2-Amino-4-tert-butylphenol

Names

[ Name ]:
2-Amino-4-tert-butylphenol

[Synonym ]:
amino-4-tert-butylphenol
2-amino-4-tert.-butyl-phenol
T-BUTYL-O-AMINOPHENOL
2-Amino-4-(2-methyl-2-propanyl)phenol
2-AMINO-4-T-BUTYLPHENOL
Phenol, 2-amino-4-(1,1-dimethylethyl)-
2-HYDROXY-5-TERT-BUTYLANILINE
MFCD00007698
4-tert-Butyl-2-aminophenol
2-Amino-4tertutyl plenol
2-Hydroxy-5-t-butylanilin
p-tert-Butyl-o-aminophenol
o-Amino-p-tert-butylphenol
2-Amino-4-(tert-butyl)phenol
EINECS 214-844-4
2-Amino-4-tert-butylphenol
2-hydroxy-5-tert-butyl-1-aminobenzene

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
274.9±33.0 °C at 760 mmHg

[ Melting Point ]:
160-163 °C(lit.)

[ Molecular Formula ]:
C₁₀H₁₅NO

[ Molecular Weight ]:
165.232

[ Flash Point ]:
120.1±25.4 °C

[ Exact Mass ]:
165.115356

[ PSA ]:
46.25000

[ LogP ]:
2.13

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.561

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302 + H312 + H332-H315-H319-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn:Harmful

[ Risk Phrases ]:
R20/21/22;R36/37/38

[ Safety Phrases ]:
S26-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ Packaging Group ]:
I; II; III

[ Hazard Class ]:
6.1

[ HS Code ]:
2922299090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2922299090

[ Summary ]:
2922299090. other amino-naphthols and other amino-phenols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Synthesis of 2-(2-, 3-, and 4-pyridyl) benzoxazoles by the reaction of phenolic Schiff bases with thianthrene cation radical. Park MS, et al.

J. Heterocycl. Chem. 39(6) , 1279-82, (2002)

Rationally designed 4-phenoxy substituted prolinamide phenols organocatalyst for the direct aldol reaction in water. Zhang S-P, et al.

Tetrahedron Lett. 50(11) , 1173-76, (2009)

Neutral anion receptors: synthesis and evaluation as sensing molecules in chemically modified field effect transistors. Antonisse MMG, et al.

J. Org. Chem. 62(26) , 9034-38, (1997)

Related Compounds

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.