Diethylenetriamine - ≥98.5% , CAS No.111-40-0

CAS: 111-40-0 Cat. No.: D301794 Formula: C4H13N3 Molecular Weight: 103.17 Beilstein Registry Number: 605314 EC Number: 203-865-4
AVAILABLE TO ORDER
GRADE & PURITY ≥98.5%
Synonyms
DETA | N-(2-Aminoethyl)ethylenediamine | n-(2-aminoethyl)-ethylenediamine | Tox21_201453 | 3-Aza-1,5-diaminopentane | J-520317 | Z104475186 | 2, 2'-Diaminodiethylamine | ChS-P 1 | NSC446 | NSC-446 | 2-(2-Aminoethylamino)ethylamine | Ancamine DETA | D.E.H.
Storage
Room temperature,Argon charged,Desiccated
Shipped In
FedEx DG Service
★
Size
Germany (EU)
USA*
Price
Qty
500g
D301794-500g
Made to order · 8–12 wks
€50.24
Enter a quantity for the sizes you want to add.
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Why this grade

≥98.5% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Argon charged,Desiccated Ships FedEx DG Service 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 467 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
DETA | N-(2-Aminoethyl)ethylenediamine | n-(2-aminoethyl)-ethylenediamine | Tox21_201453 | 3-Aza-1,5-diaminopentane | J-520317 | Z104475186 | 2, 2'-Diaminodiethylamine | ChS-P 1 | NSC446 | NSC-446 | 2-(2-Aminoethylamino)ethylamine | Ancamine DETA | D.E.H.
Specifications & Purity
≥98.5%
Legal Information
产品生产厂家:巴斯夫
Storage
Room temperature,Argon charged,Desiccated
Shipped In
FedEx DG Service
Purity
≥98.5%
Names and Identifiers
Pubchem Sid504751582
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504751582
Canonical SmilesC(CNCCN)N
IUPAC NameN'-(2-aminoethyl)ethane-1,2-diamine
InChIKeyRPNUMPOLZDHAAY-UHFFFAOYSA-N
INCHI1S/C4H13N3/c5-1-3-7-4-2-6/h7H,1-6H2
Isomeric SMILES C(CNCCN)N
WGK Germany 1
RTECS IE1225000
UN Number 2079
Packing Group II
Molecular Weight 103.17
Beilstein 605314
Reaxy-Rn 605314
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=605314&ln=

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 nitrogen compounds
ClassOrganonitrogen compounds
SubclassAmines
Intermediate Tree Nodes Secondary amines
Direct ParentDialkylamines
Alternative Parents Organopnictogen compounds  Monoalkylamines  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Secondary aliphatic amine - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Primary aliphatic amine - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as dialkylamines. These are organic compounds containing a dialkylamine group, characterized by two alkyl groups bonded to the amino nitrogen.
External Descriptors triamine - polyazaalkane
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA3 Tclin Carbonic anhydrase III (753 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA6 Tclin Carbonic anhydrase VI (993 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5B Tclin Carbonic anhydrase VB (957 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5A Tclin Carbonic anhydrase VA (1168 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA14 Tclin Carbonic anhydrase XIV (1305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA12 Tclin Carbonic anhydrase XII (6231 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA9 Tclin Carbonic anhydrase IX (8255 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLK Tbio DNA polymerase kappa (8653 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RECQL Tbio ATP-dependent DNA helicase Q1 (5575 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MEN1 Tchem Menin/Histone-lysine N-methyltransferase MLL (48157 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Ca7 Carbonic anhydrase VII (3 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca13 Carbonic anhydrase XIII (322 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA4 Carbonic anhydrase IV (1713 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mmp9 Matrix metalloproteinase 9 (38 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Luciferin 4-monooxygenase (66902 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca15 Carbonic anhydrase 15 (173 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ddn Putative uncharacterized protein (49 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ffp 4'-phosphopantetheinyl transferase ffp (24982 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.

15 results found

Lot NumberCertificate TypeDateItem
D2617088Certificate of AnalysisApr 29, 2026 D301794
E2607168Certificate of AnalysisApr 27, 2026 D301794
E2607169Certificate of AnalysisApr 27, 2026 D301794
E2607170Certificate of AnalysisApr 27, 2026 D301794
H2614019Certificate of AnalysisApr 27, 2026 D301794
B2525009Certificate of AnalysisFeb 07, 2025 D301794
E2319127Certificate of AnalysisMay 09, 2023 D301794
E2319128Certificate of AnalysisMay 09, 2023 D301794
E2319133Certificate of AnalysisMay 09, 2023 D301794
G2415348Certificate of AnalysisMay 09, 2023 D301794
J2312071Certificate of AnalysisMay 09, 2023 D301794
J2320058Certificate of AnalysisMay 09, 2023 D301794
K2224130Certificate of AnalysisNov 17, 2022 D301794
K2224131Certificate of AnalysisNov 17, 2022 D301794
K2224140Certificate of AnalysisNov 17, 2022 D301794
Chemical and Physical Properties
SensitivityMoisture & Air sensitive.
Refractive Index1.484
Flash Point(°F)201.2 °F - closed cup
Flash Point(°C)102 °C
Boil Point(°C)199-209°C
Melt Point(°C)-35°C
Molecular Weight103.170 g/mol
XLogP3-2.100
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count3
Rotatable Bond Count4
Exact Mass103.111 Da
Monoisotopic Mass103.111 Da
Topological Polar Surface Area64.099 Ų
Heavy Atom Count7
Formal Charge0
Complexity26.100
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
Documents & Articles
A Complete Guide to Selecting Epoxy Curing Systems: Amines vs. Anhydrides vs. Latent Curing — with Aladdin’s Recommended Selection Table
Formulation Design and Selection of Amine Curing Agents in Epoxy Systems
Understanding Amine Curing Agents: Structure, Types, and Application Selection
Analysis of the Epoxy Resin Curing Mechanism: From Ring-Opening Reaction, Gelation and Crosslinking to Post-Curing and Property Development
Fluorocarbon Resin Coating Formulation Design: Resin Selection, Supporting Systems, and Key Application Control Points
When Should You Choose Silicone Resin? Selection Comparison with Epoxy, Acrylic, Polyurethane, Fluororesin, and Other Coating Resins
Epoxy Phenolic Coatings: Why Are They Commonly Used for Chemical Resistance, Solvent Resistance, Heat Resistance, and Internal Metal Surface Protection?
Applicability Boundaries, Failure Risks, and Alternative System Selection for Chlorinated Rubber Resin in Coatings
Cashew Nut Shell Liquid (CNSL): From Cashew Processing By-Product to Reactive Bio-Based Raw Material for Coating Resins
Guide to Common Waterborne Resin Types and Application-Based Selection: How to Choose Acrylics, PUD, Waterborne Epoxy, Waterborne Alkyd, VAE, and Related Chemicals
From Water to Film: Film-Formation Mechanisms and Performance Development of Waterborne Emulsions and Dispersions
Mechanisms and Control of Coating Yellowing: From Chromophoric Structure Formation to Source Diagnosis and Formulation Optimization
Structural Design Logic of Common Resin Modification Technologies: Molecular Chain Structure, Functional Groups, Phase Structure, Crosslinked Networks, and Hybrid/Functional Design
Mechanism, Diagnosis, and Control of Coating Lifting: Solvent Penetration, Film Swelling, and Interlayer Instability
Resin Polarity in Coating Formulations: From Molecular Structure to Dissolution, Compatibility, Interfacial Interactions, and Formulation Design
What Are Polyamines? Structural Features, Classification and Representative Compounds, Applications, and Synthetic Strategies
Structure, Properties, and Mechanisms of Powdered Fragrances and Fragrance Delivery Materials: Stability, Release Mechanisms, and Selection Logic
Application of Conductive Carbon Black in Coatings: Selection Criteria, Dispersion Control, and Conductive Network Construction
Application of Aldimine Latent Curing Agents in One-Component Moisture-Curing Polyurethane Systems —— Mechanism of CO₂ Bubble Control and Key Formulation Design Points
Citations of This Product
Solution Calculators
Reviews

Customer Reviews

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