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121-65-3

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121-65-3 Usage

Chemical Properties

off-white powder

Uses

4-Dodecylbenzenesulfonic acid (p-dodecylbenzenesulfonic acid, DBSA) may be used:As a solvent for the synthesis of 2-(1,5-diaryl-1,4-pentadien-3-ylidene)-hydrazinecarboximidamide hydrochlorides.In situ coating of rutile nanoparticles.As a stabilizer in the preparation of colloidal CdS.In the fabrication of solid-state dye-sensitized solar cells (DSSCs).

General Description

4-Dodecylbenzenesulfonic acid (DBSA) is an alkyl sulfonate. It participates in the preparation of a polymer along with polystyrene-block-poly(4-vinylpyridine) and a comb-coil A-block-(B-graft-C) type of copolymer.

Check Digit Verification of cas no

The CAS Registry Mumber 121-65-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 121-65:
(5*1)+(4*2)+(3*1)+(2*6)+(1*5)=33
33 % 10 = 3
So 121-65-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H30O3S/c1-2-3-4-5-6-7-8-9-10-11-12-17-13-15-18(16-14-17)22(19,20)21/h13-16H,2-12H2,1H3,(H,19,20,21)

121-65-3 Well-known Company Product Price

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  • Aldrich

  • (44198)  4-Dodecylbenzenesulfonicacid  mixture of isomers, ≥95%

  • 121-65-3

  • 44198-250ML

  • 526.50CNY

  • Detail
  • Aldrich

  • (44198)  4-Dodecylbenzenesulfonicacid  mixture of isomers, ≥95%

  • 121-65-3

  • 44198-1L

  • 1,862.64CNY

  • Detail

121-65-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Dodecylbenzenesulfonic acid

1.2 Other means of identification

Product number -
Other names 4-Dodecylbenzenesulfonic acid

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:121-65-3 SDS

121-65-3Synthetic route

1-dodecylbenzene
123-01-3

1-dodecylbenzene

para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

Conditions
ConditionsYield
With sulfuric acid; sulfur trioxide
With sulfuric acid; sulfur trioxide
With sulfuric acid at 55℃; for 2h; Yield given;
With chlorosulfonic acid In 1,2-dichloro-ethane at 20℃;
With sulfur dioxide; sulfur trioxide
1-dodecylbenzene
123-01-3

1-dodecylbenzene

A

para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

B

dodecylbenzene-sulphonic acid
47221-31-8

dodecylbenzene-sulphonic acid

Conditions
ConditionsYield
With chlorosulfonic acid
With sulfuric acid; sulfur trioxide
4-dodecyl-benzenesulfinic acid
77978-37-1

4-dodecyl-benzenesulfinic acid

para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

Conditions
ConditionsYield
With sodium permanganate
sodium-<4-lauroyl-benzenesulfonate >

sodium-<4-lauroyl-benzenesulfonate >

para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

Conditions
ConditionsYield
With hydrogenchloride; acetic acid; zinc
dodecanophenone
1674-38-0

dodecanophenone

para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: hydrazine hydrate; potassium hydroxide; triethylene glycol / 135 °C
2: H2SO4; SO3
View Scheme
Multi-step reaction with 2 steps
1: amalgamated zinc; aqueous HCl
2: sulfuric acid; SO3
View Scheme
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

neramexane
219810-59-0

neramexane

neramexane 4-dodecylbenzene sulfonate

neramexane 4-dodecylbenzene sulfonate

Conditions
ConditionsYield
at 20℃; Cooling;100%
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

chlormequat chloride
999-81-5

chlormequat chloride

2-chloroethyltrimethylammonium dodecylbenzenesulfonate
156022-53-6

2-chloroethyltrimethylammonium dodecylbenzenesulfonate

Conditions
ConditionsYield
In water at 20℃; for 3h;96%
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

ethylenediamine
107-15-3

ethylenediamine

C20H36N2O2S

C20H36N2O2S

Conditions
ConditionsYield
With pyridine for 2h; Reflux;94%
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

1,4-diaminobutane
110-60-1

1,4-diaminobutane

C22H40N2O2S

C22H40N2O2S

Conditions
ConditionsYield
With pyridine for 2h; Reflux;93%
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

p-dodecylbenzenethiol
20025-90-5

p-dodecylbenzenethiol

Conditions
ConditionsYield
With iodine; triphenylphosphine92%
1,6-Hexanediamine
124-09-4

1,6-Hexanediamine

para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

C24H44N2O2S

C24H44N2O2S

Conditions
ConditionsYield
With pyridine for 2h; Reflux;91%
1,8-diaminooctan
373-44-4

1,8-diaminooctan

para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

C26H48N2O2S

C26H48N2O2S

Conditions
ConditionsYield
With pyridine for 2h; Reflux;90%
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

2-Chloroaniline
95-51-2

2-Chloroaniline

C18H29O3S(1-)*C6H4ClN2(1+)

C18H29O3S(1-)*C6H4ClN2(1+)

Conditions
ConditionsYield
With tert.-butylnitrite In diethyl ether at 20℃; for 0.0666667h; Darkness;90%
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

4-nitro-aniline
100-01-6

4-nitro-aniline

C18H29O3S(1-)*C6H4N3O2(1+)

C18H29O3S(1-)*C6H4N3O2(1+)

Conditions
ConditionsYield
With tert.-butylnitrite In diethyl ether at 20℃; for 0.15h; Darkness;90%
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

1-dodecyl-4-iodobenzene
170698-90-5

1-dodecyl-4-iodobenzene

Conditions
ConditionsYield
Stage #1: para-dodecylbenzenesulfonic acid With 2-Iodobenzoic acid; 3-chloro-benzenecarboperoxoic acid In acetonitrile at 20℃;
Stage #2: With iodine In acetonitrile for 8h; Darkness; Reflux;
88%
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

2-nitro-aniline
88-74-4

2-nitro-aniline

C18H29O3S(1-)*C6H4N3O2(1+)

C18H29O3S(1-)*C6H4N3O2(1+)

Conditions
ConditionsYield
With tert.-butylnitrite In diethyl ether at 20℃; for 0.1h; Darkness;85%
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

3-nitro-aniline
99-09-2

3-nitro-aniline

C18H29O3S(1-)*C6H4N3O2(1+)

C18H29O3S(1-)*C6H4N3O2(1+)

Conditions
ConditionsYield
With tert.-butylnitrite In diethyl ether at 20℃; for 0.25h; Darkness;80%
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

4-methoxy-aniline
104-94-9

4-methoxy-aniline

C18H29O3S(1-)*C7H7N2O(1+)

C18H29O3S(1-)*C7H7N2O(1+)

Conditions
ConditionsYield
With tert.-butylnitrite In diethyl ether at 20℃; for 0.216667h; Darkness;73%
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

4-bromo-aniline
106-40-1

4-bromo-aniline

C18H29O3S(1-)*C6H4BrN2(1+)

C18H29O3S(1-)*C6H4BrN2(1+)

Conditions
ConditionsYield
With tert.-butylnitrite In diethyl ether at 20℃; for 0.25h; Darkness;67%
1-diazopentan-2-one
39910-26-4

1-diazopentan-2-one

para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

4-Dodecyl-benzenesulfonic acid 2-oxo-pentyl ester
80506-58-7

4-Dodecyl-benzenesulfonic acid 2-oxo-pentyl ester

Conditions
ConditionsYield
In diethyl ether Ambient temperature;61%
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

o-toluidine
95-53-4

o-toluidine

C18H29O3S(1-)*C7H7N2(1+)

C18H29O3S(1-)*C7H7N2(1+)

Conditions
ConditionsYield
With tert.-butylnitrite In diethyl ether at 20℃; for 0.216667h; Darkness;58%
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

aniline
62-53-3

aniline

C18H29O3S(1-)*C6H5N2(1+)

C18H29O3S(1-)*C6H5N2(1+)

Conditions
ConditionsYield
With tert.-butylnitrite In diethyl ether at 20℃; for 0.2h; Darkness;56%
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

4-methoxycarbonyl aniline
619-45-4

4-methoxycarbonyl aniline

C18H29O3S(1-)*C8H7N2O2(1+)

C18H29O3S(1-)*C8H7N2O2(1+)

Conditions
ConditionsYield
With tert.-butylnitrite In diethyl ether at 20℃; for 0.116667h; Darkness;47%
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

2-bromo-4-nitroaniline
13296-94-1

2-bromo-4-nitroaniline

C18H29O3S(1-)*C6H3BrN3O2(1+)

C18H29O3S(1-)*C6H3BrN3O2(1+)

Conditions
ConditionsYield
With tert.-butylnitrite In diethyl ether at 20℃; for 0.15h; Darkness;42%
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

Phenyl glycidyl ether
122-60-1

Phenyl glycidyl ether

2-hydroxy-3-phenoxypropyl p-dodecylbenzenesulfonate

2-hydroxy-3-phenoxypropyl p-dodecylbenzenesulfonate

Conditions
ConditionsYield
With 1,4-dioxane at 15.3℃; Rate constant; Kinetics; Mechanism; energy data, ΔH(excit.), ΔS(excit.), Ea, var. temp.;
With water In 1,4-dioxane at 19.9℃; Mechanism; Kinetics; inhibiting effect of water;
With 1,4-dioxane Ambient temperature;
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

guanidine hydrochloride
50-01-1

guanidine hydrochloride

guanidinium 4-dodecylbenzenesulfonate

guanidinium 4-dodecylbenzenesulfonate

Conditions
ConditionsYield
Stage #1: para-dodecylbenzenesulfonic acid With sodium chloride
Stage #2: guanidine hydrochloride In ethanol Heating; Further stages.;
pyrrole
109-97-7

pyrrole

para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

poly(2-methoxyaniline-5-sulfonate)

poly(2-methoxyaniline-5-sulfonate)

polypyrrole film doped with sulfonated polyaniline

polypyrrole film doped with sulfonated polyaniline

Conditions
ConditionsYield
In water
pyrrole
109-97-7

pyrrole

para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

polypyrrole doped with dodecylbenzene sulfonate

polypyrrole doped with dodecylbenzene sulfonate

Conditions
ConditionsYield
In water
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

aniline
62-53-3

aniline

polyaniline 4-dodecylbenzenesulfonate; monomer(s): aniline; 4-dodecylbenzenesulfonic acid

polyaniline 4-dodecylbenzenesulfonate; monomer(s): aniline; 4-dodecylbenzenesulfonic acid

Conditions
ConditionsYield
With sodium phosphate buffer; dihydrogen peroxide; horseradish peroxidase In water at 25℃; for 4h; pH=4.3;
para-dodecylbenzenesulfonic acid
121-65-3

para-dodecylbenzenesulfonic acid

aniline
62-53-3

aniline

polyemeraldine dodecylbenzenesulfonic acid salt; monomer(s): aniline; dodecylbenzenesulfonic acid

polyemeraldine dodecylbenzenesulfonic acid salt; monomer(s): aniline; dodecylbenzenesulfonic acid

Conditions
ConditionsYield
With ammonium persulfate In water at 23℃;

121-65-3Related news

Chemical oxidative polymerization of DODECYLBENZENESULFONIC ACID (cas 121-65-3) aniline salt in chloroform09/10/2019

Polymerizations of dodecylbenzenesulfonic acid aniline salt (DBSAn) in chloroform using various electron acceptors were studied as a function of polymer yield and conductivity. Dichlorodicyanobenzoquinone (DDQ) is an effective oxidant for the polymerization of DBSAn to yield sufficient amount of...detailed

Efficient synthesis of 2,3-disubstituted-2,3-dihydroquinazolin-4(1H)-ones catalyzed by DODECYLBENZENESULFONIC ACID (cas 121-65-3) in aqueous media under ultrasound irradiation09/09/2019

Synthesis of 2,3-disubstituted-2,3-dihydroquinazolin-4(1H)-one derivatives catalyzed by dodecylbenzenesulfonic acid was carried out in 80–92% yields at 40–42 °C within 1–2 h in aqueous media via one-pot three-component condensation of isatoic anhydride, aromatic aldehyde and amine under ultr...detailed

Structure–property relationship of DODECYLBENZENESULFONIC ACID (cas 121-65-3) doped polypyrrole09/08/2019

Dodecylbenzenesulfonic acid (DBSA) doped polypyrroles (PPys) were chemically synthesized in different polymerization times and molar ratios of pyrrole (Py) to DBSA feed. The microstructures of these PPys were investigated by X-ray diffraction (XRD) and Fourier Transform Infrared (FTIR). UV–vis ...detailed

Effect of DODECYLBENZENESULFONIC ACID (cas 121-65-3) as a Surfactant on the Properties of Polyaniline/Graphene Nanocomposites09/04/2019

Polyaniline (PANI) is the most studied conducting polymer because of its conductivity, environmental stability and ease of preparation. This paper reports on the fabrication of PANI by using interfacial polymerisation method. Dodecylbenzenesulfonic acid (DBSA) was used as a surfactant in the syn...detailed

121-65-3Relevant articles and documents

Petroleum waste as raw materials for production of electricity by Photogalvanic solar cell

Bendary, Samar H.,El-Tabei, A. S.,Mahmoud, Sawsan A.

, (2021)

Petroleum industry produces a bulky rate of harmful environmental wastes. Recycling of these wastes to produce added value products is of prim importance. In this work, Synthesis of sodium 4-dodecyl benzene sulfonate (SDBS) anionic surfactant from petroleum waste was done through two steps method. The composition of the produced anionic surfactant was investigated by using FTIR, 1HNMR, and 13CNMR spectra techniques. Anionic surfactant was applied in photogalvanic cell (PGC) for production of electricity. PGC can be described as an electrochemical cell where the change in both voltage and current arises from the generated photochemical changes in the reactants during the oxidation–reduction reaction in the cell. the recorded electrical cell performance are; maximum power (PPP) 39.8μW, short circuit current (iSC)145.2 μA, open circuit potential (VOC) 490 mV, fill factor (FF) 0.65, conversion efficiency (η) 0.77%, and storage capacity t0.565 min for system containing Tris (2,2′-bipyrdyl) Ruthenium (II) chloride hexahydrate (TBRC) as photosensitize, Oxalic acid (OX) as reductant, and (SDBS) as anionic surfactant under artificial illumination. The cell performance is optimized and the preliminary mechanism for the solar energy conversion in PGC is also proposed.

PROPRIETES PHYSICI-CHIMIQUES DE N-ALKYL P-BENZENE SULFONATES ALCALINS: TEMPERATURE DE KRAFFT ET CONCENTRATION CRITIQUE MICELLAIRE

Rouviere, Jacques,Faucompre, Bernard,Lindheimer, Marc,Partyka, Stanislas,Brun, Bernard

, p. 309 - 314 (2007/10/02)

The Krafft points (Tk) and the critical micellar concentrations (c.m.c.) on the alkali salts of n-alkyl-p-benzene sulfonates have been measured by solubility and conductivity experiments.For the sodium compounds, we observe a linear relationship between log10cmc and n the number of carbon atoms in the alkyl chain of the surfactant, a linear relationship between the Tk of the homologous surfactants studied and n.The substitution of sodium counter-ion by another alkali, decreases the Krafft point which seems to be correlated to the hydratation of the counter-ion.These data permit us to know the Tk and c.m.c. of homologous series of various amphiphiles.By treating the formation of micelles as analogous to phase separation, the determination of the variation of c.m.c. with temperature has been studied, these results have been converted into, enthalpy and free energy of micellization and these have been compared with corresponding values obtained from literature data.

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