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TMEDA

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Identification
Molecular formula
C6H16N2
CAS number
110-18-9
IUPAC name
N,N,N',N'-tetramethylmethanediamine
State
State
TMEDA is a liquid at room temperature with an amine-like, fishy odor.
Melting point (Celsius)
-55.00
Melting point (Kelvin)
218.15
Boiling point (Celsius)
122.00
Boiling point (Kelvin)
395.15
General information
Molecular weight
116.22g/mol
Molar mass
116.2210g/mol
Density
0.7755g/cm3
Appearence

TMEDA is a colorless liquid with an amine-like odor.

Comment on solubility

Solubility of N,N,N',N'-tetramethylmethanediamine (C6H16N2)

N,N,N',N'-tetramethylmethanediamine is a diamine compound characterized by its moderate solubility properties. This organic molecule exhibits solubility in various solvents, primarily due to its polar amine functional groups. Here are some key points regarding its solubility:

  • Solubility in Water: The presence of amine groups typically enhances solubility in water, but due to its bulky structure and hydrophobic carbon chains, this compound may have limited solubility.
  • Solubility in Organic Solvents: N,N,N',N'-tetramethylmethanediamine is more readily soluble in non-polar and polar organic solvents, such as ethanol and acetone. This is due to its carbon backbone that interacts favorably with organic solvent structures.
  • Temperature Effects: Like many organic compounds, its solubility may increase with temperature, making higher temperatures a favorable condition for dissolving this compound.
  • Concentration Limits: As with many amines, its solubility is subject to concentration limits beyond which saturation occurs, affecting its usability in various chemical processes.

In summary, N,N,N',N'-tetramethylmethanediamine demonstrates moderate solubility characteristics, influenced by both its molecular structure and the nature of the solvent. It serves as a fascinating example of how functional groups can alter solubility behavior.

Interesting facts

Interesting Facts about N,N,N',N'-Tetramethylmethanediamine

N,N,N',N'-Tetramethylmethanediamine, often abbreviated as TMMD, is a fascinating compound with diverse applications in the field of chemistry and beyond. Here are some intriguing aspects of TMMD:

  • Structure and Function: TMMD features a unique structure where two secondary amine groups are attached to a central carbon atom. This specific configuration contributes to its reactivity and behavior in various chemical reactions.
  • Versatile Solvent: Due to its polar nature, TMMD is an excellent solvent for many organic compounds, making it invaluable in laboratory settings for synthesis and extraction processes.
  • Applications in Research: TMMD is frequently used in the synthesis of specialty chemicals and as a reagent in organic chemistry. Its capability to stabilize reaction intermediates is particularly noteworthy.
  • Role in Catalysis: This compound has been explored as a potential catalyst in several chemical reactions, enhancing the efficiency of processes such as polymerization and organic transformations.
  • Health and Safety: While TMMD plays a significant role in various industrial applications, it is crucial to handle it with care. Precautions should be taken to avoid inhalation or skin contact, as it may pose health risks.

As quoted by a leading chemist, “The versatility of compounds like TMMD showcases the incredible complexity and potential found in organic chemistry.” The study of such compounds not only enriches our understanding of chemical interactions but also paves the way for advances in materials science, pharmaceuticals, and beyond.

In summary, N,N,N',N'-tetramethylmethanediamine is more than just a simple compound; it is a gateway to discoveries and innovations in chemistry, demonstrating the significance of seemingly simple molecules in complex reactions.

Synonyms
51-80-9
N,N,N',N'-Tetramethylmethanediamine
N,N,N',N'-Tetramethyldiaminomethane
Bis(dimethylamino)methane
Tetramethylmethylenediamine
METHANEDIAMINE, N,N,N',N'-TETRAMETHYL-
Methylenebis(dimethylamine)
[(dimethylamino)methyl]dimethylamine
N,N,N',N'-Tetramethylmethylenediamine
NSC 166169
Methylenediamine, N,N,N',N'-tetramethyl-
Dimethyl((dimethylamino)methyl)amine
N,N,N',N'-Tetramethyldiaminomethan
102830-06-8
EINECS 200-124-7
UNII-Z870I525KS
AI3-26640
tetramethyldiaminomethane
Z870I525KS
N,N,N',N'-Tetramethyldiaminomethan [German]
NSC-54796
NSC-166169
TETRAMETHYLMETHANEDIAMINE
DTXSID1058761
2,4-dimethyl-2,4-diazapentane
EC 200-124-7
((CH3)2N)2CH2
Dimethyl[(dimethylamino)methyl]amine
NA 9069
Tetramethyl methylene diamine
N,N',N'-Tetramethyldiaminomethan
N,N',N'-Tetramethylmethanediamine
N,N',N'-Tetramethylmethylenediamine
WLN: 1N1&1N1&1
Methanediamine,N,N',N'-tetramethyl-
Methylenediamine,N,N',N'-tetramethyl-
N,N',N'-TETRAMETHYLDIAMINOMETHANE
MFCD00008328
n,n,n,n-tetramethyldiaminomethane
N,N,N,N-Tetramethylmethanediamine
2,4-Dimethyl-2,4-diazapentane; Bis(dimethylamino)methane; Dimethyl[(dimethylamino)methyl]amine; Methylenebis(dimethylamine)
NSC54796
bisdimethylaminomethane
Bis-dimethylaminomethane
bis-dimethylamino-methane
bis (dimethylamino)methane
bis-(dimethylamino)methane
bis-(dimethylamino)-methane
SCHEMBL64976
bis-(di-methylamino)-methane
DTXCID2040949
dimethylaminomethyl-dimethyl-amine
N,N,N',N'Tetramethyldiaminomethan
N,N,N',N'-tetramethydiaminomethane
N,N,N',N'Tetramethyldiaminomethane
N,N,N',N'Tetramethylmethanediamine
BBL027709
N,N,N',N'-tetramethyidiaminomethane
NSC166169
STL146737
AKOS000121074
Methanediamine, N,N,N',N'tetramethyl
N,N,N', N'-tetramethyldiaminomethane
N,N,N',N',-tetramethyldiaminomethane
AT28827
Methylenediamine, N,N,N',N'tetramethyl
N,N,N',N'-Tetramethyl-methane diamine
VS-08582
DB-052031
N,N,N',N'-Tetramethyldiaminomethane, 99%
NS00008200
T0969
EN300-23836
N,N,N\',N\'-TETRAMETHYLDIAMINOMETHANE
Q27295126
F0001-1334
N pound notN pound notN' pound notN'-TETRAMETHYLDIAMINOMETHANE