Dimethylaminopropylamine
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Names | |
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Preferred IUPAC name
N1,N1-Dimethylpropane-1,3-diamine | |
Other names
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Identifiers | |
3D model (JSmol)
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ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.003.347 ![]() |
EC Number |
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MeSH | 3-dimethylaminopropylamine |
PubChem CID
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RTECS number |
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UNII | |
UN number | 2733 |
CompTox Dashboard (EPA)
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Properties | |
C5H14N2 | |
Molar mass | 102.181 g·mol−1 |
Appearance | Colourless liquid |
Odor | fishy, ammoniacal |
Density | 812 mg mL−1 |
Boiling point | 132.1 °C; 269.7 °F; 405.2 K |
log P | −0.211 |
Vapor pressure | 0.7–2.4 kPa |
Refractive index (nD)
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1.435–1.436 |
Thermochemistry | |
Heat capacity (C)
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255.7 J K−1 mol−1 |
Std molar
entropy (S |
323.0 J K−1 mol−1 |
Std enthalpy of
formation (ΔfH⦵298) |
−76.9–−76.9 kJ mol−1 |
Std enthalpy of
combustion (ΔcH⦵298) |
−3.8955–−3.8875 MJ mol−1 |
Hazards | |
GHS labelling: | |
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Signal word
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Danger |
H226, H302, H314, H317 | |
P280, P305+P351+P338, P310 | |
Flash point | 32 °C (90 °F; 305 K) |
Explosive limits | 2.3–12.36% |
Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
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Related compounds | |
Related amines
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Related compounds
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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Infobox references | |
Dimethylaminopropylamine (DMAPA) is a diamine used in the preparation of some surfactants, such as cocamidopropyl betaine which is an ingredient in many personal care products including soaps, shampoos, and cosmetics. BASF, a major producer, claims that DMAPA-derivatives do not sting the eyes and makes a fine-bubble foam, making it appropriate in shampoos.[1]
Preparation and reactions[]
DMAPA is commonly produced commercially via the reaction between dimethylamine and acrylonitrile (a Michael reaction) to produce dimethylaminopropionitrile. A subsequent hydrogenation step yields DMAPA:[2]
DMAPA is readily converted to the mustard dimethylaminopropyl-3-chloride, a powerful alkylating agent.[3]
Health effects[]
Dimethylaminopropylamine is a known skin irritant and its presence as an impurity in cocamidopropyl betaine is thought to be the cause of irritation experienced by some individuals.[4][5]
See also[]
References[]
- ^ "BASF ups capacity at DMAPA plant". Cosmetics Design. 2003-10-28.
- ^ 3-Aminopropyldimethylamine (PDF). OECD Screening Information Dataset. UN Environment.
- ^ Loeliger, P.; Flückiger, E. (1976). "Sulfide Contraction via Alkylative Coupling: 3-Methyl-2,4-Hepthanedione". Organic Syntheses. 55: 127. doi:10.15227/orgsyn.055.0127.
- ^ Angelini, Gianni; Foti, Caterina; Rigano, Luigi; Vena, Gino A. (February 1995). "3-Dimethylaminopropylamine: a key substance in contact allergy to cocamidopropylbetaine?". Contact Dermatitis. 32 (2): 96–99. doi:10.1111/j.1600-0536.1995.tb00754.x.
- ^ PIGATTO, P (March 1995). "Contact dermatitis to cocamidopropylbetaine is caused by residual amines: Relevance, clinical characteristics, and review of the literature". American Journal of Contact Dermatitis. 6 (1): 13–16. doi:10.1016/1046-199X(95)90062-4.
- Diamines
- Dimethylamino compounds