2,6-Di-tert-butyl-4...

2,6-Di-tert-butyl-4-methylphenol 128-37-0

2,6-Di-tert-butyl-4-methylphenol 128-37-0

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128-37-0 2,6-Di-tert-butyl-4-methylphenol C15H24O

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128-37-0     

2,6-Di-tert-butyl-4-methylphenol Basic information
Product Name: 2,6-Di-tert-butyl-4-methylphenol
Synonyms: butyleret hydroxytoluen(= 2,6-di-tert-butyl-p-cresol);2,6-Di-tert-butyl-4-methylphenol, 99.8%;2,6-Di-(tert-butyl)-4-methylphynol-D21;3,5-di-tert-4butylhydroxytoluene (bht);BHT (BAGS);BHT FCC/NF;BHT,GRANULAR,FCC;BHT,GRANULAR,TECHNICAL
CAS: 128-37-0
MF: C15H24O
MW: 220.35
EINECS: 204-881-4
Product Categories: Industrial/Fine Chemicals;Aromatic Hydrocarbons (substituted) & Derivatives;Antioxidant;Biochemistry;Aromatics;BHT
Mol File: 128-37-0.mol
 
 
2,6-Di-tert-butyl-4-methylphenol Chemical Properties
mp  69-73 °C(lit.)
bp  265 °C(lit.)
density  1.048
vapor density  7.6 (vs air)
vapor pressure  <0.01 mm Hg ( 20 °C)
FEMA  2184
refractive index  1.4859
Fp  127 °C
storage temp.  0-6°C
solubility  methanol: 0.1 g/mL, clear, colorless
Water Solubility  insoluble
Merck  14,1548
BRN  1911640
Stability: Stable, but light-sensitive. Incompatible with acid chlorides, acid anhydrides, brass, copper, copper alloys, steel, bases, oxidizing agents. Combustible.
CAS DataBase Reference 128-37-0(CAS DataBase Reference)
NIST Chemistry Reference Butylated hydroxytoluene(128-37-0)
EPA Substance Registry System Phenol, 2,6-bis(1,1-dimethylethyl)- 4-methyl-(128-37-0)
 
Safety Information
Hazard Codes  Xn
Risk Statements  22-36/37/38-36/38
Safety Statements  26-36-37/39
RIDADR  3077
WGK Germany  1
RTECS  GO7875000
F  8-10-23
HazardClass  9
PackingGroup  III
HS Code  29071900
Hazardous Substances Data 128-37-0(Hazardous Substances Data)
 
2,6-Di-tert-butyl-4-methylphenol Usage And Synthesis
Chemical Properties white crystalline solid
Usage antioxidant
General Description White crystalline solid.
Air & Water Reactions Insoluble in water.
Reactivity Profile Phenols, such as 2,6-Di-tert-butyl-4-methylphenol, 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. May react with oxidizing materials.
Fire Hazard 2,6-Di-tert-butyl-4-methylphenol is combustible.

 

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