Identification | More | 【Name】
2-Hydroxy-1,4-naphoquinone | 【CAS】
83-72-7 | 【Synonyms】
2-Hydroxy-1,4-naphoquinone 2-HYDROXY-1,4-NAPHTHAQUINONE 2-HYDROXY-1,4-NAPHTHOQUINONE 2-HYDROXY-P-NAPHTHOQUINONE CI 75480 JAROCOL LAWSONE LAWSONE NATURAL ORANGE 6 1,4-Naphthalenedione,2-hydroxy- 1,4-Naphthoquinone, 2-hydroxy- 2-Hydroxy-1,4-naphthalenedione 2-hydroxy-4-naphthalenedione 2-hydroxy-4-naphthoquinone 2-Hydroxynaphthoquinone 4-Naphthalenedione,2-hydroxy-1 C.I. Natural Orange 6 c.i.naturalorange6 Flower Of Paradise flowerofparadise Hana | 【EINECS(EC#)】
201-496-3 | 【Molecular Formula】
C10H6O3 | 【MDL Number】
MFCD00001678 | 【Molecular Weight】
174.15 | 【MOL File】
83-72-7.mol |
Safety Data | Back Directory | 【Hazard Codes 】
Xi,Xn | 【Risk Statements 】
R36/37/38:Irritating to eyes, respiratory system and skin . R68:Possible risk of irreversible effects. R36:Irritating to the eyes. R22:Harmful if swallowed. | 【Safety Statements 】
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 . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . S36:Wear suitable protective clothing . | 【WGK Germany 】
3
| 【RTECS 】
QL8200000
|
Hazard Information | Back Directory | 【General Description】
Yellow prisms or yellow powder. | 【Reactivity Profile】
Phenols, such as 2-HYDROXY-1,4-NAPHTHOQUINONE(83-72-7), do not behave as organic alcohols, as one might guess from the presence of a hydroxyl (-OH) group in their structure. Instead, they react as weak organic acids. Phenols and cresols are much weaker as acids than common carboxylic acids (phenol has Ka = 1.3 x 10^[-10]). These materials are incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may ignite the gas. Heat is also generated by the acid-base reaction between phenols and bases. Such heating may initiate polymerization of the organic compound. Phenols are sulfonated very readily (for example, by concentrated sulfuric acid at room temperature). The reactions generate heat. Phenols are also nitrated very rapidly, even by dilute nitric acid. Nitrated phenols often explode when heated. Many of them form metal salts that tend toward detonation by rather mild shock. | 【Air & Water Reactions】
Insoluble in water. | 【Health Hazard】
ACUTE/CHRONIC HAZARDS: This compound may be absorbed through the skin and can cause skin irritation. | 【Fire Hazard】
Flash point data for this chemical are not available but 2-HYDROXY-1,4-NAPHTHOQUINONE is probably combustible. |
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