| Identification | More | 【Name】
tert-Butylhydroquinone | 【CAS】
1948-33-0 | 【Synonyms】
1-T-BUTYL-1,4-DIHYDROXYBENZENE
2-(1,1-Dimethylethyl)-1,4-benzenediol
2-T-BUTYLHYDROQUINONE
2-TERT-BUTYL-1,4-BENZENEDIOL
2-TERT-BUTYL-1,4-DIHYDROXYBENZENE
2-tert-butylhydroquinone
Butylhydroquinone
MONO-TERT-BUTYLHYDROQUINONE
TBHQ
T-BUTYLHYDROQUINONE
TERT-BUTYLHYDROCHINONE
TERT-BUTYLHYDROQUINONE
TERTIARY BUTYL HYDROQUINONE
1-dimethylethyl)-4-benzenediol(1
2-(1,1-dimethylethyl)-4-benzenediol
2-t-Butyl-1,4-benzenediol
2-tert-butylhydroquinen
2-tetrabutyl-1,4-dihydroxybenzene
4-Benzenediol,2-(1,1-dimethylethyl)-1
banox20ba | 【EINECS(EC#)】
217-752-2 | 【Molecular Formula】
C10H14O2 | 【MDL Number】
MFCD00002344 | 【Molecular Weight】
166.22 | 【MOL File】
1948-33-0.mol |
| Safety Data | Back Directory | 【Hazard Codes 】
Xn | 【Risk Statements 】
R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin . | 【Safety Statements 】
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | 【RIDADR 】
UN3077 | 【WGK Germany 】
3
| 【RTECS 】
MX4375000
| 【HazardClass 】
9 | 【PackingGroup 】
III | 【HS Code 】
29072900 | 【Hazardous Substances Data】
1948-33-0(Hazardous Substances Data) |
| Hazard Information | Back Directory | 【General Description】
White to light tan crystalline powder or a fine beige powder. Very slight aromatic odor. | 【Reactivity Profile】
Phenols, such as TERT-BUTYLHYDROQUINONE(1948-33-0), 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. This chemical is incompatible with oxidizers. | 【Air & Water Reactions】
Insoluble in water. | 【Fire Hazard】
This chemical is combustible. |
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