylate)-b-poly(2-(perfluorooctanoyloxy)ethyl methacrylate) block copolymer, block ratio: 26:19.9 kg/mol, Mw = 29200, PDI = 1.05

Conditions
ConditionsYield
With pyridine In tetrahydrofuran at 45℃;90%
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

Cholestanol
80-97-7

Cholestanol

5α-cholestan-3β-ol pentadecafluorooctanoate
109481-61-0

5α-cholestan-3β-ol pentadecafluorooctanoate

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane for 2h; Ambient temperature;89.2%
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

N-(pentafluorosulfanylperfluorobutyryl)hydrazine
154023-41-3

N-(pentafluorosulfanylperfluorobutyryl)hydrazine

C12H2F26N2O2S

C12H2F26N2O2S

Conditions
ConditionsYield
With pyridine In diethyl ether at 25℃; for 0.333333h;89%
pentadecafluorooctanoyl chloride
335-64-8

pentadecafluorooctanoyl chloride

4-(4-methoxy-phenyl)-butan-2-ol
67952-38-9

4-(4-methoxy-phenyl)-butan-2-ol

1-(4-methoxyphenyl)but-3-yl perfluorooctanoate

1-(4-methoxyphenyl)but-3-yl perfluorooctanoate

Conditions
ConditionsYield
With pyridine In dichloromethane at 0 - 20℃; for 2h; Inert atmosphere;89%

335-64-8Relevant articles and documents

van Dyke Tiers

, p. 2038 (1964)

Synthesis and characterization of a novel fluorine-containing polymer emulsion with core/shell structure

Gao, Jinzhang,Wang, Xuemei,Wei, Yunxia,Yang, Wu

, p. 282 - 286 (2006)

A novel fluorine-containing polymer emulsion 4 with core/shell structure was synthesized in water phase by a two-stage emulsion polymerization technique using monomer 3 (i.e., 2-methacryloyloxyethyl perfluorooctanoate (MAEF)) reacting with the monomers such as butyl acrylate (BA), acrylic acid (AA) and styrene (ST). The monomer 3 was synthesized from the intermediate 2 (pentadecafluoro-octanoyl chloride) reacting with β-hydroxyethyl methacrylate (HEMA). Polymer film were prepared by coating emulsion 4 directly on a cleaned glass plate and allowed to dry at room temperature. Moreover, the characteristics of polymer film such as hydrophobicity, chemical resistance, surface composition, thermal stability, emulsion particle morphology, as well as the film-forming property were also studied.

Perfluoropolyether ester derivative as well as preparation method and application thereof

-

Paragraph 0041-0046, (2020/06/20)

The invention discloses a perfluoropolyether ester derivative as well as a preparation method and application thereof. The preparation method of the perfluoropolyether ester derivative comprises the following steps: (1) performing acyl chlorination on pentafluorobenzoic acid to obtain pentafluorobenzoyl chloride; and (2) carrying out an esterification reaction on the pentafluorobenzoyl chloride and perfluoropolyether alcohol to obtain the perfluoropolyether ester derivative. In perfluoropolyether derivative molecules provided by the invention, a perfluoropolyether part provides compatibility with perfluoropolyether, and an ester group and a pentafluorophenyl part provide enhanced lubricity and bearing capacity; a large number of fluorine atoms contained in molecules can better generate friction chemical reaction with the metal surface, so that a film structure is easily formed on the surface of a friction pair, and the lubricating effect is promoted. The perfluoropolyether derivative also has good thermal stability and can still keep a certain lubricating effect at 150 DEG C. The perfluoropolyether ester derivative has good antifriction and antiwear properties when used as a lubricating grease additive.

A method of preparing liquid carbon dioxide thickening agent (by machine translation)

-

Paragraph 0020; 0021; 0029; 0030; 0038; 0039, (2019/10/22)

The invention relates to a method for conventional oil and gas reservoir development of thickening agent preparation method of liquid carbon dioxide. It can solve the conventional mining method to the problem of oil-gas reservoir damage, the technical proposal: first to the bottle adding toluene and water, then adding serinol, in 0 °C [...] carbon acid tert-butyl ester, in the 25 °C reaction 4 hours, the distillation get intermediate (1), in the other a bottle after adding perfluroalkyl octoate, in 75 °C by adding thionyl chloride and N, N - dimethyl formamide, reaction 2 hours, distillation get intermediate (2); then in another bottle into the intermediate product in (1), raising the temperature to 75 °C dropping intermediate product (2), in the 75 °C reaction 12 hours to make the intermediate product (3); the final in a bottle by adding methylene chloride and trifluoroacetic acid, then adding the intermediate product (3), in the 25 °C reaction 2 hours, extraction after vacuum drying, adding 1, 6 - has been diisocyanate reaction 2 min to obtain the final product. The thickening agent can increase the viscosity of the carbon dioxide, can be used for fracturing. (by machine translation)

PH-responsive superomniphobic nanoparticles as versatile candidates for encapsulating adhesive liquid marbles

Chandan,Ramakrishna,Sunitha,Chandran, M. Satheesh,Kumar, K. S. Santhosh,Mathew, Dona

, p. 22813 - 22823 (2017/11/14)

Conventional adhesives are rarely used in sophisticated applications such as micro-fluidic devices or 'operations of bonding from a distance' due to their permanent wetting characteristics. Liquid marbles offer exceptional switching between non-wetting and wetting on demand. In this contribution, we present a novel approach to encapsulate both hydrophilic (epoxy resin) and hydrophobic (siloxane polymer) liquids via wrapping them with superomniphobic nanoparticles. The free energy for marble formation is lower for a hydrophobic liquid (0.931 × 10-16 J), whereas a hydrophilic liquid registers a higher value of 1.86 × 10-16 J. The mechanical bursting energy for hydrophobic marbles (20 μJ) is lower than that for their hydrophilic counterpart (48.6 μJ). The static friction coefficients of epoxy-based liquid marble are between 0.015 and 0.020 on glass, aluminium and stainless steel substrates. As a highlight, the nanoparticle coating is responsive to pH, and the bursting time of the liquid marbles can be tuned from 1 minute to several hours. It is demonstrated that the adhesive strength of cross-linked epoxy obtained by a liquid marble route is higher than that obtained vis-a-vis a conventional wetting route. The liquid marbles presented in this work can be ruptured by changing the pH, have a lower friction coefficient compared to the bare liquids (more rolling distance, which is highly essential for bonding of an intricate space from a distance) and are useful as dry adhesives.

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