Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

447854

Sigma-Aldrich

Diethyl 5-(hydroxymethyl)isophthalate

98%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
HOCH2C6H3-1,3-(CO2C2H5)2
CAS Number:
181425-91-2
Molecular Weight:
252.26
MDL number:
MFCD00239424
UNSPSC Code:
12352100
PubChem Substance ID:
24868368
NACRES:
NA.22

Quality Level

100

assay

98%

form

solid

mp

82-85 °C (lit.)

functional group

ester
hydroxyl

SMILES string

CCOC(=O)c1cc(CO)cc(c1)C(=O)OCC

InChI

1S/C13H16O5/c1-3-17-12(15)10-5-9(8-14)6-11(7-10)13(16)18-4-2/h5-7,14H,3-4,8H2,1-2H3

InChI key

AMRPMZYDTZVKTP-UHFFFAOYSA-N

Related Categories

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SHBB5754V
09129CH
14720AE
12928MD
19430DB

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

Stefan Raddatz et al.
Nucleic acids research, 30(21), 4793-4802 (2002-11-01)
We report the synthesis of new phosphoramidite building blocks and their use for the modification of oligonucleotides with hydrazides. The reaction of these hydrazide oligonucleotides with active esters and aldehydes is demonstrated for solution conjugation and immobilization. Compared with the
Surface adsorption of polar end-functionalised polystyrenes.
Narrainen AP, et al.
Soft Matter, 2(11), 981-985 (2006)
Hydrophobic derivatives of 5-(hydroxymethyl) isophthalic acid that selectively induce apoptosis in leukemia cells but not in fibroblasts.
Galkin A, et al.
Drug Development Research, 69(4), 185-195 (2008)
Gustav Boije af Gennäs et al.
Journal of medicinal chemistry, 52(13), 3969-3981 (2009-05-15)
Protein kinase C (PKC) is a widely studied molecular target for the treatment of cancer and other diseases. We have approached the issue of modifying PKC function by targeting the C1 domain in the regulatory region of the enzyme. Using

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