Diethanolamine Hydrochloride - ≥95%(T) , CAS No.14426-21-2

CAS: 14426-21-2 Cat. No.: D155708 Molecular Weight: 141.6 EC Number: 238-396-4

GRADE & PURITY ≥95%(T)

Synonyms

Diethanolamine hydrochloride, 98% | SY102019 | DIETHANOLAMINE HYDROCHLORIC ACID SALT | AS-66121 | Diethanolamine hydrochloride | DECYLGALLATE | VJLOFJZWUDZJBX-UHFFFAOYSA-N | E75801 | DTXSID10884752 | SCHEMBL1011320 | Ethanol, 2,2'-iminobis-, hydrochloride

Storage

Room temperature,Argon charged

Shipped In

Normal

Overview

Diethanolamine hydrochloride was used in the synthesis of: . N-monophenylpiperazine . diethanolammonium chloride, required for the preparation of diethanolammonium-tetrachloridopalladate(II) complex

Specifications

Synonyms

Diethanolamine hydrochloride, 98% | SY102019 | DIETHANOLAMINE HYDROCHLORIC ACID SALT | AS-66121 | Diethanolamine hydrochloride | DECYLGALLATE | VJLOFJZWUDZJBX-UHFFFAOYSA-N | E75801 | DTXSID10884752 | SCHEMBL1011320 | Ethanol, 2, 2'-iminobis-, hydrochloride

Specifications & Purity

≥95%(T)

Storage

Room temperature, Argon charged

Shipped In

Normal

Purity

≥95%(T)

Names and Identifiers

• Pubchem Sid: 488189999
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488189999
• Canonical Smiles: C(CO)NCCO.Cl
• IUPAC Name: 2-(2-hydroxyethylamino)ethanol;hydrochloride
• InChIKey: VJLOFJZWUDZJBX-UHFFFAOYSA-N
• INCHI: 1S/C4H11NO2.ClH/c6-3-1-5-2-4-7;/h5-7H,1-4H2;1H
• Isomeric SMILES: C(CO)NCCO.Cl
• WGK Germany: 1
• RTECS: KL3500000
• Molecular Weight: 141.6
• Reaxy-Rn: 3613277
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3613277&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Class Organonitrogen compounds
      • Subclass Amines
        • Level5 Alkanolamines
          • Level6 1,2-aminoalcohols

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Class: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Alkanolamines
• Direct Parent: 1,2-aminoalcohols
• Alternative Parents: Dialkylamines Primary alcohols Organopnictogen compounds Organic zwitterions Organic chloride salts Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: 1,2-aminoalcohol - Secondary amine - Secondary aliphatic amine - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organic chloride salt - Organic salt - Organic zwitterion - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as 1,2-aminoalcohols. These are organic compounds containing an alkyl chain with an amine group bound to the C1 atom and an alcohol group bound to the C2 atom.
• 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
• Sensitivity: Hygroscopic
• Refractive Index: 1.517
• Flash Point(°F): 235.4 °F
• Flash Point(°C): 113 °C
• Molecular Weight: 141.600 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 141.056 Da
• Monoisotopic Mass: 141.056 Da
• Topological Polar Surface Area: 52.500 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 28.900
• 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. Yaqi Yin, Chen Fan, Yuwei Shan, Linru Cheng.  (2023)  Fabrication of amorphous metal-organic framework in deep eutectic solvent for boosted organophosphorus pesticide adsorption.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2023.109963]

2. Naveed Ahmad, Xiaoxiao Wang, Peixu Sun, Ying Chen, Fahad Rehman, Jian Xu, Xia Xu.  (2021)  Electrochemical CO2 reduction to CO facilitated by MDEA-based deep eutectic solvent in aqueous solution.  RENEWABLE ENERGY,      [PMID:] [10.1016/j.renene.2021.05.106]

3. Wanlin Deng, Chen Fan, Ming Jin, Ruixue Zhang.  (2025)  Integrated deep eutectic solvent with amorphous metal–organic framework for highly sensitive electrochemical determination of dicofol in milk and water.  FOOD CHEMISTRY,      [PMID:40840391] [10.1016/j.foodchem.2025.145993]

4. Dongshun Deng, Xiaoxia Deng, Ke Li, Hao Fang.  (2021)  Protic ionic liquid ethanolamine thiocyanate with multiple sites for highly efficient NH3 uptake and NH3/CO2 separation.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2021.119298]