2,6-Di-tert-butylphenol suppliers

2,6-Di-tert-butylphenol

CAS:: 128-39-2

MF:: C14H22O

MW:: 206.32

SecurityInformation

Symbol(GHS) ：: GHS07,GHS09

Signal word ：: Warning

Hazard statements ：: H315-H410

Precautionary statements ：: P264-P273-P280-P302+P352-P332+P313-P362+P364

Hazard Codes ：: Xn,N,Xi

Risk Statements ：: 22-51/53-52/53-50/53-38

Safety Statements ：: 26-36-61-29-60

RIDADR ：: UN 3145 8/PG 3

WGK Germany ：: 2

RTECS ：: SK8265000

TSCA ：: Yes

HazardClass ：: 9

PackingGroup ：: III

HS Code ：: 29071900

Use：: 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.

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Xiamen Eagle Chemical Limited Corporation