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366412

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:
Molecular Weight:
165.23
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

technical grade

Quality Level

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

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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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)
Proton exchange mechanisms of some tertiary benzylamines.
Leyden DE and Morgan WR.
The Journal of Physical Chemistry, 73(9), 2924-2929 (1969)
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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