Skip to Content
Merck
All Photos(2)

Documents

Safety Information

528331

Sigma-Aldrich

N-Methyl-N-(2-hydroxyethyl)-4-aminobenzaldehyde

96%

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
(HOCH2CH2)(CH3)NC6H4CHO
CAS Number:
1201-91-8
Molecular Weight:
179.22
MDL number:
MFCD00963547
UNSPSC Code:
12352100
PubChem Substance ID:
24877578
NACRES:
NA.22

Assay

96%

mp

66-70 °C (lit.)

SMILES string

CN(CCO)c1ccc(C=O)cc1

InChI

1S/C10H13NO2/c1-11(6-7-12)10-4-2-9(8-13)3-5-10/h2-5,8,12H,6-7H2,1H3

InChI key

JOCUIVLSLBBESN-UHFFFAOYSA-N

Related Categories

Application

N-Methyl-N-(2-hydroxyethyl)-4-aminobenzaldehyde may be used to synthesize:
  • 2,5-bis[4-(methylaminoethanol)benzylidene]cyclopentanone
  • 4′-[(2-tosyloxyethyl)(methyl)amino]-4-phenyl-3-buten-2-malonitrile, a tosylate precursor
  • methanesulfonic acid 2-[(4-formyl-phenyl)-methyl-amino]-ethyl ester

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

528331-25G:
528331-BULK:
528331-VAR:

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 2

1 of 2

Tetrabutylammonium fluoride solution 1.0 M in THF

Sigma-Aldrich

216143

Tetrabutylammonium fluoride solution

p-Anisaldehyde 98%

Sigma-Aldrich

A88107

p-Anisaldehyde

Synthesis and characterization of dendritic nonlinear optical chromophore containing phenylene attached with bulky alkyl group.
Choi JJ, et al.
Macromolecular Research, 15(1), 59-64 (2007)
18F-FBM: A new PET radiotracer for imaging ?-amyloid plaques and neurofibrillary tangles.
Wang C, et al.
Journal of Nuclear Medicine, 47(1), 217P-217P (2006)
Waqas Ahmad et al.
Chemical biology & drug design, 83(6), 670-681 (2014-01-11)
Arachidonic acid and its metabolites have generated a heightened interest due to their significant role in inflammation. Inhibiting the enzymes involved in arachidonic acid metabolism has been considered as the synergistic anti-inflammatory effect. A series of novel curcumin diarylpentanoid analogues

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service