|
PERI ACID | ||
PRODUCT IDENTIFICATION |
||
CAS NO. | 82-75-7 |
|
EINECS NO. |
201-437-1 |
|
FORMULA | C10H9NO3S | |
MOL WT. | 223.25 | |
H.S. CODE | ||
TOXICITY | ||
SYNONYMS | 8-Aminonaphthalene-1-sulphonic acid; | |
1-Naphthylamine-8-sulfonic Acid; 1-Amino-8-naphthalenesulfonic acid; | ||
SMILES |
|
|
CLASSIFICATION |
|
|
PHYSICAL AND CHEMICAL PROPERTIES |
||
PHYSICAL STATE | gray to reddish wet powder | |
MELTING POINT | ||
BOILING POINT | ||
SPECIFIC GRAVITY | ||
SOLUBILITY IN WATER | ||
AUTOIGNITION | ||
pH | ||
VAPOR DENSITY | ||
NFPA RATINGS | ||
REFRACTIVE INDEX |
||
FLASH POINT |
|
|
STABILITY | Stable under ordinary conditions. | |
GENERAL DESCRIPTION & APPLICATIONS |
||
Naphthylamine is an aromatic amine which can be obtained from nitronaphthalene
(with iron and hydrochloric acid) or naphthol with sodium acetate, ammonium
chloride. There are position isomers; 1-naphthylamine and 2-naphthylamine.
2-Naphthylamine
was used as an Intermediate for wide application target molecules including
dyestuffs, agrochemicals, and antioxidants. But its use is restricted or
prohibited due to cancer suspect. Naphthylamine is the naphthalene homologues of aniline. Naphthylamine is the
starting material in the dye manufacturing and rubber industry. Numerous sulfo- and nitro-group substituted
naphthylamine on the ring system offer important roles to each characteristic
colours directly and in preparing next target colorants. Phenyl group
substituted naphthylamines are naphthalene homologues of phenylenediamines used
as parent compounds in vulcanization accelerators and in antioxidants for rubber
industry. Naphthylamine can be oxidized by chromic acid into naphthoquinone
which is the fundamental ring structure related with vitamin K.
Tetrahydronaphthylamine can be oxidized by potassium permanganate into adipic
acid. Naphthyl structure is found as a ligand in transition-metal catalyts
particularly in the form of bi-naphthyl which is composed of two naphthyl rings
connected at one carbon site on each ring.
Sulfonic acid is a compound with general formula RSO2OH, where R is an aliphatic or aromatic hydrocarbon. It is a derivative of sulfuric acid (HOSO2OH) where an OH has been replaced by a carbon group or a compound where a hydrogen atom has been replaced by treatment with sulfuric acid; for example, benzene is converted to benzenesulfonic acid (water-soluble). Sulfonic acid has a sulfur atom bonded to a carbon atom of a hydrocarbon and bonded also to three oxygen atoms, one of which has been attached to a hydrogen atom. Sulfonic acid is acidic due to the hydrogen atom, stronger than a carboxylic acid. Sulfonic acid is one of the most important organo sulfur compounds in organic synthesis. Sulfonic acids are used as catalysts in esterification, alkylation and condensation reactions. Sulfonates are salts or esters of sulfonic acid. Sulfonic salts are soluble in water. Sulfonic acid and its salts present in organic dyes provide useful function of water solubility and or improve the washfastness of dyes due to their capability of binding more tightly to the fabric. Peri Acid (1-naphthylamine-8-sulfonic Acid) is used directly in making several dyes and converted into numerous dye intermediates, as well as into tanning agents. |
||
SALES SPECIFICATION | ||
APPEARANCE |
gray to reddish wet powder | |
DIAZO CONTENT |
90% in (dry basis) |
|
TRANSPORTATION | ||
PACKING | 50kgs in drum | |
HAZARD CLASS | 6.1 (Packing Group: III) | |
UN NO. |
2811 |
|
OTHER INFORMATION | ||
Hazard Symbols: XI, Risk Phrases: 36/37/38, Safety Phrases: 26-36 |
||
PRICE |
||
|
|