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ChemicalBook >> CAS DataBase List >> 2,6-Di-tert-butyl-4-methylphenol

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

CAS No.128-37-0
Chemical Name:2,6-Di-tert-butyl-4-methylphenol
Synonyms:p21;BHT;ao29;ao4k;BUKS;cao1;cao3;DBMP;P 21;DBPC
CBNumber:CB8355755
Molecular Formula:C15H24O
Formula Weight:220.35
MOL File:128-37-0.mol
2,6-Di-tert-butyl-4-methylphenol Property
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
Hazard Codes : Xn,N
Risk Statements : 22-36/37/38-36/38-50/53
Safety Statements : 26-36-37/39-61-60
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 Chemical Properties,Usage,Production

Chemical Properties
white crystalline solid
Usage
Antioxidant 264 as general antioxidants is used widely in polymer materials, petroleum products and food processing industries. Antioxidant 264 is commonly used rubber antioxidant, heat, oxygen aging have some protective effect, but also can inhibit copper harm. This product does not change color, not pollution. Antioxidants 264 high solubility in oil, no precipitation, less volatile, non-toxic and non-corrosive.
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.
2,6-Di-tert-butyl-4-methylphenol Preparation Products And Raw materials
Raw materials
Etanol 2-Methyl-1-propanol Column plate Phosphorous acid ISOBUTYLENE tert-Butanol p-Cresol Dehydrolyzing agent Sodium hydroxide
Preparation Products
2-tert-Butyl-4-methylphenol
2,6-Di-tert-butyl-4-methylphenol Suppliers      Global( 413)Suppliers     
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128-37-0(2,6-Di-tert-butyl-4-methylphenol)Related Search:
Potassium sorbate 2-Nitro-p-cresol N-ISOPROPYL-N-PHENYL-P-PHENYLENEDIAMINE 2,6-Di-tert-butyl-4-methylphenol 4,4'-Thiobis(6-tert-butyl-m-cresol) Poly(1,2-dihydro-2,2,4-trimethylquinoline) 2-tert-Butyl-4-methylphenol Pentaerythritol tetrakis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate) Bromocresol green N,N'-Di-2-naphthyl-p-phenylenediamine 2,6-Dinitro-p-cresol 2-Mercaptobenzimidazole Cresol Buprofezin Antioxidant BLE 2,4-Di-tert-butylphenol O,O'-Dioctadecylpentaerythritol bis(phosphite) 3-Ethylphenol
butyleret hydroxytoluen(= 2,6-di-tert-butyl-p-cresol) 2,6-Di-tert-butyl-4-methylphenol, 99.8% CH33C2C6H2CH3OH 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 BUTYLATEDHYDROXYTOLUENE,GRANULAR,NF di-tert-butylhydroxytoluene HOC6H2CH3C4H92 C4H92C6H2CH3OH Industrial/Fine Chemicals 2,6-DITERTIARY-BUTYL-4-METHYL-PHENOL(BHT) Butylated hydroxytoluene (BHT&2,6-DBPC) DI-TERT-BUTYL-PARA-CRESOL 2,6-DITERTIARYBUTYLPARACRESOL BHT (DI-TERT.-BUTYL-4-HYDROXYTOLUOL) "ionol" cp-antioxidant 2,6-Ditertbutyl-4-methyl phenol[128,37,0] 128370 BHT 2,6 - DI - TERT - BUTYL -4- METHYL PHENOL Aromatic Hydrocarbons (substituted) & Derivatives 2,6,-DI-TERT-BUTYL-4-METHYLPHENOL CP 2,6-DI-TERT-BUTYL-4-METHYLPHENOL, FOOD GRADE 99+% 2C6D2CH3OD Antioxidant Biochemistry BUTYLATED HYDROXYTOLUENE (BHT) FCC GRADE BUTYLATED HYDROXYTOLUENE (BHT) N.F. GRADE BUTYLATED HYDROXYTOLUENE pure 2,6-Di-tert-butyl-4-methylphenol, 2,6-Di-tert-butyl-p-cresol, BHT, Butylated hydroxytoluene, Butylhydroxytoluene, DBPC 2,6-Di-tert-butyl-p-cresol, BHT, Butylated hydroxytoluene, Butylhydroxytoluene, Butylhydroxytoluenum, DBPC 2,6-Di-tert-butyl-p-cresol, BHT, Butylated hydroxytoluene, Butylhydroxytoluene, DBPC RALOX(R) BT-45 "ionol"cp-antioxidant[qr] 1-Hydroxy-4-methyl-2,6-di-tert-butylbenzene 2,6-bis(1,1-dimethylethyl)-4-methyl-pheno 2,6-bis(1,1-dimethylethyl)-4-methylphenol[qr] 2,6-Bis(tert-butyl)-4-methylphenol 2,6-di- 2,6-di-butylcresol 2,6-di-Butyl-para-cresol 2,6-Di-terc.butyl-p-kresol 2,6-di-terc.butyl-p-kresol(czech) 2,6-Di-tert.-butyl-p-kresol 2,6-di-tert-butyl 2,6-Di-tert-butyl-1-hydroxy-methyl benzene 2,6-Di-tert-butyl-4-cresol 2,6-di-tert-butyl-4-hydroxytoluene 2,6-Di-tert-butylcresol 2,6-Di-tert-butylmethylphenol 2,6-di-tert-Butyl-methylphenol 2,6-Di-tert-butyl-para-cresol, food grade 2,6-di-tert-butyl-p-creso 2,6-Di-tert-butyl-p-cresol, food grade 2,6-Di-tert-butyl-p-methylphenol
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