1,5-Diaminopentane - ≥98% , CAS No.462-94-2

CAS: 462-94-2 Cat. No.: D121817 Fórmula: NH₂(CH₂)₅NH₂ Peso molecular: 102.18 Beilstein Registry Number: 1697256 Número CE: 207-329-0

GRADE & PURITY ≥98%

Synonyms

BioDex 1- | EC 207-329-0 | UNII-L90BEN6OLL | 1,5-pentanediamine | AI3-26937 | Pentane-1,5-diamine | BBL027704 | CCG-266036 | L90BEN6OLL | MFCD00008239 | Cadaverin | 1,5-Diaminopentane | 1,5-diamino-pentane | cadaverine | DTXSID5075448 | 4-04-00-01310 (Bei

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice,FedEx DG Service

Visão geral

Cadaverine is a biogenic amine. Mechanism of cadaverine fermentation by Corynebacterium glutamicum was reported. Cadaverine, a diamine, has been reported as a cadaveric volatile organic compound. Its effect on the electroantennographic (EAG) and behavioral responses of silphine species, Thanatophilus sinuatus Fabricius has been investigated. 

Application：

Cadaverine has been used as diamine in the synthesis of diamine-inorganic anion [Cl-, SO42-, HPO42-, P2O74- and Fe(CN)64-] complexes

Specifications

Sinónimos

BioDex 1- | EC 207-329-0 | UNII-L90BEN6OLL | 1,5-pentanediamine | AI3-26937 | Pentane-1,5-diamine | BBL027704 | CCG-266036 | L90BEN6OLL | MFCD00008239 | Cadaverin | 1,5-Diaminopentane | 1,5-diamino-pentane | cadaverine | DTXSID5075448 | 4-04-00-01310 (Bei

Especificações e pureza

≥98%

Condições de armazenamento de armazenamento

Store at 2-8°C,Argon charged

Enviado em

Wet ice,FedEx DG Service

Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.

Pureza

≥98%

Nomes e identificadores

Pubchem Sid

508807108

Sorrisos canónicos

C(CCN)CCN

IUPAC Name

pentane-1,5-diamine

InChIKey

VHRGRCVQAFMJIZ-UHFFFAOYSA-N

INCHI

1S/C5H14N2/c6-4-2-1-3-5-7/h1-7H2

SMILES isoméricas

C(CCN)CCN

WGK Alemanha

3

RTECS

SA0200000

Número UN

2735

Grupo de embalagem

III

Peso molecular

102.18

Beilstein

1697256

Reaxy-Rn

1697256

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1697256&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Classe Organonitrogen compounds
      • Subclass Amines
        • Level5 Primary amines
          • Level6 Monoalkylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Classe: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Primary amines
• Direct Parent: Monoalkylamines
• Alternative Parents: Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organopnictogen compound - Hydrocarbon derivative - Primary aliphatic amine - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as monoalkylamines. These are organic compounds containing an primary aliphatic amine group.
• External Descriptors: an aliphatic α,ω-diamine

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

Alvos associados (humanos)

CA5A Tclin Carbonic anhydrase 5A, mitochondrial (1 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA5B Tclin Carbonic anhydrase 5B, mitochondrial (1 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA6 Tclin Carbonic anhydrase 6 (1 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA3 Tclin Carbonic anhydrase 3 (1 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA4 Tclin Carbonic anhydrase 4 (1 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA12 Tclin Carbonic anhydrase 12 (1 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA14 Tclin Carbonic anhydrase 14 (1 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA9 Tclin Carbonic anhydrase 9 (1 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA7 Tclin Carbonic anhydrase 7 (1 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

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

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)

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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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Alvos associados (não humanos)

Ca7 Carbonic anhydrase VII (3 Activities)

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

Ca13 Carbonic anhydrase XIII (322 Activities)

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CA4 Carbonic anhydrase IV (1713 Activities)

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Mycobacterium tuberculosis (203094 Activities)

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Plasmodium falciparum (966862 Activities)

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J774 (3120 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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Ca15 Carbonic anhydrase 15 (173 Activities)

Discover Target: Ca15

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Mecanismos de ação

Propriedades químicas e físicas

• Solubilidade: Soluble in water.
• Sensibilidade: Air & Moisture Sensitive
• Índice de refração: 1.4585
• Ponto de inflamação (°F): 143.6 °F
• Ponto de inflamação (°C): 62 °C
• Ponto de ebulição (°C): 180°C
• Ponto de fusão (°C): 9.34°C
• Peso molecular: 102.180 g/mol
• XLogP3: -0.600
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 102.116 Da
• Monoisotopic Mass: 102.116 Da
• Topological Polar Surface Area: 52.000 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 25.300
• 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