Dietilentriamina - ≥97% , CAS No.111-40-0

CAS: 111-40-0 Cat. No.: D100058 Fórmula: C₄H₁₃N₃ Peso molecular: 103.17 Beilstein Registry Number: 605314 Número EC: 203-865-4

CALIDAD & PUREZA ≥97%

Synonyms

DIETILENETRIAMINA|111-40-0|Bis(2-aminoetil)amina|2,2'-Diaminodietilamina|Dietilentriamina|1,4,7-Triazaheptano|Barsamida 115|Epicure T|Ancamina DETA|2,2'-Iminodietilamina|Aminoetiletiandiamina|N,N-Bis(2-aminoetil)amina|DETA|3-Azapentano-1,5-diamin

Storage

Temperatura ambiente, cargado con argón

Shipped In

FedEx DG Service

Especificaciones

Sinónimos

DIETILENETRIAMINA | 111-40-0 | Bis(2-aminoetil)amina | 2,2'-Diaminodietilamina | Dietilentriamina | 1,4,7-Triazaheptano | Barsamida 115 | Epicure T | Ancamina DETA | 2,2'-Iminodietilamina | Aminoetiletiandiamina | N,N-Bis(2-aminoetil)amina | DETA | 3-Azapentano-1,5-diamin

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Temperatura ambiente, cargado con argón

Enviado en

FedEx DG Service

Pureza

≥97%

Product Line

D100058-25ml

Nombres e identificadores

Pubchem Sid

508812067

Sonrisas canónicas

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

Isómeros SMILES

C(CNCCN)N

WGK Alemania

1

RTECS

IE1225000

Número ONU

2079

Grupo de embalaje

II

Peso molecular

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
    • Clase Organonitrogen compounds
      • Subclass Amines
        • Level5 Secondary amines
          • Level6 Dialkylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: 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
• Descripción: 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

Objetivos asociados (humanos)

CA2 Tclin Carbonic anhydrase II (17698 Activities)

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

VDR Tclin Vitamin D receptor (26531 Activities)

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

CA3 Tclin Carbonic anhydrase III (753 Activities)

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

CA6 Tclin Carbonic anhydrase VI (993 Activities)

Discover Target: CA6

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

CA1 Tclin Carbonic anhydrase I (13240 Activities)

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

CA5B Tclin Carbonic anhydrase VB (957 Activities)

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

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)

Discover Target: POLK

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

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

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

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

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

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

Objetivos asociados (no humanos)

Ca7 Carbonic anhydrase VII (3 Activities)

Discover Target: Ca7

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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)

Discover Target: Mmp9

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Luciferin 4-monooxygenase (66902 Activities)

Explore this target

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

Ca15 Carbonic anhydrase 15 (173 Activities)

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ddn Putative uncharacterized protein (49 Activities)

Discover Target: ddn

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

Discover Target: fba

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

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Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in water and ethanol, insoluble in ether.
• Sensibilidad: Air Sensitive
• Índice de refracción: 1.484
• Punto de inflamación (°F): 201.2 °F - closed cup
• Punto de inflamación (°C): 102 °C
• Punto de ebullición (°C): 199-209°C
• Punto de fusión (°C): -35°C
• Peso molecular: 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