N,N,N',N'-Tetrakis(2-hydroxypropyl)ethylenediamine - ≥98% , CAS No.102-60-3

CAS: 102-60-3 Cat. No.: T121820 Molecular Weight: 292.41 Beilstein Registry Number: 4(4)1685 EC Number: 203-041-4

GRADE & PURITY ≥98%

Synonyms

Quadrol | 1,1',1'',1'''-(Ethylenedinitrilo)tetra-2-propanol | Ethylenediamine-N,N,N',N'-tetra-2-propanol

Storage

Argon charged,Room temperature

Shipped In

Normal

Overview

Application

N,N,N',N'-Tetrakis(2-hydroxypropyl)ethylenediamine is used as a catalyst in the production of urethane foams. It acts as a complexing agent, plasticizer, surfactant solubilizer and curing agent for epoxy resin. It is also used as a viscosity modifier and as an anti-bloating agent for cattle. It is utilized in piezoelectric crystal detectors of sulfur dioxide and in additives for paint. It serves as a biological buffer as well as reagent for manganese. Further, it finds application in adhesives and sealant chemicals. In addition to this, it is used as a cross-linking agent.

Specifications

Synonyms

Quadrol | 1, 1', 1'', 1'''-(Ethylenedinitrilo)tetra-2-propanol | Ethylenediamine-N, N, N', N'-tetra-2-propanol

Specifications & Purity

≥98%

Storage

Argon charged, Room temperature

Shipped In

Normal

Action Type

ACTIVATOR

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488180504
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488180504
• Canonical Smiles: CC(CN(CCN(CC(C)O)CC(C)O)CC(C)O)O
• IUPAC Name: 1-[2-[bis(2-hydroxypropyl)amino]ethyl-(2-hydroxypropyl)amino]propan-2-ol
• InChIKey: NSOXQYCFHDMMGV-UHFFFAOYSA-N
• INCHI: 1S/C14H32N2O4/c1-11(17)7-15(8-12(2)18)5-6-16(9-13(3)19)10-14(4)20/h11-14,17-20H,5-10H2,1-4H3
• Isomeric SMILES: CC(CN(CCN(CC(C)O)CC(C)O)CC(C)O)O
• WGK Germany: 3
• RTECS: UB5604000
• Molecular Weight: 292.41
• Beilstein: 4(4)1685
• Reaxy-Rn: 1781143

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Class Organonitrogen compounds
      • Subclass Amines
        • Level5 Alkanolamines
          • Level6 1,2-aminoalcohols

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Class: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Alkanolamines
• Direct Parent: 1,2-aminoalcohols
• Alternative Parents: Trialkylamines Secondary alcohols Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - 1,2-aminoalcohol - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as 1,2-aminoalcohols. These are organic compounds containing an alkyl chain with an amine group bound to the C1 atom and an alcohol group bound to the C2 atom.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

GLS Tchem Glutaminase kidney isoform, mitochondrial (16997 Activities)

Discover Target: GLS

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)

Discover Target: ffp

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Chemical and Physical Properties

• Solubility: Miscible with water, methanol, ethanol, toluene, ethylene glycol and perchloroethylene.
• Sensitivity: Air Sensitive
• Refractive Index: 1.4795-1.4815
• Flash Point(°F): 411.8 °F
• Flash Point(°C): 211 °C
• Boil Point(°C): 190°C
• Molecular Weight: 292.410 g/mol
• XLogP3: -0.700
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 11
• Exact Mass: 292.236 Da
• Monoisotopic Mass: 292.236 Da
• Topological Polar Surface Area: 87.400 Ų
• Heavy Atom Count: 20
• Formal Charge: 0
• Complexity: 199.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 4
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

1. Liping Zhi, Tianyu Li, Xiaoqi Liu, Zhizhang Yuan, Xianfeng Li.  (2022)  Functional complexed zincate ions enable dendrite-free long cycle alkaline zinc-based flow batteries.  Nano Energy,      [PMID:] [10.1016/j.nanoen.2022.107697]

2. Qili Yu, Qunfu Fan, Wenzheng Chen, Yujie Chen, Chengzhen Du, Guangqiang Fang, Yuxuan Wu, Hezhou Liu.  (2024)  Thermal responsive polyurethane/brominated isobutylene isoprene rubber co-continuous IPNs elastomer: From tunable shape memory behavior to high damping properties.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.155410]

3. Si Yejia, Sun Zhuo, Zhao Qian, Xie Tao, Wu Jingjun.  (2025)  3D printing of salt-like granular polyacrylamide as sacrificial molds for shaping versatile materials.  Nature Communications,  16  (1): (1-10).  [PMID:40764489] [10.1038/s41467-025-62674-1]