Succinic Dihydrazide - ≥97%(HPLC)(T) , CAS No.4146-43-4

CAS: 4146-43-4 Cat. No.: S161141 Peso molecular: 146.15 Beilstein Registry Number: 2(4)1925 Número EC: 223-970-9 PubChem CID: 72491

GRADE & PURITY ≥97%(HPLC)(T)

Synonyms

Succinoyldihydrazine | BBL035998 | butanedihydrazide | C4H10N4O2 | EINECS 223-970-9 | MFCD00007613 | Succinic dihydrazide;Butanedioyl dihydrazide | Succinyl dihydrazide | NSC 29540 | Butanedioyl dihydrazide | E81949 | NSC 25180 | NSC 42940 | Succinhydrazi

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

Succinoyldihydrazine | BBL035998 | butanedihydrazide | C4H10N4O2 | EINECS 223-970-9 | MFCD00007613 | Succinic dihydrazide;Butanedioyl dihydrazide | Succinyl dihydrazide | NSC 29540 | Butanedioyl dihydrazide | E81949 | NSC 25180 | NSC 42940 | Succinhydrazi

Especificaciones y pureza

≥97%(HPLC)(T)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥97%(HPLC)(T)

Nombres e identificadores

• Pubchem Sid: 488184694
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488184694
• Sonrisas canónicas: C(CC(=O)NN)C(=O)NN
• IUPAC Name: butanedihydrazide
• InChIKey: HCOMFAYPHBFMKU-UHFFFAOYSA-N
• INCHI: 1S/C4H10N4O2/c5-7-3(9)1-2-4(10)8-6/h1-2,5-6H2,(H,7,9)(H,8,10)
• Isómeros SMILES: C(CC(=O)NN)C(=O)NN
• WGK Alemania: 3
• RTECS: WM7500000
• PubChem CID: 72491
• Peso molecular: 146.15
• Beilstein: 2(4)1925
• Reaxy-Rn: 1775110

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acid hydrazides
• Alternative Parents: Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Carboxylic acid hydrazide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as carboxylic acid hydrazides. These are carboxylic acid derivatives containing a carbonyl group in which the carbon is directly linked to a hydrazide group (N-N).
• External Descriptors: Not available

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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in water; Degree of Solubility in water: 340 g/l 25 °C
• Sensibilidad: Air Sensitive
• Punto de fusión (°C): 168°C(lit.)
• Peso molecular: 146.150 g/mol
• XLogP3: -2.800
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 146.08 Da
• Monoisotopic Mass: 146.08 Da
• Topological Polar Surface Area: 110.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 119.000
• 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

Referencias

1. Bengang Li, Xin Tian, Xuzhi Cao, Zhenyang Luo.  (2023)  Antiswelling and robust supramolecular polyurea hydrogels induced by the synergy of hydrogen bond and hydrophobic interaction for constructing durable underwater anti-oil-fouling coatings.  JOURNAL OF APPLIED POLYMER SCIENCE,  141  (6): (e54920).  [PMID:] [10.1002/app.54920]

2. Li-Hong Su, Hai-Long Qian, Shu-Ting Xu, Cheng Yang, Zhenyu Wang, Xiu-Ping Yan.  (2025)  Designing flexible aliphatic linker based molecular imprinted covalent organic framework for rapid and selective extraction and detection of trace zearalenone.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:40037192] [10.1016/j.jhazmat.2025.137778]

3. Qi Zhang, Ruibing Lv, Ying Wang, Zhenghang Luo, Pengyang Pan, Tingwei Wang, Quancheng Liu.  (2024)  Energetic copper(II) quadridentate chelate: a novel green laser-sensitive primary explosive.  Inorganic Chemistry Frontiers,  11  (11): (3168-3177).  [PMID:] [10.1039/D4QI00489B]

4. Jingya Zhao, Huiqing Zhu, Tenglong Xu, Suyue Xu, Yuxin Wang, Yanwei Hou, Meng Zhuo, Kun Du, Yingyu Su, Xiao Han, Yongli Shi, Xueyan Hou.  (2025)  Self-Healing Oxidized Dextran/Sodium Alginate Hydrogel Dressing with Hemostatic Activity Speeds Up Wound Healing in Burn Injuries.  ACS Applied Materials & Interfaces,      [PMID:39763399] [10.1021/acsami.4c16333]

5. Guowen Zhou, Yunfeng Zhou, Xiaoqian Zhang, Zepeng Lei, Xiaohui Wang.  (2025)  High-strength, self-healable, transparent castor-oil-based waterborne polyurethane barrier coatings enabled by a dynamic acylhydrazone co-monomer.  GREEN CHEMISTRY,  27  (8): (2220-2229).  [PMID:] [10.1039/D4GC06103A]

6. Lihong Su, Luliang Wang, Lei Zhao, Yushen Liu, Chengke Wang, Chen Shao, Lu Liu, Daohong Zhang, Ibrahim A. Darwish.  (2025)  Tailoring flexible aliphatic covalent organic frameworks with hydroxyl sites: A novel platform for efficient extraction and rapid detection of bisphenols.  TALANTA,      [PMID:41252909] [10.1016/j.talanta.2025.129134]