Diethylenetriamine - ≥99% , CAS No.111-40-0

CAS: 111-40-0 Cat. No.: D100059 Formula: C₄H₁₃N₃ Peso molecolare: 103.17 Beilstein Registry Number: 605314 Numero EC: 203-865-4

QUALITÀ & PUREZZA ≥99%

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

Specifiche

Sinonimi

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.

Specifiche e purezza

≥99%

Condizioni di conservazione di stoccaggio

Room temperature,Argon charged,Desiccated

Spedito in

FedEx DG Service

Purezza

≥99%

Product Line

D100059-100ml

Nomi e identificatori

Pubchem Sid

508812066

Sorrisi canonici

C(CNCCN)N

IUPAC Name

N'-(2-aminoethyl)ethane-1,2-diamine

InChIKey

RPNUMPOLZDHAAY-UHFFFAOYSA-N

INCHI

1S/C4H13N3/c5-1-3-7-4-2-6/h7H,1-6H2

Isomeri SMILES

C(CNCCN)N

WGK Germania

1

RTECS

IE1225000

Numero UN

2079

Gruppo di imballaggio

II

Peso molecolare

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=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Classe Organonitrogen compounds
      • Subclass Amines
        • Level5 Secondary amines
          • Level6 Dialkylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Classe: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Secondary amines
• Direct Parent: Dialkylamines
• Alternative Parents: Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Secondary aliphatic amine - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Primary aliphatic amine - Aliphatic acyclic compound
• Descrizione: This 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

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

Obiettivi associati (umani)

CA2 Tclin Carbonic anhydrase II (17698 Activities)

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VDR Tclin Vitamin D receptor (26531 Activities)

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CA3 Tclin Carbonic anhydrase III (753 Activities)

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CA6 Tclin Carbonic anhydrase VI (993 Activities)

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CA1 Tclin Carbonic anhydrase I (13240 Activities)

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CA5B Tclin Carbonic anhydrase VB (957 Activities)

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CA5A Tclin Carbonic anhydrase VA (1168 Activities)

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CA14 Tclin Carbonic anhydrase XIV (1305 Activities)

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CA12 Tclin Carbonic anhydrase XII (6231 Activities)

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CA9 Tclin Carbonic anhydrase IX (8255 Activities)

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POLK Tbio DNA polymerase kappa (8653 Activities)

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APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)

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RECQL Tbio ATP-dependent DNA helicase Q1 (5575 Activities)

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MEN1 Tchem Menin/Histone-lysine N-methyltransferase MLL (48157 Activities)

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Obiettivi associati (non umani)

Ca7 Carbonic anhydrase VII (3 Activities)

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Ca13 Carbonic anhydrase XIII (322 Activities)

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CA4 Carbonic anhydrase IV (1713 Activities)

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Mmp9 Matrix metalloproteinase 9 (38 Activities)

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Luciferin 4-monooxygenase (66902 Activities)

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Ca15 Carbonic anhydrase 15 (173 Activities)

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ddn Putative uncharacterized protein (49 Activities)

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fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)

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ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)

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Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in water, benzene, ethanol, acetone and methanol, insoluble in ether and n-heptane
• Sensibilità: Moisture & Air sensitive.
• Indice di rifrazione: 1.484
• Punto di infiammabilità (°F): 201.2 °F - closed cup
• Punto di infiammabilità (°C): 102 °C
• Punto di ebollizione (°C): 199-209°C
• Punto di fusione (°C): -35°C
• Peso molecolare: 103.170 g/mol
• XLogP3: -2.100
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 103.111 Da
• Monoisotopic Mass: 103.111 Da
• Topological Polar Surface Area: 64.099 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 26.100
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1