Malonaldehyde bis(phenylimine) monohydrochloride - ≥95% , CAS No.123071-42-1

CAS: 123071-42-1 Cat. No.: M349130 Molecular Weight: 258.75

GRADE & PURITY ≥95%

Synonyms

Malonaldehyde Dianilide Hydrochloride | MFCD00054634 | N1,n3-diphenylpropane-1,3-diimine xhydrochloride | N,N'-diphenylpropane-1,3-diimine;hydrochloride | malonaldehyde bis(phenylimine)monohydrochloride | SCHEMBL2960053 | E77655 | N1,N3-DIPHENYLPROPANE-1,

Storage

Room temperature,Argon charged

Shipped In

Normal

Overview

Malonaldehyde bis(phenylimine) monohydrochloride is a useful fluorescent cyanine dye.

Specifications

Synonyms

Malonaldehyde Dianilide Hydrochloride | MFCD00054634 | N1, n3-diphenylpropane-1, 3-diimine xhydrochloride | N, N'-diphenylpropane-1, 3-diimine;hydrochloride | malonaldehyde bis(phenylimine)monohydrochloride | SCHEMBL2960053 | E77655 | N1, N3-DIPHENYLPROPANE-1,

Specifications & Purity

≥95%

Storage

Room temperature, Argon charged

Shipped In

Normal

Purity

≥95%

Names and Identifiers

• Pubchem Sid: 488197953
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488197953
• Canonical Smiles: C1=CC=C(C=C1)N=CCC=NC2=CC=CC=C2.Cl
• IUPAC Name: N,N'-diphenylpropane-1,3-diimine;hydrochloride
• InChIKey: FLMLOZWXXPLHIE-UHFFFAOYSA-N
• INCHI: 1S/C15H14N2.ClH/c1-3-8-14(9-4-1)16-12-7-13-17-15-10-5-2-6-11-15;/h1-6,8-13H,7H2;1H
• Isomeric SMILES: C1=CC=C(C=C1)N=CCC=NC2=CC=CC=C2.Cl
• WGK Germany: 3
• Molecular Weight: 258.75
• Reaxy-Rn: 3597716
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3597716&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Class Benzene and substituted derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzene and substituted derivatives
• Alternative Parents: Shiff bases Propargyl-type 1,3-dipolar organic compounds Hydrochlorides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Monocyclic benzene moiety - Shiff base - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Aldimine - Organic nitrogen compound - Hydrocarbon derivative - Hydrochloride - Organonitrogen compound - Imine - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
• 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

Chemical and Physical Properties

• Solubility: Soluble in water (partly).
• Sensitivity: Moisture sensitive
• Refractive Index: n20D~1.55 (Predicted)
• Melt Point(°C): 218° C (dec.)
• Molecular Weight: 258.740 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 258.092 Da
• Monoisotopic Mass: 258.092 Da
• Topological Polar Surface Area: 24.700 Ų
• Heavy Atom Count: 18
• Formal Charge: 0
• Complexity: 220.000
• 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: 2

XLogP3

References

1. Jie Zheng, Hao Ding, Lirong Bai, Shuai Zhu, Hongyuan Hui, Xinyue Zhu, Wen Chen, Aijun Hu.  (2023)  Microbial Succession and Flavor Changes During Fermentation of Semi-Dried Sea Bass (Lateolabrax maculatus).  Journal of Aquatic Food Product Technology,      [PMID:] [10.1080/10498850.2023.2258868]

2. Baihui Wang, Jingjing Luo, Qingling Zhang, Xing Cao, Yanjuan Zhang, Zuqiang Huang, Huayu Hu, Tao Gan.  (2023)  Storage of brown rice and its physicochemical properties under high temperature and humidity negative air ions environment.  JOURNAL OF CEREAL SCIENCE,      [PMID:] [10.1016/j.jcs.2023.103723]

3. Jinxi Feng, Tiantian Zhang, Jingxiang Sun, Jinzhu Zhu, Wen Yan, Shuanghong Tian, Ya Xiong.  (2021)  Improvement of sewage sludge dewatering by piezoelectric effect driven directly with pressure from pressure filtration: Towards understanding piezo-dewatering mechanism.  WATER RESEARCH,      [PMID:34890911] [10.1016/j.watres.2021.117922]

4. Zhaoxia Yang, Sasa Liu, Jing Lv, Zeping Sun, Wenhuan Xu, Chaofan Ji, Huipeng Liang, Shengjie Li, Chenxu Yu, Xinping Lin.  (2020)  Microbial succession and the changes of flavor and aroma in Chouguiyu, a traditional Chinese fermented fish.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2020.100725]

5. Yilin Lin, Xie Xuan, Kabore Manegdebwaoga Arthur Fabrice, Yigang Yu, Lihua Huang, Yehui Zhang.  (2025)  Effects of alkaline water-assisted tea polyphenol soaking on the physicochemical, biochemical, bacterial structure, and free amino acid composition of grass carp fillets during storage at 4 °C.  FOOD CONTROL,      [PMID:] [10.1016/j.foodcont.2025.111249]

6. Yanlan Ma, Xinyi Yang, Zongshuai Zhu, Tianran Huang, Jichao Huang, Ming Huang.  (2024)  Study on the stability, functional activity and preservation effect of oregano essential oil Pickering emulsion with different proportions of chicken bone gelatin/bacterial cellulose during storage.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:39515717] [10.1016/j.ijbiomac.2024.137309]

7. Yue Hu, Yangyi Yu, Jingxiang Sun, Wen Yan, Hanya Xie, Ya Xiong, Shuanghong Tian, Jinxi Feng.  (2025)  Catalytic conditioning and mechanism of sludge with a green conditioner MgO(110): The first example of boosting sludge conditioning by facet engineering.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2025.119555]

8. Hong Pan, Qi Luo, Qiuyi Jing, Lin Chen, Ni Li, Chao Fang, Fuguo Shi.  (2025)  Multiple endogenous aldehydes amplify acetaminophen-induced liver injury.  CHEMICO-BIOLOGICAL INTERACTIONS,      [PMID:40562332] [10.1016/j.cbi.2025.111619]