Tris(2-carboxyethyl) Isocyanurate - ≥98%(T) , CAS No.2904-41-8

CAS: 2904-41-8 Cat. No.: T162477 Molecular Weight: 345.26 EC Number: 220-803-1 PubChem CID: 73121
AVAILABLE TO ORDER
GRADE & PURITY ≥98%(T)
Synonyms
AS-48223 | Oprea1_160115 | 2,4,6-Trioxo-1,3,5-triazine-1,3,5(2H,4H,6H)-tripropanoic acid | F19825 | MLS000713969 | 1-(Cyclohexylamino)-2-propanol benzoate (ester) | 1,3,5-Triazine-1,3,5(2H,4H,6H)-tripropanoic acid, 2,4,6-trioxo- | SCHEMBL113643 | Tris(2-c
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5g
T162477-5g
10
$13.90
25g
T162477-25g
4
$37.90
100g
T162477-100g
1
$119.90
Enter a quantity for the sizes you want to add.
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Why this grade

≥98%(T) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
AS-48223 | Oprea1_160115 | 2, 4, 6-Trioxo-1, 3, 5-triazine-1, 3, 5(2H, 4H, 6H)-tripropanoic acid | F19825 | MLS000713969 | 1-(Cyclohexylamino)-2-propanol benzoate (ester) | 1, 3, 5-Triazine-1, 3, 5(2H, 4H, 6H)-tripropanoic acid, 2, 4, 6-trioxo- | SCHEMBL113643 | Tris(2-c
Specifications & Purity
≥98%(T)
Storage
Room temperature
Shipped In
Normal
Purity
≥98%(T)
Names and Identifiers
Pubchem Sid488184757
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488184757
Canonical SmilesC(CN1C(=O)N(C(=O)N(C1=O)CCC(=O)O)CCC(=O)O)C(=O)O
IUPAC Name3-[3,5-bis(2-carboxyethyl)-2,4,6-trioxo-1,3,5-triazinan-1-yl]propanoic acid
InChIKeyHENCHDCLZDQGIQ-UHFFFAOYSA-N
INCHI1S/C12H15N3O9/c16-7(17)1-4-13-10(22)14(5-2-8(18)19)12(24)15(11(13)23)6-3-9(20)21/h1-6H2,(H,16,17)(H,18,19)(H,20,21)
Isomeric SMILES C(CN1C(=O)N(C(=O)N(C1=O)CCC(=O)O)CCC(=O)O)C(=O)O
PubChem CID 73121
Molecular Weight 345.26
Reaxy-Rn 632220

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
SubclassTricarboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentTricarboxylic acids and derivatives
Alternative Parents Triazinones  1,3,5-triazines  Heteroaromatic compounds  Ureas  Carboxylic acids  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Tricarboxylic acid or derivatives - Triazinone - Triazine - 1,3,5-triazine - Heteroaromatic compound - Urea - Carboxylic acid - Azacycle - Organoheterocyclic compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TGR Thioredoxin glutathione reductase (28579 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

10 results found

Lot NumberCertificate TypeDateItem
E2613509Certificate of AnalysisApr 22, 2026 T162477
E2613522Certificate of AnalysisApr 22, 2026 T162477
A1815091Certificate of AnalysisSep 16, 2025 T162477
L2418436Certificate of AnalysisDec 10, 2024 T162477
L2418437Certificate of AnalysisDec 10, 2024 T162477
L2418438Certificate of AnalysisDec 10, 2024 T162477
J2429071Certificate of AnalysisNov 02, 2024 T162477
E2306693Certificate of AnalysisSep 15, 2022 T162477
J2231036Certificate of AnalysisSep 15, 2022 T162477
J2231050Certificate of AnalysisSep 15, 2022 T162477
Chemical and Physical Properties
Melt Point(°C)228 °C
Molecular Weight345.260 g/mol
XLogP3-2.100
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count9
Rotatable Bond Count9
Exact Mass345.081 Da
Monoisotopic Mass345.081 Da
Topological Polar Surface Area173.000 Ų
Heavy Atom Count24
Formal Charge0
Complexity483.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Solution Calculators
Reviews

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