Molecular Formula | C11H8O3 |
Molar Mass | 188.18 |
Density | 1.43 g/cm3 (23℃) |
Melting Point | 218-221°C(lit.) |
Boling Point | 283.17°C (rough estimate) |
Flash Point | >150°C |
Water Solubility | PRACTICALLY INSOLUBLE |
Solubility | 0.072g/l practically insoluble |
Vapor Presure | 4.68E-06mmHg at 25°C |
Appearance | Yellow crystal |
Color | Yellow to beige-brown |
Maximum wavelength(λmax) | ['395nm(H2O (pH 3.5))(lit.)'] |
Merck | 14,4835 |
BRN | 744100 |
pKa | 3.02±0.30(Predicted) |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | 1.7160 (estimate) |
MDL | MFCD00004103 |
Physical and Chemical Properties | Yellow rhombic lamellar crystals. |
Use | It is mainly used for the manufacture of phenol as and other intermediates of various phenols, and can also be used as intermediates for pharmaceuticals and organic pigments |
Risk Codes | R22 - Harmful if swallowed R36 - Irritating to the eyes R36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S37/39 - Wear suitable gloves and eye/face protection |
WGK Germany | 1 |
RTECS | QL1755000 |
TSCA | Yes |
HS Code | 29182910 |
Toxicity | The acute oral LD50 of 3-Hydroxy-2-naphthoic acid in rats was 823-1040 mg/kg bw. |
NIST chemical information | information provided by: webbook.nist.gov (external link) |
EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
Application | is mainly used for the manufacture of phenol as and other intermediates of various phenols, also can be used as pharmaceutical and organic pigment intermediates is mainly used for the manufacture of phenol as and other various phenol intermediates, but also the production of pharmaceutical and organic pigment intermediates. This product is mainly used for the manufacture of phenol as and other various phenol intermediates, can also be used in medicine, high-grade organic pigment intermediates. |
production method | 2-naphthol reacts with caustic soda to form 2-naphthol sodium salt, which is dewatered by distillation under reduced pressure, anhydrous 2-naphthol sodium salt is obtained, and carboxylation reaction is carried out with carbon dioxide to generate 2-naphthol and 2,3-acid disodium salt, the resin is decomposed to remove 2-naphthol, and then neutralized with sulfuric acid, acidification yields 3-hydroxy-2-naphthoic acid. After Suction filtration, centrifugal separation and drying, the finished product is obtained. Raw material consumption quota: 2-naphthol 1047kg/t, liquid alkali (30%)1950kg/t, sulfuric acid (92.5%)845kg/t, sodium bicarbonate 25kg/t, carbon dioxide 692kg/t. |
toxic substance data | information provided by: pubchem.ncbi.nlm.nih.gov (external link) |