Detail of > 98-32-8
- CAS Number:
- 98-32-8
- Name:
3-Amino-4-hydroxybenzenesulphonamide
- Formula:
- C6H8N2O3S
- Molecular Structure:

- Synonyms:
- 2-Amino-hydroxybenzene-4-sulphonamide;2Amino Phenol 4Sulphonamide;Metanilamide, 4-hydroxy-;Benzenesulfonamide, 3-amino-4-hydroxy-;3-Amino-4-hydroxybenzenesulfonamide;Metanilamide, 4-hydroxy- (8CI);4-Hydroxymetanilamide;Aminophenol sulfamide;2-Amino Phenol-4-Sulphonamide;
- Molecular Weight:
- 188.20
- EINECS:
- 202-657-0
- Density:
- 1.58 g/cm3
- Melting Point:
- 199-201 °C
- Boiling Point:
- 454.5 °C at 760 mmHg
- Flash Point:
- 228.7 °C
- Hazard Symbols:
Xi- Risk Codes:
- 36/37/38
- Safety:
- 26-36Details
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Reference
- 1:2-Metal-complex azo dyes
- 1:2-Metal-complex azo dyes. Kubicki, Edward; Hencel, Maria; Szymanska, Krystyna; Salagacki, Ryszard (Osrodek Badawczo-Rozwojowy Przemyslu Barwinikow, Pol.). Pol. PL 82987 16 Aug 1976, 4 pp (Polish). (Poland).Some commonly used reagents like 61993-71-3 and 85-12-1 are used in this experiment. CODEN: POXXA7. CLASS: IC: C09B045-04. APPLICATION: PL 72-155502 20 May 1972. DOCUMENT TYPE: Patent CA Section: 40 (Dyes, Fluorescent Whitening Agents, and Photosensitizers) Title dyes (I; R, R, R1, R2, R3 = atoms or groups at any position of the benzene ring, e.g. H, halogen, Me, NO2, sulfonamide; Z = coupling component residue with O atom ortho to N:N group; M = Cr or Co; X+ = alkali metal cation or NH4+) were prepd. by reaction of II or III with Cr or Co salts. Thus, 2,4-H2N(H2NSO2)C6H3OH [98-32-8] was diazotized and coupled with 4,1-AcNHC10H6OH [85-12-1], the product treated with aq. NaOH and aq. CoCl2, heated 1 h at 85.degree., and salted to give the 1:2 metal complex dye [61993-71-3], which dyed wool, silk, and polyamide fibers deep red shades. .
- Metallized 1:2-type azo dyes containing chromium or cobalt
- Metallized 1:2-type azo dyes containing chromium or cobalt. Hahn, Witold; Osinski, Janusz (Pabianickie Zaklady Farmaceutyczne "Polfa", Pol.). Pol. PL 120060 B1 25 Oct 1983, 4 pp. (Polish). (Poland). CODEN: POXXA7. CLASS: IC: C09B045-02. APPLICATION: PL 79-215076 20 Apr 1979. DOCUMENT TYPE: Patent CA Section: 41 (Dyes, Organic Pigments, Fluorescent Brighteners, and Photographic Sensitizers) The title dyes are prepd. by treatment of monoazo dyes I (R = H, NO2, SO2NH2; R1 = H, Cl, NO2, SO2NH2; R2 = H, NO2; R3 = H, SO2NH2; R4 = Br, Cl, Me, OMe, NH2; and I contain £2 SO2NH2 or their derivs.) with compds. easily yielding Cr or Co. Thus, 18.8 g 2-amino-4-sulfamoylphenol [98-32-8] was diazotized and coupled with 27.8 g 7-bromo-2-methylpyrazolo[3,2-b]quinazolin-9(4H)-one [90375-25-0] in aq. EtOH contg. NH3 and NaOH. The obtained suspension of monoazo dye [90375-29-4] was heated to 95° and treated with 7.8 g Na2Cr2O7.In this experiment, several chemicals are used like 90385-01-6 and 34373-12-1 2H2O and 14 g glucose in 60 vol. parts H2O and heated at the boiling temp. for 3 h to give 60 g dye [90384-94-4] dyeing wool, polyamide fibers and leather from neutral or weakly acidic baths in bordeaux-blue shades. .
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