19059-68-8

Basic information

• Product Name: 3-DIMETHYLAMINO-2,2-DIMETHYL-1-PROPANOL
• Synonyms: DIMETHYLAMINONEOPENTANOL;3-DIMETHYLAMINO-2,2-DIMETHYL-1-PROPANOL;3-(dimethylamino)-2,2-dimethyl-1-propano;dimethylaminodimethylpropanol;3-(dimethylamino)-2,2-dimethylpropan-1-ol;3-Dimethylaminoneopentanol;3-DIMETHYLAMINO-2,2-DIMETHYL-1-PROPANOL 97+%
• CAS NO: 19059-68-8
• Molecular Formula: C₇H₁₇NO
• Molecular Weight: 131.22
• EINECS: 242-791-7
• Mol File: 19059-68-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 69 °C / 15mmHg
• Flash Point: 55.1°C
• Appearance: /
• Density: 0,86 g/cm3
• Refractive Index: 1.4320-1.4350
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 3-DIMETHYLAMINO-2,2-DIMETHYL-1-PROPANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 3-DIMETHYLAMINO-2,2-DIMETHYL-1-PROPANOL(19059-68-8)
• EPA Substance Registry System: 3-DIMETHYLAMINO-2,2-DIMETHYL-1-PROPANOL(19059-68-8)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• RIDADR: 2924
• HazardClass: 3/8
• PackingGroup: III
• Hazardous Substances Data: 19059-68-8(Hazardous Substances Data)

Usage

General Description

3-DIMETHYLAMINO-2,2-DIMETHYL-1-PROPANOL, also known as DMAEP or dimethylaminoethanol, is a chemical compound with a molecular formula C6H15NO. It is a tertiary amine and a colorless, viscous liquid that is commonly used as a pH adjuster, emulsifier, and conditioning agent in personal care products such as skin care, hair care, and cosmetics. DMAEP is known for its anti-aging properties and its ability to improve skin firmness, hydration, and texture. It is also used in the synthesis of pharmaceuticals and as a catalyst for the preparation of polyurethane foams. Despite its wide range of applications, DMAEP should be handled with caution as it is a skin and eye irritant and may cause respiratory irritation if inhaled.

Upstream product

• 15451-14-6 3-dimethylamino-2,2-dimethylpropanal 
• 114380-14-2 Trimethyl-<3-hydroxy-2.2-dimethyl-propyl>-ammoniumhydroxyd 
• 21678-37-5 N,N,2-trimethylpropionamide 
• 124-40-3 dimethyl amine 
• 40894-00-6 3-bromo-2,2-dimethyl-propan-1-ol 

Downstream Products

• 39943-25-4 4-nitro-benzoic acid-(3-dimethylamino-2,2-dimethyl-propyl ester) 
• 901308-39-2 C₃₇H₄₅F₃N₄O₄S 
• 870545-65-6 C₂₉H₃₇FN₄O₃ 
• 109469-13-8 4-butoxy-benzoic acid-(3-dimethylamino-2,2-dimethyl-propyl ester) 
• 114619-31-7 2,4-bis-(3-dimethylamino-2,2-dimethyl-propoxymethyl)-1-methoxy-benzene 
• 109469-21-8 4-isobutoxy-benzoic acid-(3-dimethylamino-2,2-dimethyl-propyl ester) 
• 39943-07-2 benzilic acid-(3-dimethylamino-2,2-dimethyl-propyl ester) 

Relevant articles and documents

METHOD FOR SYNTHESIZING AMINOALCOHOLS

The present invention relates to a method for synthesizing amonoalcohols (e.g., aminoalcohols that contain an amine group that is either unsubstituted, mono-substituted, or di-substituted) and to the products formed therefrom. In one embodiment, the present invention relates to a method for synthesizing aminoalcohols from a corresponding aminoaldehyde and to the products formed therefrom. In another embodiment, the present invention relates to a method for synthesizing aminoalcohols from a corresponding aminoaldehyde via a hydrogenation process using a suitable catalyst (e.g., Raney Nickel) and to the products formed therefrom. In still another embodiment, the present invention relates to aminoalcohols formed via direct hydrogenation from a corresponding aminoaldehyde without the intervening step of converting the aminoaldehyde starting material to a salt.

Investigation of the gem-Dialkyl effect in medicinal agents.

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