3-dimethylaminobenzyl alcohol

Suppliers

Names

[ Name ]:
3-dimethylaminobenzyl alcohol

[Synonym ]:
m-dimethylaminobenzyl alcohol
EINECS 245-700-9
MFCD00017342
m-NMe2-benzyl alcohol
(3-(Dimethylamino)phenyl)methanol
3-(Dimethylamino)benzyl alcohol

Chemical & Physical Properties

[ Density]:
1.056 g/mL at 25 °C(lit.)

[ Boiling Point ]:
282-283 °C(lit.)

[ Molecular Formula ]:
C₉H₁₃NO

[ Molecular Weight ]:
151.20600

[ Flash Point ]:
>230 °F

[ Exact Mass ]:
151.10000

[ PSA ]:
23.47000

[ LogP ]:
1.24490

[ Vapour Pressure ]:
0.00154mmHg at 25°C

[ Index of Refraction ]:
n20/D 1.577(lit.)

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

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

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2922199090

Synthetic Route

Click to get detail synthetic route

Customs

[ HS Code ]: 2922199090

[ Summary ]:
2922199090. other amino-alcohols, 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

Laccase-catalyzed mediated oxidation of benzyl alcohol: the role of TEMPO and formation of products including benzonitrile studied by nanoelectrospray ionization Fourier transform ion cyclotron resonance mass spectrometry.

J. Mass Spectrom. 39(10) , 1139-46, (2004)

Substituted benzyl alcohol was oxidized enzymatically with a laccase-mediator system and the products were investigated as a function of time by nanoelectrospray ionization Fourier transform ion cyclo...

α-(t-butylaminomethyl)-4-hydroxy-3-dimethylaminobenzyl alcohol
3-chloro-5-N,N-dimethylaminobenzyl alcohol
4-dimethylaminobenzyl alcohol
α-[(tert-butylamino)-methyl]3,5-dichloro-4-dimethylaminobenzyl alcohol
α,α-Bis(trifluoromethyl)-p-dimethylaminobenzyl alcohol
m-PEG4-(CH2)3-alcohol
ethyl 2-amino-4-(3-nitrophenyl)-5-oxo-4H,5H-thiochromeno[4,3-b]pyran-3-carboxylate
ethyl 2-amino-4-(4-nitrophenyl)-5-oxo-4H,5H-thiochromeno[4,3-b]pyran-3-carboxylate
ethyl 2-amino-4-(3-chloro-4-nitrophenyl)-5-oxo-4H,5H-thiochromeno[4,3-b]pyran-3-carboxylate
methyl 2-amino-4-(2,6-dichlorophenyl)-5-oxo-4H,5H-thiochromeno[4,3-b]pyran-3-carboxylate
tert-Butyl [1-(azidomethyl)cyclopropyl]carbamate
methyl 2-amino-4-(2-chloro-6-fluorophenyl)-5-oxo-4H,5H-thiochromeno[4,3-b]pyran-3-carboxylate
methyl 2-amino-4-(3-nitrophenyl)-5-oxo-4H,5H-thiochromeno[4,3-b]pyran-3-carboxylate
methyl 2-amino-4-(4-nitrophenyl)-5-oxo-4H,5H-thiochromeno[4,3-b]pyran-3-carboxylate
methyl 2-amino-4-(3-chloro-4-nitrophenyl)-5-oxo-4H,5H-thiochromeno[4,3-b]pyran-3-carboxylate
isopropyl 2-amino-4-(3-nitrophenyl)-5-oxo-4H,5H-thiochromeno[4,3-b]pyran-3-carboxylate

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