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Products Intro: |
Product Name:2,6-Di-tert-butylphenol CAS:128-39-2 Purity:99% Package:100KG |
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Product Name:2,6-Di-tert-butylphenol, 98% CAS:128-39-2 Package:250g Remarks:A17244 |
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Products Intro: |
Product Name:2,6-Di-tert-butylphenol CAS:128-39-2 Purity:98.0%(GC) Package:500G;25G |
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| 2,6-Di-tert-butylphenol Basic information |
Product Name: | 2,6-Di-tert-butylphenol | Synonyms: | 2,6-(1,1-Dimethylethyl)phenol;2,6-bis(1,1-dimethylethyl)-pheno;2,6-Bis(t-butyl)phenol;2,6-Bis(tert-butyl)phenol;2,6-Dibutylphenol;2,6-di-butylphenol;2,6-di-tert-butyl-pheno;2DTBP | CAS: | 128-39-2 | MF: | C14H22O | MW: | 206.32 | EINECS: | 204-884-0 | Product Categories: | Industrial/Fine Chemicals;Organic Building Blocks;Oxygen Compounds;Phenols;Building Blocks;C9 to C20+;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds | Mol File: | 128-39-2.mol | |
| 2,6-Di-tert-butylphenol Chemical Properties |
mp | 34-37 °C(lit.)
| bp | 253 °C(lit.)
| density | 0.91 | vapor pressure | <0.01 mm Hg ( 20 °C)
| refractive index | 1.5312 | Fp | 245 °F
| storage temp. | 2-8°C | Water Solubility | insoluble | BRN | 1841887 | Stability: | Stable. Incompatible with acid chlorides, acid anhydrides, bases, brass, copper, copper alloys, oxidizing agents. | CAS DataBase Reference | 128-39-2(CAS DataBase Reference) | NIST Chemistry Reference | Phenol, 2,6-bis(1,1-dimethylethyl)-(128-39-2) | EPA Substance Registry System | Phenol, 2,6-bis(1,1-dimethylethyl)- (128-39-2) |
| 2,6-Di-tert-butylphenol Usage And Synthesis |
Chemical Properties | white solid | General Description | Odorless colorless to light yellow solid or liquid. Floats on water. Freezing point is 97°F. | Air & Water Reactions | Insoluble in water. | Reactivity Profile | Phenols, such as 2,6-Di-tert-butylphenol, 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. | Health Hazard | Irritates eyes and (on prolonged contact) skin. Ingestion causes irritation of mouth and stomach. |
| 2,6-Di-tert-butylphenol Preparation Products And Raw materials |
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