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Sigma-Aldrich

N-Benzyl-N-methylethanolamine

technical grade, 90%

Synonym(s):

2-(N-Benzyl-N-methylamino)ethanol

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About This Item

Linear Formula:
C6H5CH2N(CH3)CH2CH2OH
CAS Number:
101-98-4
Molecular Weight:
165.23
EC Number:
202-994-3
MDL number:
MFCD00002847
UNSPSC Code:
12352100
PubChem Substance ID:
24862653
NACRES:
NA.22

grade

technical grade

assay

90%

form

liquid

refractive index

n20/D 1.529 (lit.)

bp

95-105 °C/2 mmHg (lit.)

density

1.017 g/mL at 25 °C (lit.)

SMILES string

CN(CCO)Cc1ccccc1

InChI

1S/C10H15NO/c1-11(7-8-12)9-10-5-3-2-4-6-10/h2-6,12H,7-9H2,1H3

InChI key

WOUANPHGFPAJCA-UHFFFAOYSA-N

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General description

N-Benzyl-N-methylethanolamine is a tertiary benzylamine. Electrochemical alkoxylation of N-benzyl-N-methylethanolamine is reported. Rate of proton exchange of N-benzyl-N-methylethanolamine in aqueous HCl has been reported.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Proton exchange mechanisms of some tertiary benzylamines.
Leyden DE and Morgan WR.
The Journal of Physical Chemistry, 73(9), 2924-2929 (1969)
The Anodic Oxidation of Organic Compounds. II. The Electrochemical Alkoxylation of Tertiary Amines.
Weinberg NL and Brown EA.
The Journal of Organic Chemistry, 31(12), 4058-4061 (1966)
Jessica Paul et al.
Journal of chromatography. A, 1366, 38-44 (2014-10-02)
In 2000 the implementation of quality by design (QbD) was introduced by the Food and Drug Administration (FDA) and described in the ICH Q8, Q9 and Q10 guidelines. Since that time, systematic optimization strategies for purification of biopharmaceuticals have gained

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