Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

Safety Information

138339

Sigma-Aldrich

N-(2-Hydroxyethyl)phthalimide

99%

Synonym(s):

2-Phthalimidoethanol

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

About This Item

Empirical Formula (Hill Notation):
C10H9NO3
CAS Number:
3891-07-4
Molecular Weight:
191.18
Beilstein:
147214
EC Number:
223-434-4
MDL number:
MFCD00005903
UNSPSC Code:
12352100
PubChem Substance ID:
24848353
NACRES:
NA.22

Assay

99%

form

solid

mp

126-128 °C (lit.)

functional group

hydroxyl
imide

SMILES string

OCCN1C(=O)c2ccccc2C1=O

InChI

1S/C10H9NO3/c12-6-5-11-9(13)7-3-1-2-4-8(7)10(11)14/h1-4,12H,5-6H2

InChI key

MWFLUYFYHANMCM-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

N-(2-Hydroxyethyl)phthalimide is the precursor for chloromethyl ethers used in the synthesis of purine acyclic nucleosides.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

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

138339-25G:
138339-100G:
138339-BULK:
138339-VAR:

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BGBC5413V
MKBT5883V
MKBR7355V
MKBJ5796V
MKBH5813V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

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 1

1 of 1

2-Chloroethylamine hydrochloride 99%

Sigma-Aldrich

C40200

2-Chloroethylamine hydrochloride

J L Kelley et al.
Journal of medicinal chemistry, 24(12), 1528-1531 (1981-12-01)
A number of nitrogen analogues of 9-[(2-hydroxyethoxy)methyl]guanine [acylovir, Zovirax] containing amine functions in the side chain were synthesized and tested for antiviral activity. These purine acyclic nucleosides were prepared by reaction of tris(trimethylsilyl)guanine or 2,6-diaminopurine sodium salt with the chloromethyl
Molluscicidal activity of synthetic derivatives of 2-hydroxyethylphthalimide.
J N Lopes et al.
Revista brasileira de biologia, 40(3), 635-637 (1980-08-01)
Xuanrong Guo et al.
Biomacromolecules, 20(9), 3464-3474 (2019-07-25)
We report the design of reactive and hydrolytically degradable multilayers by the covalent layer-by-layer assembly of an azlactone-containing polymer, poly(2-vinyl-4,4-dimethylazlactone), with an acid-degradable, acetal-containing, small-molecule diamine linker. This approach yields cross-linked multilayers that contain (i) residual azlactone reactivity that can

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