| Identification | More | [Name]
1-(Dimethylamino)tetradecane | [CAS]
112-75-4 | [Synonyms]
1-(DIMETHYLAMINO)TETRADECANE
MYRISTYL DIMETHYLAMINE
N,N-DIMETHYLMYRISTYLAMINE
N,N-DIMETHYL-N-TETRADECYLAMINE
N,N-DIMETHYLTETRADECYLAMINE
TETRADECYLDIMETHYLAMINE
Adma 14
Armeen DM 14D
armeendm14d
Armine DM14D
Dimethyl myristamine
dimethyl(tetradecyl)amine
dimethylmyristamine
dimethylmyristylamine
Dimethyl-n-tetradecylamine
Dimethyltetradecylamine
dimethyl-tetradecyl-amine
Empigen AH
n,n-dimethyl-1-tetradecanamin
N,N-Dimethyl-1-tetradecanamine | [EINECS(EC#)]
204-002-4 | [Molecular Formula]
C16H35N | [MDL Number]
MFCD00053736 | [Molecular Weight]
241.46 | [MOL File]
112-75-4.mol |
| Chemical Properties | Back Directory | [Definition]
A liquidcationic detergent; acid stable. | [Appearance]
Liquid | [Melting point ]
-3°C | [Boiling point ]
148 °C / 2mmHg | [density ]
0.795 g/mL at 20 °C(lit.)
| [vapor pressure ]
0.02-9.4Pa at 20-50℃ | [refractive index ]
n20/D 1.441
| [Fp ]
131 °C | [storage temp. ]
Room Temperature | [solubility ]
Chloroform (Slightly), Hexane (Slightly), Methanol (Slightly) | [form ]
Oil | [pka]
9.78±0.28(Predicted) | [color ]
Clear Colourless | [Usage]
Barlene(R) tertiary amines are used as chemical intermediates for the manufacture of quaternary ammonium compounds, amine oxide and betaine surfactants | [BRN ]
1748246 | [LogP]
1.3-6.91 at 20℃ and pH7.1-8.8 | [Surface tension]
25.2-26.5mN/m at 1g/L and 25℃ | [Dissociation constant]
9.78 at 25℃ | [CAS DataBase Reference]
112-75-4(CAS DataBase Reference) | [NIST Chemistry Reference]
1-Tetradecanamine, n,n-dimethyl-(112-75-4) | [EPA Substance Registry System]
112-75-4(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
C | [Risk Statements ]
R22:Harmful if swallowed.
R34:Causes burns. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . | [RIDADR ]
UN 2735 8/PG 3
| [WGK Germany ]
3
| [F ]
10-34 | [HS Code ]
2921.19.6190 | [HazardClass ]
8 | [PackingGroup ]
III | [Hazardous Substances Data]
112-75-4(Hazardous Substances Data) |
| Hazard Information | Back Directory | [General Description]
A light yellow liquid with a fishlike odor. Insoluble in water and less dense than water. Hence floats on water. Contact may irritate skin, eyes and mucous membranes. May be toxic by ingestion, inhalation or skin absorption. Used to make other chemicals. | [Reactivity Profile]
DIMETHYLTETRADECANAMINE neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides. | [Air & Water Reactions]
Insoluble in water. | [Health Hazard]
TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution. | [Fire Hazard]
Combustible material: may burn but does not ignite readily. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form. | [Chemical Properties]
Liquid | [Uses]
N,N-Dimethyltetradecylamine has been used for the synthesis of 1,6-bis(N,N-tetradecyl dimethylammonium adipate), a counterion coupled gemini (cocogem) surfactant.
It may also be used in the following studies:
- For the isolation of recombinant botulinum neurotoxin fragments in the yeast Pichia pastoris by cell permeabilization method.
- Synthesis of gemini surfactants belonging to the series of alkanediyl-α,ω-bis-(dimethylalkyl ammonium bromide, which were evaluated as corrosion inhibitors of iron in hydrochloric acid medium.
- Preparation of cationic gemini surfactant of the type N-alkanediyl 1,2-ethane bis(dimethyl ammonium bromide).
| [Uses]
Barlene(R) tertiary amines are used as chemical intermediates for the manufacture of quaternary ammonium compounds, amine oxide and betaine surfactants | [Uses]
N,N-Dimethyltetradecylamine (cas# 112-75-4) is a compound useful in organic synthesis. |
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