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Sodium 4-amino-1-naphthalenesulfonate is a grayish white crystalline powder that serves as a versatile chemical compound with various applications across different industries.

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  • 130-13-2 Structure
  • Basic information

    1. Product Name: Sodium 4-amino-1-naphthalenesulfonate
    2. Synonyms: SODIUM NAPHTHIONATE;SODIUM NAPTHIONATE;SODIUM 1-NAPHTHYLAMINE-4-SULFONATE;SODIUM 4-AMINO-1-NAPHTHALENESULFONATE;PARA-NAPHTHIONIC ACID, NA SALT;NAPHTHYLAMINE-4-SULFONIC ACID SODIUM SALT;NAPHTHIONIC ACID SODIUM SALT;NAPHTHIONIC ACID SODIUM SALT 0.5-WATER
    3. CAS NO:130-13-2
    4. Molecular Formula: C10H8NO3S*Na
    5. Molecular Weight: 245.23
    6. EINECS: 204-975-5
    7. Product Categories: Intermediates of Dyes and Pigments
    8. Mol File: 130-13-2.mol
  • Chemical Properties

    1. Melting Point: 280 °C (dec.)(lit.)
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: grayish white crystalline powder
    5. Density: 1.6703
    6. Refractive Index: N/A
    7. Storage Temp.: Store below +30°C.
    8. Solubility: N/A
    9. Merck: 14,6403
    10. CAS DataBase Reference: Sodium 4-amino-1-naphthalenesulfonate(CAS DataBase Reference)
    11. NIST Chemistry Reference: Sodium 4-amino-1-naphthalenesulfonate(130-13-2)
    12. EPA Substance Registry System: Sodium 4-amino-1-naphthalenesulfonate(130-13-2)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26
    4. WGK Germany: 3
    5. RTECS:
    6. F: 3-8-23
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 130-13-2(Hazardous Substances Data)

130-13-2 Usage

Uses

Used in Chemical Industry:
Sodium 4-amino-1-naphthalenesulfonate is used as Riegler's reagent for [application type] nitrous acid [application reason] in the chemical industry, facilitating specific chemical reactions and analysis.
Used in Manufacturing Industry:
In the manufacturing industry, Sodium 4-amino-1-naphthalenesulfonate is used as a key component in the [application type] manufacture of dyestuffs [application reason], contributing to the production of various dyes with desired properties and characteristics.

Preparation

The preparation of Sodium 4-amino-1-naphthalenesulfonate is as follows:To a suspension of 4-amino-l -naphthalene sulfonic acid (10.Og, 44.8 mmol) in 10 ml MeOH was added 5 N NaOMe (9 ml). The mixture was sonicated to effect complete solution. The solvent was evaporated to provide the sodium salt of -amino-1- naphthalene sulfonic acid as a white solid. This solid was suspended in 100 ml acetic anhydride and heated at 110 °C for 2 1/2 h. Adding some MeOH to the cooled mixture and co-evaporating with 3x100 ml toluene gave the Na-salt of 4-acetamidonaphthalene-l -sulfonic acid as a white powder.

Check Digit Verification of cas no

The CAS Registry Mumber 130-13-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,3 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 130-13:
(5*1)+(4*3)+(3*0)+(2*1)+(1*3)=22
22 % 10 = 2
So 130-13-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO3S/c11-9-5-6-10(15(12,13)14)8-4-2-1-3-7(8)9/h1-6H,11H2,(H,12,13,14)/p-1

130-13-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Amino-1-Naphthalenesulfonic Acid Sodium Salt

1.2 Other means of identification

Product number -
Other names Sodium 1-Naphthylamine-4-sulfonate

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:130-13-2 SDS

130-13-2Synthetic route

sodium 4-iodonaphthalene-1-sulfonate

sodium 4-iodonaphthalene-1-sulfonate

sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

Conditions
ConditionsYield
With sodium azide; carbon monoxide; palladium diacetate; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene In water-d2; dimethyl sulfoxide Sealed tube;44.8%
4-amino-1-naphthalenesufonic acid
84-86-6

4-amino-1-naphthalenesufonic acid

sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

Conditions
ConditionsYield
With sodium methylate In methanol
congo red
573-58-0

congo red

A

biphenyl
92-52-4

biphenyl

B

sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

Conditions
ConditionsYield
With sodium tetrahydroborate at 20℃; Kinetics; Reagent/catalyst;
With sodium tetrahydroborate In water Catalytic behavior; Kinetics;
3,3'-((biphenyl)-4,4'-diylbis(azo))bis(4-amino-1-naphthalenesulphonic acid) disodium

3,3'-((biphenyl)-4,4'-diylbis(azo))bis(4-amino-1-naphthalenesulphonic acid) disodium

A

biphenyl
92-52-4

biphenyl

B

sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

Conditions
ConditionsYield
With sodium tetrahydroborate In water at 20℃; Kinetics; Reagent/catalyst; Concentration;
1-amino-naphthalene
134-32-7

1-amino-naphthalene

sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

Conditions
ConditionsYield
Stage #1: 1-amino-naphthalene With sulfur trioxide In 1,2-dichloro-benzene at 40℃; for 0.833333h; Large scale;
Stage #2: With sodium hydroxide In water; 1,2-dichloro-benzene at 85 - 190℃; for 3h; pH=7; Temperature; Solvent; Reagent/catalyst; Autoclave; Large scale;
Brasilamina Congo 4B
573-58-0

Brasilamina Congo 4B

sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

Conditions
ConditionsYield
With sodium tetrahydroborate In water
congo red
573-58-0

congo red

A

sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

B

p,p'-diaminobiphenyl
92-87-5

p,p'-diaminobiphenyl

Conditions
ConditionsYield
With sodium tetrahydroborate In water for 0.0388889h; Kinetics; Time;
sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

sodium 1-naphthol-4-sulfonate
6099-57-6

sodium 1-naphthol-4-sulfonate

Conditions
ConditionsYield
With sodium hydrogensulfite In water for 24h; Heating;90%
sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

p-methoxyphenylazobenzenethiosulfonate
91363-28-9

p-methoxyphenylazobenzenethiosulfonate

2-(4-methoxyphenylazo)-1-aminonaphthalene-4-sulfonic acid
19649-50-4

2-(4-methoxyphenylazo)-1-aminonaphthalene-4-sulfonic acid

Conditions
ConditionsYield
With hydrogenchloride; sodium acetate at 40 - 60℃; for 3h;78%
sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

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

benzene-1,3-dicarbonyl dichloride

disodium 4,4'-[1,3-phenylenebis(carbonylimino)]bis(1-naphthalenesulfonate)

disodium 4,4'-[1,3-phenylenebis(carbonylimino)]bis(1-naphthalenesulfonate)

Conditions
ConditionsYield
With sodium carbonate In chloroform; water at 0 - 25℃; for 23h;60%
lead(II) nitrate

lead(II) nitrate

potassium chloride

potassium chloride

water
7732-18-5

water

sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

[Pb2(μ3-4-amino-1-naphthalenesulfonic acid)2(μ2-Cl)2(H2O)2]n
1621007-92-8

[Pb2(μ3-4-amino-1-naphthalenesulfonic acid)2(μ2-Cl)2(H2O)2]n

Conditions
ConditionsYield
for 3h; Reflux;47%
1,12-dodecanedioyl dichloride
4834-98-4

1,12-dodecanedioyl dichloride

sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

disodium 4,4'-<1,10-decanediylbis(carbonylamino)>bis(1-naphthalenesulfonate)

disodium 4,4'-<1,10-decanediylbis(carbonylamino)>bis(1-naphthalenesulfonate)

Conditions
ConditionsYield
With pyridine at 120 - 125℃; for 4.5h;31%
sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

sodium 4-iodonaphthalene-1-sulfonate

sodium 4-iodonaphthalene-1-sulfonate

Conditions
ConditionsYield
Stage #1: sodium 4-amino-1-naphthalenesulfonate With hydrogenchloride; sodium nitrite In water at 0℃; for 1h;
Stage #2: With sodium iodide In water at 20 - 90℃; for 3.5h;
29.8%
C36H60O30*C35H41N3O2(2+)*2Br(1-)

C36H60O30*C35H41N3O2(2+)*2Br(1-)

sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

C45H47N4O4S(1+)*C36H60O30*2Cl(1-)*Na(1+)

C45H47N4O4S(1+)*C36H60O30*2Cl(1-)*Na(1+)

Conditions
ConditionsYield
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In water at 20℃; for 48h;22%
Diphenyl-4,4'-bis-diazonium
5957-03-9

Diphenyl-4,4'-bis-diazonium

sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

4,4'-bis-[3-acetyl-3-(4-sulfo-[1]naphthyl)-triazenyl]-biphenyl

4,4'-bis-[3-acetyl-3-(4-sulfo-[1]naphthyl)-triazenyl]-biphenyl

Conditions
ConditionsYield
With water
sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

4-acetamidonaphthalene-1-sulfonyl chloride
5690-20-0

4-acetamidonaphthalene-1-sulfonyl chloride

sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

4-acetylamino-8-nitro-naphthalene-1-sulfonic acid

4-acetylamino-8-nitro-naphthalene-1-sulfonic acid

Conditions
ConditionsYield
With sulfuric acid; nitric acid
sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

2-[123I]iodobenzidine dihydrochloride

2-[123I]iodobenzidine dihydrochloride

3,3'-[(2-[123I]iodo-1,1'-biphenyl)-4,4'-diylbis(azo)]bis[4-amino-1-naphthalenesulfonic acid] disodium salt

3,3'-[(2-[123I]iodo-1,1'-biphenyl)-4,4'-diylbis(azo)]bis[4-amino-1-naphthalenesulfonic acid] disodium salt

Conditions
ConditionsYield
With hydrogenchloride; sodium nitrite 2.) 2.5 h; Yield given. Multistep reaction;
sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

N-(4,4'-diamino-biphenyl-2-ylmethyl)-3-{(2-tritylsulfanyl-ethyl)-[(2-tritylsulfanyl-ethylcarbamoyl)-methyl]-amino}-propionamide
199273-21-7

N-(4,4'-diamino-biphenyl-2-ylmethyl)-3-{(2-tritylsulfanyl-ethyl)-[(2-tritylsulfanyl-ethylcarbamoyl)-methyl]-amino}-propionamide

C80H69N9O8S4(2-)*2Na(1+)

C80H69N9O8S4(2-)*2Na(1+)

Conditions
ConditionsYield
With hydrogenchloride; sodium acetate; sodium carbonate; sodium nitrite 1.) THF, 5 deg C, 2 min, 2.) THF, 5 deg C, 1 h; Yield given; Multistep reaction;
water
7732-18-5

water

bromine
7726-95-6

bromine

sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

A

2,4-dibromo-1-naphthylamine
20191-76-8

2,4-dibromo-1-naphthylamine

B

3-bromo-4-amino-naphthalene-sulfonic acid-(1)

3-bromo-4-amino-naphthalene-sulfonic acid-(1)

sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

nitrosylsulfuric acid

nitrosylsulfuric acid

4-nitroso-naphthyl-(1)-amine

4-nitroso-naphthyl-(1)-amine

3,3'-dimethoxy-(1,1'-biphenyl)-4,4'-diamine
119-90-4

3,3'-dimethoxy-(1,1'-biphenyl)-4,4'-diamine

sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

4,4'-diamino-3,3'-(3,3'-dimethoxybiphenyl-4,4'-diyl-bis-azo)-bis-naphthalene-1-sulfonic acid disodium salt

4,4'-diamino-3,3'-(3,3'-dimethoxybiphenyl-4,4'-diyl-bis-azo)-bis-naphthalene-1-sulfonic acid disodium salt

Conditions
ConditionsYield
Stage #1: 3,3'-dimethoxy-(1,1'-biphenyl)-4,4'-diamine With hydrogenchloride; sodium nitrite at 0℃;
Stage #2: sodium 4-amino-1-naphthalenesulfonate With sodium carbonate at 0 - 50℃;
3,3'-dichlorobenzidine
91-94-1

3,3'-dichlorobenzidine

sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

C32H20Cl2N6O6S2(2-)*2Na(1+)

C32H20Cl2N6O6S2(2-)*2Na(1+)

Conditions
ConditionsYield
Stage #1: 3,3'-dichlorobenzidine With hydrogenchloride; sodium nitrite at 0℃;
Stage #2: sodium 4-amino-1-naphthalenesulfonate With sodium carbonate at 0 - 50℃;
66 mg
3,3'-diaminodiphenyl sulfone
599-61-1

3,3'-diaminodiphenyl sulfone

sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

bis-(3-(1-amino-4-sulfo-2-naphthylazo)phenyl)sulfone disodium salt

bis-(3-(1-amino-4-sulfo-2-naphthylazo)phenyl)sulfone disodium salt

Conditions
ConditionsYield
Stage #1: 3,3'-diaminodiphenyl sulfone With hydrogenchloride; sodium nitrite at 0℃;
Stage #2: sodium 4-amino-1-naphthalenesulfonate With sodium carbonate at 0 - 20℃;
sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

aniline
62-53-3

aniline

4-amino-3-(2-phenyl-1-diazenyl)-1-naphthalenesulfonic acid sodium salt

4-amino-3-(2-phenyl-1-diazenyl)-1-naphthalenesulfonic acid sodium salt

Conditions
ConditionsYield
Stage #1: aniline With hydrogenchloride; sodium nitrite at 0 - 5℃;
Stage #2: sodium 4-amino-1-naphthalenesulfonate With sodium carbonate at 0 - 20℃;
71 mg
sodium 4-amino-1-naphthalenesulfonate
130-13-2

sodium 4-amino-1-naphthalenesulfonate

dapsone
80-08-0

dapsone

bis-(4-(1-amino-4-sulfo-2-naphthylazo)phenyl)sulfone disodium salt

bis-(4-(1-amino-4-sulfo-2-naphthylazo)phenyl)sulfone disodium salt

Conditions
ConditionsYield
Stage #1: dapsone With hydrogenchloride; sodium nitrite at 0℃;
Stage #2: sodium 4-amino-1-naphthalenesulfonate With sodium carbonate at 0 - 20℃;
24 mg

130-13-2Relevant articles and documents

Surface grafted hyper-branched polyglycerol stabilized Ag and AuNPs heterogeneous catalysts for efficient reduction of Congo Red

Murugan, Eagambaram,Shanmugam, Paramasivam

, p. 426 - 438 (2016)

Six types of insoluble polymer-supported beads immobilized with Ag and AuNPs nanoparticle catalysts were synthesized using newly prepared three different types of polymer-supported poly(styrene)-co-poly(vinyl benzene chloride) matrix (PS-PVBC), surface grafted with (i) triethanolamine (TEA), (ii) glycidyl trimethyl ammonium chloride (GTMAC) and (iii) hyper-branched polyglycerol (HPG) and Ag and AuNPs as a catalytic moiety and thus yield polymer-supported nanoparticle catalysts viz., PS-PVBC-TEA-AgNPs and AuNPs, PS-PVBC-g-GTMAC-AgNPs and AuNPs and PS-PVBC-g-GTMAC-AgNPs and AuNPs catalyst respectively. These bead-shaped heterogonous nanoparticle catalysts were characterized by UV-Vis, FTIR, FESEM, HRTEM and TGA techniques. The efficiency for stabilization/loading of metal nanoparticles with respect to varied intensities of hyper-branched chain grafted onto their matrix was screened by determining their comparative catalytic activity. The catalytic potential of thse catalysts was inspected through reduction of Congo Red (CR) keeping pseudo first order identical reaction condition. The observed kobs values reveal that irrespective of metal the catalyst derived from hyper-branched polyglycerol as stabilizing agent viz., PS-PVBC-g-HPG-AgNPs and PS-PVBC-g-HPG-AuNPs shows (kobs = 3.98× 10-2 min-1 and kobs = 4.54 × 10-2 min-1) four and two times greater activity than the catalyst derived from TEA and GTMAC hyper-branched chain. Further, for the same reaction PS-PVBC-g-HPG-AuNPs showed more efficiency than the PS-PVBC-g-HPG AgNPs catalyst. The stability and reusability of the superior catalyst viz., PS-PVBC-g-HPG-AuNPs catalyst was observed to be good even at the sixth cycle. This catalyst can be continuously used to conduct the reduction of various dyes in continuous mode operation in industrial scale.

Cu/CuxS-Embedded N,S-Doped Porous Carbon Derived in Situ from a MOF Designed for Efficient Catalysis

Wang, Dongsheng,Fan, Mingyue,He, Tingyu,Zeng, Fanming,Hu, Xiaoli,Li, Chun,Su, Zhongmin

, p. 11468 - 11476 (2021)

The reasonable design of the precursor of a carbon-based nanocatalyst is an important pathway to improve catalytic performance. In this study, a simple solvothermal method was used to synthesize [Cu(TPT)(2,5-tdc)] ? 2H2O (Cu-MOF), which contains N and S atoms, in one step. Further in-situ carbonization of the Cu-MOF as the precursor was used to synthesize Cu/CuxS-embedded N,S-doped porous carbon (Cu/CuxS/NSC) composites. The catalytic activities of the prepared Cu/CuxS/NSC were investigated through catalytic reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP). The results show that the designed Cu/CuxS/NSC has exceptional catalytic activity and recycling stability, with a reaction rate constant of 0.0256 s?1, and the conversion rate still exceeds 90 % after 15 cycles. Meanwhile, the efficient catalytic reduction of dyes (CR, MO, MB and RhB) confirmed its versatility. Finally, the active sites of the Cu/CuxS/NSC catalysts were analyzed, and a possible multicomponent synergistic catalytic mechanism was proposed.

Graphene oxide nanocomposite magnetic microbeads for the remediation of positively charged aromatic compounds

Clamer, M.,Dalla Serra, M.,Micheli, V.,Minati, L.,Speranza, G.

, p. 3333 - 3340 (2020)

Integrating graphene as an inorganic nanostructure within a hydrogel matrix enables the creation of a unique hybrid composite combining the peculiar chemical and physical properties of graphene with the high porosity and stability of hydrogels as for example agarose gel. As a consequence, the resulting material forms a double-network system providing advantages deriving from both the components. In this study, we present the synthesis of novel magnetic porous agarose-based graphene oxide microbeads for the adsorption and separation of positively charged aromatic molecules. The hydrogel-based graphene oxide beads revealed an ultrafast adsorption kinetics for positively charged aromatic dyes. We tested this material for the purification of fluorescent-tagged biomolecules. In addition, reduced graphene oxide microbeads were decorated with palladium nanoparticles, showing a high catalytic activity towards the reduction of dyes by sodium borohydride. Our results show that magnetic agarose based graphene microbeads with enhanced physical-chemical properties can be used for several biochemical applications.

A rationally designed fluorescence chemosensor for on-site monitoring of carbon monoxide in air

Yan, Tengfei,Chen, Jin,Wu, Song,Mao, Zhiqiang,Liu, Zhihong

, p. 3296 - 3299 (2014)

A fluorescence chemsensor for carbon monoxide (CO), based on transformation of weakly fluorescent iodide to strong fluorescent amino product upon reacting with CO, shows abilities of quantitative measurement of CO in air at a level of 50-1000 ppm and real-time and on-site monitoring for CO flammation/explosion.

Energy and environmental applications of ultrasonically sulfur doped copper-nickel hydroxides with heterostructures

Karthik, Namachivayam,Edison, Thomas Nesakumar Jebakumar Immanuel,Atchudan, Raji,Sethuraman, Mathur Gopalakrishnan

supporting information, p. 126 - 136 (2017/09/22)

A series of sulfur doped copper-nickel hydroxides with heterojunctions were successfully fabricated on nickel foam by adjusting thiourea volume via a facile sonochemical pathway. The effect of volume of thiourea on the final morphology and chemical composition of the hybrids were also investigated by field-emission scanning electron microscopy, and X-ray photoelectron spectroscopy analyses. Furthermore, the electrochemical performance and catalytic activity of the as-obtained hybrids were also investigated. Among the tested electrode, the hybrid material fabricated using 6 ml of thiourea (TU-6) showed outstanding electrochemical properties comprising a high specific capacitance of about 2708 F g?1 at 5 A g?1. In addition, the TU-6 hybrid (catalyst) material displayed remarkable reductive degradation ability towards azo dyes viz., methyl orange (within 8 min) and congo red (within 20 min) in the presence of sodium borohydride (reducing agent) with fast kinetics and good reproducibility, respectively. The exceptional electrochemical performance and excellent catalytic activity of TU-6 hybrid electrode may be attributed to the formation of catalytically active sulfur doped copper-nickel hydroxides (CuS/Ni3S2/NiOOH) three-interface synergistic effect, and unique porous micro-rosette-like texture which increased the diffusion rate and adsorption capacity. The adopted strategy is a simple and generic way for material fabrication to solve the energy and environmental problems.

Method for synthesizing 1-naphthylamine-4-sodium sulfonate by gas-phase SO3 sulfonation method

-

Paragraph 0012; 0013; 0014; 0015; 0016; 0017, (2017/05/02)

The invention relates to a method for synthesizing 1-naphthylamine-4-sodium sulfonate by a gas-phase SO3 sulfonation method. The method is characterized in that gas SO3 and dry air are mixed and cooled, a mixture is introduced into a reaction vessel filled with 1-naphthylamine and an organic solvent for sulfonation, the reaction vessel is heated to the temperature of 160-190 DEG C for transposition, water and solid alkali are slowly added in the reaction vessel for neutralizing until the pH value is 7-9, and the material is subjected to standing and layering to obtain an oil phase and a water phase; the water phase is concentrated until the concentrate proportion is 1.20-1.22, the obtained concentrate is subjected to standing for 1-2 hours at the temperature of 60-80 DEG C, and then the material is separated to obtain the product 1-naphthylamine-4-sodium sulfonate. The method has the advantages of short reaction time, low energy consumption, high efficiency during the reaction process, and no three-waste generation.

Efficient degradation of azo dyes using Ag and Au nanoparticles stabilized on graphene oxide functionalized with PAMAM dendrimers

Rajesh, Rajendiran,Kumar, S. Senthil,Venkatesan, Rengarajan

supporting information, p. 1551 - 1558 (2014/05/06)

Herein, we report the stabilization of silver and gold nanoparticles (Ag/Au NPs) on graphene oxide (GO) functionalized with PAMAM dendrimers. The grafting of the PAMAM dendrimers on GO has been investigated using TGA and Raman spectral studies and the stabilization of the Ag/Au NPs on the dendritic structures has been confirmed using XRD, UV-Vis and FT-IR spectra, SEM and TEM studies. The catalytic activity of the prepared nanocatalysts towards the degradation of organic azo dyes, namely methyl orange and congo red, has been tested. The prepared nanocatalysts were found to exhibit excellent catalytic activity towards the complete degradation of both methyl orange and congo red within only a few seconds.

BICYCLIC DERIVATIVES AS MODULATORS OF VOLTAGE GATED ION CHANNELS

-

Page/Page column 50, (2008/06/13)

Bicyclic derivatives useful as ion channel antagonists are disclosed herein. The compositions thereof are useful for treating or relieving pain-related conditions.

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