Product Name

  • Name

    Naphthalene-2-sulfonic acid

  • EINECS 204-375-3
  • CAS No. 120-18-3
  • Article Data83
  • CAS DataBase
  • Density 1.423 g/cm3
  • Solubility Soluble in water, ethanol and ethyl ether
  • Melting Point 124 °C
  • Formula C10H8O3S
  • Boiling Point 525.7°C at 760 mmHg
  • Molecular Weight 208.238
  • Flash Point 271.7°C
  • Transport Information UN 2583 8/PG 2
  • Appearance off white powder
  • Safety 26-36/37/39-45-16
  • Risk Codes 35-11
  • Molecular Structure Molecular Structure of 120-18-3 (Naphthalene-2-sulfonic acid)
  • Hazard Symbols CorrosiveC,FlammableF
  • Synonyms 2-Naphthylsulfonicacid;2-Sulfonaphthalene;Dirinal NSK;b-Naphthalenesulfonic acid;b-Naphthylsulfonic acid;Kyselina 2-naftalensulfonova;2-Naphthalenesulfonic acid;
  • PSA 62.75000
  • LogP 3.16730

Synthetic route

naphthalene-2-sulfinic acid
613-49-0

naphthalene-2-sulfinic acid

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

Conditions
ConditionsYield
Stage #1: naphthalene-2-sulfinic acid With oxygen In N,N-dimethyl-formamide at 60℃; for 16h;
Stage #2: Acidic conditions;
97%
With N,N,N,N,N,N-hexamethylphosphoric triamide; oxygen; potassium hydroxide In N,N-dimethyl-formamide at 60℃; under 760.051 Torr; for 28h; Reagent/catalyst; Temperature; Solvent; Pressure; Sealed tube;93%
2-Naphthalenesulfonyl chloride
93-11-8

2-Naphthalenesulfonyl chloride

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

Conditions
ConditionsYield
Stage #1: 2-Naphthalenesulfonyl chloride With dmap; N-ethyl-N,N-diisopropylamine In dichloromethane at 22℃;
Stage #2: With trifluoroacetic acid In dichloromethane Further stages.;
94%
With water In acetone at 30℃; Kinetics; Mechanism; Thermodynamic data; other temperatures; ΔH(excit.), ΔS(excit.); various concentrations of the reagent and substrate;
Multi-step reaction with 2 steps
1: alcohol; zinc
2: water
View Scheme
2-Naphthalenethiol
91-60-1

2-Naphthalenethiol

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

Conditions
ConditionsYield
With dihydrogen peroxide; methyltrioxorhenium(VII) In acetonitrile at 20℃;94%
With dihydrogen peroxide; trichlorophosphate In water at 80℃; for 1.5h; Micellar solution;94%
bis(2-naphthyl)disulfide
5586-15-2

bis(2-naphthyl)disulfide

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

Conditions
ConditionsYield
With dihydrogen peroxide; trichlorophosphate In water at 80℃; for 1.16667h; Micellar solution;94%
Stage #1: bis(2-naphthyl)disulfide With oxygen; potassium hydroxide In N,N-dimethyl-formamide at 60℃; for 16h;
Stage #2: Acidic conditions;
64%
naphthalene
91-20-3

naphthalene

A

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

B

1-naphthalenesulfonic acid
85-47-2

1-naphthalenesulfonic acid

Conditions
ConditionsYield
With sulfuric acid at 160 - 170℃; for 1.5h;A 88.3%
B 8.51%
With sulfuric acid at 120℃; Product distribution; Rate constant; Thermodynamic data; activation energy; microwave or irradiation; regioselectivity;
With sulfuric acid at 120℃; for 0.5h; Product distribution; microwave activation; various power, temperature, reaction time, H2SO4 concentration;
naphthalene
91-20-3

naphthalene

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

Conditions
ConditionsYield
With 1,3-disulfonic acid imidazolonium chloride In water at 50℃; for 0.216667h; Green chemistry; regioselective reaction;72%
With sulfur trioxide In nitrobenzene at 20℃; for 4h;62%
With sulfuric acid at 90℃; for 2h;55%
1-Cyclopropyl--β-naphthylsulfonat
7515-55-1

1-Cyclopropyl--β-naphthylsulfonat

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

Conditions
ConditionsYield
With ethanol at 30 - 40℃; Kinetics; other reaction partners;
n-Heptyl-β-naphthylsulfonat
7515-59-5

n-Heptyl-β-naphthylsulfonat

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

Conditions
ConditionsYield
With ethanol at 30 - 40℃; Kinetics; other reaction partners;
4-Cyclopropyl-butyl-β-naphthylsulfonat
7515-56-2

4-Cyclopropyl-butyl-β-naphthylsulfonat

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

Conditions
ConditionsYield
With ethanol at 40 - 50℃; Kinetics; other reaction partners;
cis--β-naphthylsulfonat
7572-48-7

cis--β-naphthylsulfonat

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

Conditions
ConditionsYield
With ethanol at 60℃; Rate constant;
trans--β-naphthylsulfonat
7515-74-4

trans--β-naphthylsulfonat

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

Conditions
ConditionsYield
With ethanol at 60℃; Rate constant; other reaction partners;
Naphthalin-2-sulfonsaeure-pentylester
7515-54-0

Naphthalin-2-sulfonsaeure-pentylester

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

Conditions
ConditionsYield
With ethanol at 60℃; Rate constant; other reaction partners;
Naphthalin-2-sulfonsaeure-<4-phenyl-but-3-en-1-ylester>
7515-57-3

Naphthalin-2-sulfonsaeure-<4-phenyl-but-3-en-1-ylester>

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

Conditions
ConditionsYield
With ethanol at 60℃; Rate constant; other reaction partners;
Naphthalin-2-sulfonsaeure-<4-phenyl-butylester>
7572-50-1

Naphthalin-2-sulfonsaeure-<4-phenyl-butylester>

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

Conditions
ConditionsYield
With ethanol at 60℃; Rate constant; other reaction partners;
1-<4-Fluor-phenyl>--β-naphthylsulfonat
7515-58-4

1-<4-Fluor-phenyl>--β-naphthylsulfonat

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

Conditions
ConditionsYield
With ethanol at 60℃; Rate constant; other reaction partners;
1-<4-Brom-phenyl>--β-naphthylsulfonat
7572-49-8

1-<4-Brom-phenyl>--β-naphthylsulfonat

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

Conditions
ConditionsYield
With ethanol at 60℃; Rate constant;
methyl naphthalene-2-sulfonate
5138-53-4

methyl naphthalene-2-sulfonate

A

methylene chloride
74-87-3

methylene chloride

B

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

Conditions
ConditionsYield
With chloride; triethylhexadecylammonium chloride In water at 25℃; Rate constant; Equilibrium constant;
With chloride; cetyltripropylammonium chloride In water at 25℃; Rate constant; Equilibrium constant;
With chloride; hexadecyltributylammonium chloride In water at 25℃; Rate constant; Equilibrium constant;
naphthalene
91-20-3

naphthalene

A

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

B

1-naphthalenesulfonic acid
85-47-2

1-naphthalenesulfonic acid

C

naphthalene-1,7-disulphonic acid
5724-16-3

naphthalene-1,7-disulphonic acid

D

naphthalene-1,6-disulfonic acid
525-37-1

naphthalene-1,6-disulfonic acid

E

naphthalene-1,5-disulfonate
81-04-9

naphthalene-1,5-disulfonate

Conditions
ConditionsYield
With sulfur trioxide; water Product distribution; multistep reaction; various reaction conditions;
naphthalene
91-20-3

naphthalene

A

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

B

1-naphthalenesulfonic acid
85-47-2

1-naphthalenesulfonic acid

C

naphthalene-1,6-disulfonic acid
525-37-1

naphthalene-1,6-disulfonic acid

D

naphthalene-1,5-disulfonate
81-04-9

naphthalene-1,5-disulfonate

Conditions
ConditionsYield
With sulfur trioxide; water 1.) CH2Cl2, 22 deg C, 60 min, 2.) 70 - 80 deg C, 30 min; Multistep reaction. Further byproducts given. Title compound not separated from byproducts;
Naphthalene-2-sulfonic acid 4-tert-butoxycarbonylamino-2,2-dimethyl-butyl ester
1027174-15-7

Naphthalene-2-sulfonic acid 4-tert-butoxycarbonylamino-2,2-dimethyl-butyl ester

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

Conditions
ConditionsYield
With tetramethlyammonium chloride In N,N-dimethyl-formamide at 160℃; for 16h; Yield given;
Naphthalene-2-sulfonic acid 4-amino-2,2-dimethyl-butyl ester; compound with trifluoro-acetic acid

Naphthalene-2-sulfonic acid 4-amino-2,2-dimethyl-butyl ester; compound with trifluoro-acetic acid

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

Conditions
ConditionsYield
With pH: 7-8 In water Yield given;
naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

doxorubicin hydrochloride
25316-40-9

doxorubicin hydrochloride

doxorubicin naphthalene-2-sulfonate
1246449-86-4

doxorubicin naphthalene-2-sulfonate

Conditions
ConditionsYield
Stage #1: doxorubicin hydrochloride With potassium tert-butylate In tetrahydrofuran at 20.2 - 21.4℃; for 1.41667h; Inert atmosphere;
Stage #2: naphthalene-2-sulfonate In tetrahydrofuran at 20℃; for 1h; Inert atmosphere;
100%
naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

1,3,5-triphenylpent-2-en-1,5-dione
23800-57-9

1,3,5-triphenylpent-2-en-1,5-dione

2,4,6-triphenylpyrylium naphthalene-2-sulphonate

2,4,6-triphenylpyrylium naphthalene-2-sulphonate

Conditions
ConditionsYield
In isopropyl alcohol for 2h; Heating;99%
naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

β-naphthalene sulfonyl fluoride
325-12-2

β-naphthalene sulfonyl fluoride

Conditions
ConditionsYield
With 1,1,2,2-tetrafluoro-N,N-dimethylethan-1-amine In chloroform at 25℃; for 6h;99%
Stage #1: naphthalene-2-sulfonate With 1,3,5-trichloro-2,4,6-triazine; tetramethlyammonium chloride In acetonitrile at 60℃; for 12h;
Stage #2: With potassium hydrogen difluoride In acetone; acetonitrile at 20℃; for 12h;
74%
n-pentyl methyl ketone
110-43-0

n-pentyl methyl ketone

naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

4-amino-o-xylene
95-64-7

4-amino-o-xylene

N-2-heptyl-3,4-xylidine
78455-20-6

N-2-heptyl-3,4-xylidine

Conditions
ConditionsYield
With hydrogen; platinum99%
naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

4-ethyl-3-methylaniline
69450-94-8

4-ethyl-3-methylaniline

pentan-3-one
96-22-0

pentan-3-one

4-Ethyl-N-(1-ethylpropyl)-m-toluidine
69450-95-9

4-Ethyl-N-(1-ethylpropyl)-m-toluidine

Conditions
ConditionsYield
Pt/C98%
naphthalene-2-sulfonate
120-18-3

naphthalene-2-sulfonate

azelnidipine
123524-52-7

azelnidipine

Azelnidipine napsylate

Azelnidipine napsylate

Conditions
ConditionsYield
In ethyl acetate at 2 - 25℃; for 97h;97%

Naphthalene-2-sulfonic acid Consensus Reports

Reported in EPA TSCA Inventory.

Naphthalene-2-sulfonic acid Specification

The Naphthalene-2-sulfonic acid, with the CAS registry number 120-18-3, is also known as Kyselina 2-naftalensulfonova. It belongs to the product categories of Intermediates of Dyes and Pigments; Organic Building Blocks; Sulfonic/Sulfinic Acids; Sulfur Compounds. Its EINECS number is 204-375-3. This chemical's molecular formula is C10H8O3S and molecular weight is 208.23. What's more, its systematic name is 2-Naphthalenesulfonic acid. This chemical should be sealed and stored in a cool and ventilated place. Moreover, it should be protected from heat, fire and oxides. It is used in the production of naphthol and intermediates.

Physical properties of Naphthalene-2-sulfonic acid are: (1)ACD/LogP: 0.63; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -2.86 ; (4)ACD/LogD (pH 7.4): -2.87; (5)ACD/BCF (pH 5.5): 1.00; (6)ACD/BCF (pH 7.4): 1.00; (7)ACD/KOC (pH 5.5): 1.00; (8)ACD/KOC (pH 7.4): 1.00; (9)#H bond acceptors: 3; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 1; (12)Polar Surface Area: 62.75 Å2; (13)Index of Refraction: 1.67; (14)Molar Refractivity: 54.66 cm3; (15)Molar Volume: 146.326 cm3; (16)Polarizability: 21.669×10-24cm3; (17)Surface Tension: 58.79 dyne/cm; (18)Density: 1.423 g/cm3.

Preparation of Naphthalene-2-sulfonic acid: this chemical can be prepared by sulfonating naphthalene at the temperature of 160-166 °C. This reaction will need naphthalene as raw material, 98% sulfuric acid as sulfonating agent.

Uses of Naphthalene-2-sulfonic acid: it can be used to produce naphthalene-2-sulfonyl fluoride at the temperature of 25 °C. It will need reagent 1,1,2,2-tetrafluoroethyl-N,N-dimethylamine and solvent CHCl3 with the reaction time of 6 hours. The yield is about 99%.

Naphthalene-2-sulfonic acid can be used to produce naphthalene-2-sulfonyl fluoride at the temperature of 25 °C

When you are using this chemical, please be cautious about it as the following:
This chemical is highly flammable, so you should keep it away from sources of ignition - No smoking. It can cause severe burns. In case of contact with eyes, you should rinse immediately with plenty of water and seek medical advice. When using it, you need to wear suitable protective clothing, gloves and eye/face protection. In case of accident or if you feel unwell, you must seek medical advice immediately (show the label where possible).

You can still convert the following datas into molecular structure:
(1)SMILES: O=S(=O)(O)c2ccc1c(cccc1)c2
(2)Std. InChI: InChI=1S/C10H8O3S/c11-14(12,13)10-6-5-8-3-1-2-4-9(8)7-10/h1-7H,(H,11,12,13)
(3)Std. InChIKey: KVBGVZZKJNLNJU-UHFFFAOYSA-N

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
rat LD50 oral 4440mg/kg (4440mg/kg)   Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 39(10), Pg. 101, 1974.

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