1,5-Diaminopentane Dihydrochloride - ≥98% , CAS No.1476-39-7

CAS: 1476-39-7 Cat. No.: D111805 Peso molecular: 175.10 Beilstein Registry Number: 3611329 Número EC: 216-022-0

GRADE & PURITY ≥98%

Synonyms

Cadaverine dihydrochloride, ~98% | CHEBI:64701 | 1,5-Pentanediamine dihydrochloride | G 641 | NSC 129885 | Cadaverine dihydrochloride, >=99.0% (AT) | FGNLEIGUMSBZQP-UHFFFAOYSA-N | Pentamethylenediamine Hydrochloride | D0099 | Pentamethylenediamine dihydro

Storage

Room temperature,Argon charged

Shipped In

Normal

Specifications

Sinónimos

Cadaverine dihydrochloride, ~98% | CHEBI:64701 | 1, 5-Pentanediamine dihydrochloride | G 641 | NSC 129885 | Cadaverine dihydrochloride, >=99.0% (AT) | FGNLEIGUMSBZQP-UHFFFAOYSA-N | Pentamethylenediamine Hydrochloride | D0099 | Pentamethylenediamine dihydro

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature, Argon charged

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504755454
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504755454
• Sonrisas canónicas: C(CCN)CCN.Cl.Cl
• IUPAC Name: pentane-1,5-diamine;dihydrochloride
• InChIKey: FGNLEIGUMSBZQP-UHFFFAOYSA-N
• INCHI: 1S/C5H14N2.2ClH/c6-4-2-1-3-5-7;;/h1-7H2;2*1H
• Isómeros SMILES: C(CCN)CCN.Cl.Cl
• WGK Alemania: 3
• Peso molecular: 175.10
• Beilstein: 3611329
• Reaxy-Rn: 3611329

Taxonomic Classification

Taxonomy Tree

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

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

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

Propiedades químicas y físicas

• Sensibilidad: Moisture sensitive
• Punto de fusión (°C): 260-262°C
• Peso molecular: 175.100 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 174.069 Da
• Monoisotopic Mass: 174.069 Da
• Topological Polar Surface Area: 52.000 Ų
• Heavy Atom Count: 9
• 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: 3

XLogP3

Referencias

1. Shijin Xiong, Xiaoyan Xu, Qiaozhen Liu, Yazhou Xu, Hongbing Ren, Tao Xiong, Mingyong Xie.  (2023)  Integrated metatranscriptomics and metabolomics revealed the metabolic pathways of biogenic amines during Laotan Suancai fermentation.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2023.103517]

2. Furong Jin, Xinyue Yin, Yang Wan, Jiukai Zhang, Jindi Wang, Xiangbo Fu, Tianxin Fu, Buwei Liu, Yongshi Chen, Bo Tian, Zhibiao Feng.  (2023)  Ultrasonic–microwave synergistic supramolecular solvent liquid–liquid microextraction of trace biogenic amines in fish and beer based on solidification of floating organic droplet.  FOOD CHEMISTRY,      [PMID:37516607] [10.1016/j.foodchem.2023.136965]

3. Xuan Qi, Wei-Feng Wang, Jun Wang, Jun-Li Yang, Yan-Ping Shi.  (2018)  Highly selective colorimetric detection of putrescine in fish products using o-phthalaldehyde derivatization reaction.  FOOD CHEMISTRY,      [PMID:29680050] [10.1016/j.foodchem.2018.03.131]

4. Jinxin Zheng, Xiaoju Liu, Yanpeng Xiong, Qingyin Meng, Peiyu Li, Fan Zhang, Xiaoming Liu, Zhiwei Lin, Qiwen Deng, Zewen Wen, Zhijian Yu.  (2024)  AMXT-1501 targets membrane phospholipids against Gram-positive and -negative multidrug-resistant bacteria.  Emerging Microbes & Infections,      [PMID:38422452] [10.1080/22221751.2024.2321981]

5. Yanan Liu, Yuhao Huang, Qileng Aori, Yu Wang, Sai Zhao, Zhen-Lin Xu.  (2026)  A sustained-release antibacterial gelatin hydrogel based on metal-phenolic networks for long-term preservation of prefabricated meat.  FOOD CHEMISTRY,      [PMID:] [10.1016/j.foodchem.2026.149080]