3-dimethylaminobenzyl alcohol

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Names

[ CAS No. ]:
23501-93-1

[ 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

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...


More Articles


Related Compounds

  • 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
  • 2-(3-(allyloxy)phenyl)-7-bromo-3H-chromeno[2,3-d]pyrimidin-4(5H)-one
  • N-[(4-tert-butylphenyl)methyl]-3-[4,6-dimethyl-2-(methylsulfanyl)pyrimidin-5-yl]-N-methylpropanamide
  • 3-Butyl-2-methylbenzoic acid
  • N-({imidazo[1,2-a]pyridin-2-yl}methyl)-4-phenoxybenzene-1-sulfonamide
  • 2-fluoro-N-({8-methylimidazo[1,2-a]pyridin-2-yl}methyl)benzene-1-sulfonamide
  • 2-(3,4-dimethoxyphenyl)-N-(3-(thiazolo[5,4-b]pyridin-2-yl)phenyl)acetamide
  • 2-(3,4-Dimethoxyphenyl)-N-(2-methyl-3-{[1,3]thiazolo[5,4-B]pyridin-2-YL}phenyl)acetamide
  • N1-(2-morpholinoethyl)-N2-(2-(4-phenylpiperazin-1-yl)-2-(pyridin-3-yl)ethyl)oxalamide
  • 2-Fluoro-3-(pyridin-2-yl)pyridine
  • 1-[(1-Methyl-1H-pyrazol-4-yl)methyl]-L-proline
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