Company Name: |
Hangzhou Sage Chemical Co., Ltd.
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Tel: |
+86057186818502 13588463833 |
Email: |
info@sagechem.com |
Products Intro: |
Product Name:Phenol, 3-(diMethylaMino)-4-Methyl- CAS:119-31-3 Purity:98% Package:1g;5g;100g;Bulk
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Company Name: |
Finetech Industry Limited
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Tel: |
027-87465837 19945049750 |
Email: |
sales@finetechnology-ind.com |
Products Intro: |
Product Name:3-(Dimethylamino)-4-methylphenol CAS:119-31-3 Purity:98% Package:1g;10g;25g;500g;1kg
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Company Name: |
MQ (shanghai) Pharmaceuticals Co., Ltd.
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Tel: |
13761635123 |
Email: |
1014988033@qq.com |
Products Intro: |
Product Name:Phenol, 3-(dimethylamino)-4-methyl- CAS:119-31-3 Purity:>95% Package:1G,5G
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| Phenol, 3-(dimethylamino)-4-methyl- Basic information |
| Phenol, 3-(dimethylamino)-4-methyl- Chemical Properties |
| Phenol, 3-(dimethylamino)-4-methyl- Usage And Synthesis |
General Description | Red liquid with phenolic odor. | Air & Water Reactions | Moderately soluble in water. | Reactivity Profile | Phenols, such as Phenol, 3-(dimethylamino)-4-methyl-, 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. | Fire Hazard | Flash point data for Phenol, 3-(dimethylamino)-4-methyl- are not available. Phenol, 3-(dimethylamino)-4-methyl- is probably combustible. |
| Phenol, 3-(dimethylamino)-4-methyl- Preparation Products And Raw materials |
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