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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
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.)
functional group
amine
hydroxyl
phenyl
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.
Signal Word
Warning
Hazard Statements
Precautionary 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
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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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