17383
Benzene-1,3,5-triacetic acid
≥97.0% (T)
Synonym(s):
1,3,5-Tris(carboxymethyl)benzene
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C12H12O6
CAS Number:
Molecular Weight:
252.22
Beilstein:
9300288
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
≥97.0% (T)
form
powder
SMILES string
OC(=O)Cc1cc(CC(O)=O)cc(CC(O)=O)c1
InChI
1S/C12H12O6/c13-10(14)4-7-1-8(5-11(15)16)3-9(2-7)6-12(17)18/h1-3H,4-6H2,(H,13,14)(H,15,16)(H,17,18)
InChI key
AJEIBHNKBLRDNT-UHFFFAOYSA-N
Other Notes
Building block and core molecule for generating diverse libraries in combinatorial chemistry; preparation of giant propeller molecules
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2
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
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.
Customers Also Viewed
L. Tong et al.
Journal of the American Chemical Society, 119, 7291-7291 (1997)
S. Brandl et al.
J. Prakt. Chem., 338, 451-451 (1996)
J.S. Bradshaw et al.
Journal of Heterocyclic Chemistry, 35, 519-519 (1998)
T Carell et al.
Chemistry & biology, 2(3), 171-183 (1995-03-01)
The increasing interest in combinatorial chemistry as a tool for the development of therapeutics has led to many new methods of creating molecular libraries of potential lead compounds. Current methods have made it possible to develop libraries of several million
Tomohisa Sawada et al.
Nature communications, 10(1), 5687-5687 (2019-12-14)
Cavity creation is a key to the origin of biological functions. Small cavities such as enzyme pockets are created simply through liner peptide folding. Nature can create much larger cavities by threading and entangling large peptide rings, as learned from
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