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2-Aminonaphthalene-1-sulfonic acid is an organic compound that serves as a manufacturing intermediate and chemical building block in various industrial applications. It is characterized by its grey white to light pink powder form and is known for its role in the synthesis of dyes and other chemical compounds.

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  • China Biggest factory Manufacturer Supply High Quality 2-Aminonaphthalene-1-sulfonic acid CAS 81-16-3

    Cas No: 81-16-3

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  • 81-16-3 Structure
  • Basic information

    1. Product Name: 2-Aminonaphthalene-1-sulfonic acid
    2. Synonyms: TOBIAS ACID;1-Naphthalenesulfonic acid, 2-amino-;1-Naphthalenesulfonicacid,2-amino-;2-amino-1-naphthalenesulfonic;2-amino-1-naphthalenesulfonicaci;Kyselina 2-naftylamin-1-sulfonova;Kyselina tobiasova;kyselina2-naftylamin-1-sulfonova
    3. CAS NO:81-16-3
    4. Molecular Formula: C10H9NO3S
    5. Molecular Weight: 223.25
    6. EINECS: 201-331-5
    7. Product Categories: Intermediates of Dyes and Pigments;Intermediates;Organics
    8. Mol File: 81-16-3.mol
  • Chemical Properties

    1. Melting Point: 180 °C
    2. Boiling Point: 220°C (rough estimate)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.3588 (rough estimate)
    6. Refractive Index: 1.5250 (estimate)
    7. Storage Temp.: -20°C Freezer, Under inert atmosphere
    8. Solubility: DMSO (Slightly), Methanol (Slightly, Heated), Water (Slightly, Heated)
    9. PKA: pK1: 2.35 (25°C)
    10. Water Solubility: 4.083g/L(20 oC)
    11. Merck: 14,6406
    12. BRN: 613084
    13. CAS DataBase Reference: 2-Aminonaphthalene-1-sulfonic acid(CAS DataBase Reference)
    14. NIST Chemistry Reference: 2-Aminonaphthalene-1-sulfonic acid(81-16-3)
    15. EPA Substance Registry System: 2-Aminonaphthalene-1-sulfonic acid(81-16-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 36/37/38-40
    3. Safety Statements: 26-36/37/39
    4. RIDADR: 2585
    5. WGK Germany: 1
    6. RTECS: QK1250000
    7. TSCA: Yes
    8. HazardClass: 8
    9. PackingGroup: III
    10. Hazardous Substances Data: 81-16-3(Hazardous Substances Data)

81-16-3 Usage

Uses

Used in Azo Dye Industry:
2-Aminonaphthalene-1-sulfonic acid is used as an azo dye intermediate for the production of various colored compounds. Its chemical structure allows it to react with other molecules to form azo dyes, which are widely used in coloring fabrics, plastics, and other materials.
Used in Optical Brighteners Industry:
2-Aminonaphthalene-1-sulfonic acid is also utilized as a key component in the creation of optical brighteners. Optical brighteners are additives that enhance the appearance of materials by reflecting light more effectively, making them appear brighter and more vivid.
Used in Pharmaceutical Industry:
2-Aminonaphthalene-1-sulfonic acid is used as a reagent in the synthesis of 2-(2-naphthylamino)benzoxazole, which is obtained by reacting it with 2-chlorobenzoxazole. This synthesized compound has potential applications in the pharmaceutical industry, possibly for the development of new drugs or drug intermediates.
Used in Cosmetic Industry:
As a manufacturing intermediate, 2-Aminonaphthalene-1-sulfonic acid contributes to the production of monosulfo monoazo color additive D&C Red No. 34 and its lakes. These color additives are used in cosmetics to provide vibrant shades and enhance the visual appeal of various products.

Purification Methods

Crystallise the acid under nitrogen from boiling water and dry it in a steam oven [Bryson Trans Faraday Soc 47 522, 527 1951]. [Beilstein 14 III 2240, 14 IV 2792.]

Check Digit Verification of cas no

The CAS Registry Mumber 81-16-3 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 81-16:
(4*8)+(3*1)+(2*1)+(1*6)=43
43 % 10 = 3
So 81-16-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO3S/c11-9-6-5-7-3-1-2-4-8(7)10(9)15(12,13)14/h1-6H,11H2,(H,12,13,14)/p-1

81-16-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Alfa Aesar

  • (A18644)  2-Aminonaphthalene-1-sulfonic acid, 98%   

  • 81-16-3

  • 500g

  • 527.0CNY

  • Detail
  • Alfa Aesar

  • (A18644)  2-Aminonaphthalene-1-sulfonic acid, 98%   

  • 81-16-3

  • 2500g

  • 2113.0CNY

  • Detail
  • Aldrich

  • (291137)  2-Amino-1-naphthalenesulfonicacid  98%

  • 81-16-3

  • 291137-250G

  • 888.03CNY

  • Detail
  • Aldrich

  • (291137)  2-Amino-1-naphthalenesulfonicacid  98%

  • 81-16-3

  • 291137-1KG

  • 2,750.67CNY

  • Detail

81-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Naphthylamine-1-Sulfonic Acid

1.2 Other means of identification

Product number -
Other names 1-Naphthalenesulfonic acid, 2-amino-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
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:81-16-3 SDS

81-16-3Relevant articles and documents

Fibre reactive azo dyestuffs

-

, (2008/06/13)

Fiber reactive azo dyestuffs of the formula STR1 in which R=H or C1 -C6 alkyl, which can be substituted with OH, Hal, SO3 H or OSO3 H; Z=heterocyclic five or six membered ring; n, m=0, 1 or 2, wherein n+m=0, 1 or 2; Y=OH, OR, NR2 R3, OMe; and R2, R3, =H, R and R2, R3 and N can form a heterocyclic 5 or 6-membered ring.

Azo pigment compositions and process for their preparation

-

, (2008/06/13)

This invention is that of an azo pigment composition containing about 1 to 10 percent by weight of a nonionic alkyl polyglycoside dispersing agent. The polyglycosides useful in the invention have the general formulae: wherein: M is an oxygen, sulfur, nitrogen phosphorous or silicon atom; n is an integer from 8 to 18, preferably 8 to 11 and X represents the number average degree of polymerization having a numerical value from about 1 to about 2. These azo pigment compositions are prepared by conducting the azo pigment coupling reaction in the presence of said alkyl polyglycoside. The resulting pigment exhibit superior application properties in water based ink systems.

Reactive dye having both monochlorotriazinyl and vinylsulfone type reactive groups

-

, (2008/06/13)

A novel reactive monoazo dye, capable of giving cellulose fiber materials a deep orange to scarlet color and superior in build-up and chlorine fastness properties, represented by a free acid of the formula, STR1 wherein R1 is hydrogen, methyl or ethyl; R2 is an alkyl having 1 to 4 carbons that is either unsubstituted or substituted with hydroxy, cyano, alkoxy, halogen, carboxy, alkoxycarbonyl or sulfonic acid; Z is hydrogen or sulfonic acid; A is phenylene and is either unsubstituted or substituted with 1 or 2 substituents selected from the group consisting of methyl, ethyl, methoxy, ethoxy, chlorine, bromine and sulfonic acid, or natphthylene that is either unsubstituted or substituted with sulfonic acid; X is --SO2 CH=CH2 or --SO2 CH2 CH2 Y in which Y is a group that is splittable by alkalis; and m is an integer of 1 to 3.

Fiber reactive monoazo compounds having two vinylsulfone type fiber reactive groups in the molecule

-

, (2008/06/13)

A monoazo compound of the following formula in a free acid form, STR1 wherein A1 and A2 are phenylene or naphthylene, Z1 and Z2 are --SO2 CH=CH2 or --SO2 CH2 CH2 Y in which Y is a splittable group, R1 and R2 are hydrogen or alkyl, and D is sulfophenyl or sulfonaphthyl, provided that --A1 --Z1 and --A2 --Z2 are different from each other when D is sulfophenyl and both R1 and R2 are hydrogen, which is useful for dyeing or printing fiber materials to give dyed products of high fastness properties with extremely high color depth.

Solid phase acylation of aminosulfonic acids

-

, (2008/06/13)

This invention is directed to the acylation of aminosulfonic acids in the solid phase. Two discrete, sequential chemical reactions occur, i.e. (1) the neutralization of the aminosulfonic acid, and (2) the subsequent amine acylation, to produce an improved neutralized acyl-aminosulfonic acid at a reduced cost. Aminosulfonic acids having the general formula HO3 S-A-NH2 are acylated to neutralized acyl-aminosulfonic acids having the general formula RCONH-A-SO3 M, where A is an unsubstituted or substituted aliphatic, aromatic or heteroaromatic group and M is a neutralizing agent moiety. The yield is virtually quantitative.

Fiber-reactive disazo brown dye having vinylsulfone-type reactive group

-

, (2008/06/13)

A compound, or a salt thereof, represented by the following formula, STR1 wherein A is a substituted or unsubstituted phenylene or naphthylene group, B is STR2 in which R3 is a hydrogen atom or a lower alkyl, lower alkoxy, acylamino or ureido group, and R4 is a hydrogen atom or a lower alkyl or lower alkoxy group, R1 and R3 are independently a hydrogen atom or a substituted or unsubstituted lower alkyl group, X is a substituted or unsubstituted amino, lower alkoxy, substituted phenoxy or sulfo group, Y is --SO2 CH=CH2 or --SO2 CH2 CH2 Z, in which Z is a group capable of being split by the action of an alkali, and m is 2 or 3, which is useful for dyeing hydroxyl group- or amide group-containing fiber materials to give dyed products of a brown color having excellent fastness properties with good build-up property.

Reactive yellow dye having both monochlorotriazinyl and vinylsulfone type reactive groups

-

, (2008/06/13)

The compounds represented, in the form of free acid, by the following general formula (I): STR1 (wherein A is STR2 (wherein R3 and R4 are each hydrogen or a methyl, ethyl, methoxy, ethoxy, acetylamino, propionylamino, benzoylamino or ureido group, and R5 and R6 are each hydrogen or a methyl or methoxy group), R1 and R2 are each hydrogen or a methyl, ethyl or sulfomethyl group, X1 and X2 are each hydrogen, chlorine or a methyl, methoxy, carboxyl or sulfonic acid group, m is a number of 0, 1 or 2, and n is a number of 1 or 2, provided that the sum of m and n is 1, 2 or 3). These compounds are capable of dyeing cellulose fibers in yellow with excellent color fastness to hypochlorite, light, perspiration and sunlight and high acid stability.

Process for azo pigments

-

, (2008/06/13)

A pigment modifier composition for azo pigments is prepared in situ by chlorination of 2-hydroxy-3-naphthoic acid with a hypochlorite such that up to 10% of the acid is converted into 1-chloro-2-hydroxy-3-naphthoic acid.

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