Name | 2-hydroxy-3-(3-methylbut-2-enyl)-1,4-naphthoquinone |
Synonyms | Lapachol CI 75490 LAPACHOL C.I. 75490 NATURAL YELLOW 16 C.I. Natural Yellow 16 2-hydroxy-3-(3-methyl-2-butenyl)-4-naphthoquinone 2-hydroxy-3-(3-methylbut-2-enyl)-1,4-naphthoquinone 2-HYDROXY-3-(3-METHYLBUT-2-ENYL)-1,4-NAPHTHOQUINONE 2-HYDROXY-3-(3-METHYL-2-BUTENYL)-1,4-NAPHTHOQUINONE 2-Hydroxy-3-(3-methyl-2-butenyl)-1,4-naphthalenedione 1,4-Naphthoquinone, 2-hydroxy-3-(3-methyl-2-butenyl)- 4-hydroxy-3-(3-methylbut-2-en-1-yl)naphthalene-1,2-dione 2-hydroxy-3-(3-methylbut-2-en-1-yl)naphthalene-1,4-dione |
CAS | 84-79-7 |
EINECS | 201-563-7 |
InChI | InChI=1/C15H14O3/c1-9(2)7-8-12-13(16)10-5-3-4-6-11(10)14(17)15(12)18/h3-7,18H,8H2,1-2H3 |
InChIKey | CIEYTVIYYGTCCI-UHFFFAOYSA-N |
Molecular Formula | C15H14O3 |
Molar Mass | 242.27 |
Density | 1.2077 (rough estimate) |
Melting Point | 141-143°C(lit.) |
Boling Point | 325.09°C (rough estimate) |
Flash Point | 203.912°C |
Solubility | ethanol: soluble10mg/mL, clear, light yellow to yellow |
Vapor Presure | 0mmHg at 25°C |
Appearance | Solid |
Color | Yellow to Dark Yellow |
Merck | 13,5382 |
pKa | 4.81±0.10(Predicted) |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | 1.5740 (estimate) |
MDL | MFCD00001679 |
Hazard Symbols | Xn - Harmful |
Risk Codes | R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. 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. S36 - Wear suitable protective clothing. |
WGK Germany | 3 |
RTECS | QL8750000 |
Toxicity | LD50 in male, female BALB/c mice (g/kg): 0.487; 0.792 orally (Morrison) |
Color index | 75490 |
biological activity | Lapachol is a naphthoquinone, which was first isolated from Tabebuia avellanedae (liviridae). Lapachol has anti-abscess, anti-ulcer, anti-fungal, anti-cancer, anti-toxic, anti-inflammatory, anti-malarial, antiseptic, anti-tumor, anti-viral, antibacterial, anti-fungal and insecticidal activity. |
production method | preparation of quinone from the oxidation of dihydric phenol, phenol and aromatic amines |