Dimethylamine Hydroiodide - ≥98%(N)(T) , CAS No.51066-74-1

CAS: 51066-74-1 Cat. No.: D155610 Molecular Weight: 173.00 EC Number: 256-945-6

GRADE & PURITY ≥98%(N)(T)

Synonyms

DTXSID20965349 | dimethylazanium iodide | BCA06674 | dimethylamine hydroiodide | EINECS 256-945-6 | AS-57984 | N-Methylmethanamine--hydrogen iodide (1/1) | N-methylmethanamine;hydroiodide | SY117064 | MFCD28100829 | Dimethylammonium iodide | dimethylamine

Storage

Room temperature,Argon charged,Cool

Shipped In

Normal

Overview

Product Application：

Dimethylammonium iodide (DMAI) is used as an additive for the fabrication of perovskite-based solar cells. It improves the crystal phases and morphologies of the perovskite films, which affect the power conversion efficiency (PCE) of the optoelectronic devices.

Specifications

Synonyms

DTXSID20965349 | dimethylazanium iodide | BCA06674 | dimethylamine hydroiodide | EINECS 256-945-6 | AS-57984 | N-Methylmethanamine--hydrogen iodide (1/1) | N-methylmethanamine;hydroiodide | SY117064 | MFCD28100829 | Dimethylammonium iodide | dimethylamine

Specifications & Purity

≥98%(N)(T)

Storage

Room temperature, Argon charged, Cool

Shipped In

Normal

Purity

≥98%(N)(T)

Names and Identifiers

• Pubchem Sid: 488197930
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488197930
• Canonical Smiles: CNC.I
• IUPAC Name: N-methylmethanamine;hydroiodide
• InChIKey: JMXLWMIFDJCGBV-UHFFFAOYSA-N
• INCHI: 1S/C2H7N.HI/c1-3-2;/h3H,1-2H3;1H
• Isomeric SMILES: CNC.I
• Molecular Weight: 173.00
• Reaxy-Rn: 3939587
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3939587&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Class Organonitrogen compounds
      • Subclass Quaternary ammonium salts

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Class: Organonitrogen compounds
• Subclass: Quaternary ammonium salts
• Intermediate Tree Nodes: Not available
• Direct Parent: Quaternary ammonium salts
• Alternative Parents: Dialkylamines Organic iodide salts Hydrocarbon derivatives Organic cations
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Quaternary ammonium salt - Secondary aliphatic amine - Hydrocarbon derivative - Organic iodide salt - Organic salt - Amine - Organic cation - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as quaternary ammonium salts. These are compounds containing positively charged polyatomic ion of the structure NR4+, R being an alkyl group or an aryl group.
• 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: Light & Air & Moisture Sensitive
• Melt Point(°C): 155 °C
• Molecular Weight: 173.000 g/mol
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 172.97 Da
• Monoisotopic Mass: 172.97 Da
• Topological Polar Surface Area: 12.000 Ų
• Heavy Atom Count: 4
• Formal Charge: 0
• Complexity: 2.800
• 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

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