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Peri acid

Peri acid Structure
CAS No.
82-75-7
Chemical Name:
Peri acid
Synonyms
8-AMINONAPHTHALENE-1-SULFONIC ACID;PERI ACID;1,8-AMINO ACID;Perigastric acid;Schollkopf's acid (VAN);8-SULFO-1-NAPHTHYLAMINE;1.8 Clevs Acid(Peri Acid);1-AMINO-8-SULFONAPHTHALENE;8-Naphthol-1-sulfonic acid;Peri acid ISO 9001:2015 REACH
CBNumber:
CB0680336
Molecular Formula:
C10H9NO3S
Molecular Weight:
223.25
MOL File:
82-75-7.mol
Modify Date:
2024/6/4 15:29:52

Peri acid Properties

Melting point >350°C
Boiling point 220°C (rough estimate)
Density 1.3588 (rough estimate)
refractive index 1.6500 (estimate)
pka pK1: 5.03 (25°C)
form powder to crystal
color Light yellow to Brown
Water Solubility 0.2g/L(21 ºC)
Merck 14,6405
BRN 983230
CAS DataBase Reference 82-75-7(CAS DataBase Reference)
EPA Substance Registry System 1-Naphthalenesulfonic acid, 8-amino- (82-75-7)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H335-H315-H319
Precautionary statements  P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Hazard Codes  C
Risk Statements  34
Safety Statements  26-27-36-45
TSCA  Yes
HS Code  29214500
NFPA 704
0
1 0

Peri acid price More Price(5)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemicals (India) A0350 8-Amino-1-naphthalenesulfonic Acid 82-75-7 25G ₹2700 2022-05-26 Buy
ALFA India ALF-L17616-36 8-Aminonaphthalene-1-sulfonic acid, 98% 82-75-7 500g ₹26000 2022-05-26 Buy
TCI Chemicals (India) A0350 8-Amino-1-naphthalenesulfonic Acid 82-75-7 100G ₹5200 2022-05-26 Buy
ALFA India ALF-L17616-22 8-Aminonaphthalene-1-sulfonic acid, 98% 82-75-7 100g ₹7314 2022-05-26 Buy
ALFA India ALF-L17616-14 8-Aminonaphthalene-1-sulfonic acid, 98% 82-75-7 25g ₹2700 2022-05-26 Buy
Product number Packaging Price Buy
A0350 25G ₹2700 Buy
ALF-L17616-36 500g ₹26000 Buy
A0350 100G ₹5200 Buy
ALF-L17616-22 100g ₹7314 Buy
ALF-L17616-14 25g ₹2700 Buy

Peri acid Chemical Properties,Uses,Production

Chemical Properties

Dark green powder. 1-Aminonaphthalene-8-sulfonic acid [82- 75-7]. (8-aminonaphthalene-1-sulfonic acid), Peri acid, C10H9NO3S, Mr 223.24, crystallizes as the monohydrate and is sparingly soluble even in boiling water. The sodium salt is also sparingly soluble in water. Caustic fusion at 200℃ produces 8-amino-1- naphthol, whereas slow hydrolysis with 10 % sodium hydroxide at 220 – 260℃ yields 1,8- dihydroxynaphthalene. Sulfonation with cold 10 % oleum produces 1-aminonaphthalene-4,8- disulfonic acid, whereas hot concentrated sulfuric acid results in slow isomerization into naphthionic acid.

Uses

Intermediate of dyestuff. Dehydration with phosphorus oxychloride yields naphthosultam, and diazotization followed by hydrolysis results in naphthosultone, the intermediate for 1- hydroxynaphthalene-8-sulfonic acid. Diazotization followed by a Sandmeyer cyanide reaction gives 8-cyanonaphthalene-1-sulfonic acid, one of the most industrially important Sandmeyer reaction products because the nitrile forms the lactam, naphthostyril [130-00-7], upon treatment with concentrated alkali at 185℃. Hydrolysis of naphthostyril with dilute alkali yields 8-aminonaphthalene-1-carboxylic acid, which is the key intermediate for production of anthanthrone vat dyes via 1,10 -binaphthyl8,80 -dicarboxylic acid.

Production Methods

Naphthalene is converted to naphthalene-1-sulfonic acid. The crude sulfonation product is diluted with sulfuric acid, and 67.5 % nitric acid is added slowly at 30℃ to give the 5- and 8-nitro derivatives. The products are converted to the readily soluble magnesium salts by addition of a slurry of dolomite. The reaction mixture is neutralized with chalk and filtered hot. The filtrate is run into a suspension of iron powder in boiling water, which is kept slightly acidic with sulfuric acid. When reduction is complete, dissolved iron is precipitated by addition of magnesia, the iron residues are filtered off while hot, and the resulting liquor is acidified to pH 4.5 with sulfuric acid to give 99 % pure Peri acid in 48 % yield. The filtrates are further acidified to precipitate crude Laurent’s acid. This may be purified via its magnesium salt to give a 17 % yield of pure 1,5-isomer.

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8-azanylnaphthalene-1-sulfonic acid 1,8-Naphthylaminesulfonic acid 1-Aminonaphthalene-8-sulfonic acid NAPHTHYLAMINOMONOSULFONIC ACID PERI ACID 1-Amino-8-naphthalenesulfonic Acid 1-Naphthylamine-8-sulfonic Acid Peri Acid 1.8 Clevs Acid(Peri Acid) 1-Amino-8-naphthalene sulfonate 1-Aminonaphthalene-8-sulfonate Naphthylaminemonosulfonic acid S Schollkopf's acid (VAN) 8-amino-1-naphthalenesulfonicaci 8-Naphthylamine-1-sulfonicacid 1,8-AMINO ACID 1-AMINO-8-NAPHTHALENESULFONIC ACID 1-AMINO-8-SULFONAPHTHALENE 8-AMino-1-naphthalenesulfonic acid, 98%, 98% 1-NAPHTHYLAMINE-8-SULFONIC ACID 8-AMINO-1-NAPHTHALENESULFONIC ACID 8-AMINONAPHTHALENE-1-SULPHONIC ACID 8-SULFO-1-NAPHTHYLAMINE ALPHA-NAPHTHYLAMINE-8-SULFONIC ACID 1-Amino-8-naphtalenesulfonic acid 1-Naphthylamine-8-sulphonic acid 8-amino-1-naphthalenesulfonic acid (peri acid) 1-Naphthalenesulfonic acid, 8-amino- 8-Naphthol-1-sulfonic acid 8-Amino-1-naphthalenesulfonicAcid> Peri acid ISO 9001:2015 REACH 8-AMINONAPHTHALENE-1-SULFONIC ACID Peri acid/8-Amino-1-naphthalenesulfonic acid Perigastric acid 82-75-7 Intermediates of Dyes and Pigments bc0001