Product
Supplier
Encyclopedia
Inquiry
Home > Encyclopedia > Phenyl J Acid

Phenyl J Acid

Phenyl J Acid structure

Phenyl J Acid 

structure
  • CAS No:

    119-40-4

  • Formula:

    C16H13NO4S

  • Chemical Name:

    Phenyl J Acid

  • Synonyms:

    2-Naphthalenesulfonic acid,4-hydroxy-7-(phenylamino)-;2-Naphthalenesulfonic acid,7-anilino-4-hydroxy-;1-Naphthol-3-sulfonic acid,6-anilino-;4-Hydroxy-7-(phenylamino)-2-naphthalenesulfonic acid;Phenyl I acid;Phenyl J Acid;2-Phenylamino-5-naphthol-7-sulfonic acid;5-Hydroxy-2-(phenylamino)-7-naphthalenesulfonic acid;2-Anilino-5-hydroxy-7-naphthalenesulfonic acid;N-Phenyl I acid;N-Phenyl J acid;7-Anilino-4-hydroxy-2-naphthalenesulfonic acid;2-Anilino-5-naphthol-7-sulfonic acid;NSC 10451;NSC 1745;NSC 37153;6-Phenylamino-1-hydroxynaphthalene-3-sulfonic acid;6-(Phenylamino)-1-naphthol-3-sulfonic acid;1-Hydroxy-6-anilinonaphthalene-3-sulfonic acid;121696-48-8

  • Categories:

    Pharmaceutical Intermediates  >  Bulk Drug Intermediates

Description

DryPowder

Phenyl J Acid Basic Attributes

315.34

315.34

204-320-3

758U5197SS

37153|10451|1745

DTXSID0044787

2922199090

Characteristics

95

0.57

DryPowder

1.5±0.1 g/cm3

1.735

Safety Information

22-24/25

P264, P280, P305+P351+P338, P33, P313

H319

|Warning|H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]|P264, P280, P305+P351+P338, and P337+P313|Aggregated GHS information provided by 78 companies from 6 notifications to the ECHA C&L Inventory.

Phenyl J Acid Use and Manufacturing

Methods of Manufacturing

It is derived from the condensation of J acid and aniline in sodium bisulfite medium. Put the J acid, aniline, sodium bisulfite, and sodium carbonate into the water, raise the temperature to 104-106°C in 1.5h, keep it for 40h, and the pressure is about 0.1MPa. After heat preservation, cool to 30°C and filter. The filter cake is added to the water, the temperature is raised to 80-85°C, and concentrated sulfuric acid is added in a trickle to decompose the excess sodium bisulfite to release sulfur dioxide, and the material liquid remains blue to the Congo red test paper. After most of the sulfur dioxide has escaped, stir for another 1h, cool to 30°C, filter, and wash the filter cake with saturated brine to obtain a paste with a content of ≥40%, namely N-phenyl J acid. Raw material consumption quota: J acid (amino value ≥90%) 900kg/t, aniline (99.5%) 360kg/t, sodium bisulfite (99%) 500kg/t, sulfuric acid (92.5%) 630kg/t, soda ash (98 %) 28kg/t.

Uses

This product is a dye intermediate, used to synthesize azo dye direct copper salt green BTL, copper salt blue FBGL and copper salt purple BBL.


Intermediates

Synthetic dye and pigment manufacturing|2-Naphthalenesulfonic acid, 4-hydroxy-7-(phenylamino)-: ACTIVE

Computed Properties

Molecular Weight:315.3
XLogP3:1.4
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:315.05652907
Monoisotopic Mass:315.05652907
Topological Polar Surface Area:95
Heavy Atom Count:22
Complexity:469
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Material

Recommended Suppliers of Phenyl J Acid

Scan the QR Code to Share

Feedback & Suggestions
Send Message

Thank you for your feedback. If you require further assistance, please contact us by email at info@echemi.com or call us at +86-532-55729510.