dimethyl amine
methyloxirane
1-methyl-2-N,N-dimethylaminoethanol
Conditions | Yield |
---|---|
With diisopropanolamine at 70℃; under 5250.53 Torr; for 3h; Reagent/catalyst; Pressure; Temperature; | 99.6% |
With methanol at 60℃; | |
In ethanol Heating; |
formaldehyd
3-amino-2-propanol
1-methyl-2-N,N-dimethylaminoethanol
Conditions | Yield |
---|---|
With formic acid for 24h; Heating; | 60% |
tetramethyldiamidothiophosphoric acid
methyloxirane
A
1-methyl-2-N,N-dimethylaminoethanol
B
tetramethylphosphorodiamidous acid
C
2-oxo-2-dimethylamino-4-methyl-1,3,2-thiaoxaphospholane
Conditions | Yield |
---|---|
In 1,4-dioxane at 100 - 110℃; for 4h; | A n/a B n/a C 20% |
1,1-dimethyl-1-(2-hydroxypropyl)amine benzoylformimide
A
1-methyl-2-N,N-dimethylaminoethanol
B
2,3-dihydroxy-2,3-diphenyl-succinic acid diamide
Conditions | Yield |
---|---|
In methanol at 20 - 30℃; for 0.833333h; UV-irradiation; | A n/a B 10% |
Conditions | Yield |
---|---|
With benzene at 125℃; |
Conditions | Yield |
---|---|
With sodium hydroxide at 40℃; | |
With toluene at 95 - 100℃; | |
at 100℃; | |
With sodium hydroxide at 40℃; |
formaldehyd
formic acid
3-amino-2-propanol
1-methyl-2-N,N-dimethylaminoethanol
Conditions | Yield |
---|---|
With water |
dimethylaminoacetone
1-methyl-2-N,N-dimethylaminoethanol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether | |
(reduction); |
C13H18(125)INO3
A
1-methyl-2-N,N-dimethylaminoethanol
Conditions | Yield |
---|---|
With phosphate buffer at 37℃; for 0.0833333h; chemical stability to hydrolysis; var.: time; |
dimethylaminoacetone
1-methyl-2-N,N-dimethylaminoethanol
Conditions | Yield |
---|---|
With nitrogen In methanol; dichloromethane |
1,1-dimethyl-1-(2-hydroxypropyl)amine benzoylformimide
A
1-methyl-2-N,N-dimethylaminoethanol
B
benzoyl isocyanate
Conditions | Yield |
---|---|
Kinetics; Temperature; Solvent; Curtius rearrangement; Pyrolysis; |
D-glucose
dimethyl amine
A
2-(N,N-dimethylamino)ethanol
B
1-methyl-2-N,N-dimethylaminoethanol
C
N,N,N,N,-tetramethylethylenediamine
D
1,2-bis(dimethylamino)propane
E
dimethylaminoacetone
F
N,N-dimethyl-formamide
Conditions | Yield |
---|---|
With 5 wt% ruthenium/carbon; hydrogen In water at 124.84℃; under 37503.8 Torr; for 1h; Catalytic behavior; Pressure; Temperature; |
D-glucose
dimethyl amine
A
2-(N,N-dimethylamino)ethanol
B
1-methyl-2-N,N-dimethylaminoethanol
C
N,N,N,N,-tetramethylethylenediamine
D
1,2-bis(dimethylamino)propane
E
N,N-dimethyl-formamide
Conditions | Yield |
---|---|
With 5 wt% ruthenium/carbon; hydrogen In water at 124.84℃; under 37503.8 Torr; for 1h; |
D-glucose
dimethyl amine
A
2-(N,N-dimethylamino)ethanol
B
1-methyl-2-N,N-dimethylaminoethanol
C
N,N,N,N,-tetramethylethylenediamine
D
1,2-bis(dimethylamino)propane
E
dimethylaminoacetone
Conditions | Yield |
---|---|
With 5 wt% ruthenium/carbon; hydrogen In water at 124.84℃; under 56255.6 Torr; for 1h; |
D-fructose
dimethyl amine
A
2-(N,N-dimethylamino)ethanol
B
1-methyl-2-N,N-dimethylaminoethanol
C
N,N,N,N,-tetramethylethylenediamine
D
1,2-bis(dimethylamino)propane
E
dimethylaminoacetone
Conditions | Yield |
---|---|
With 5 wt% ruthenium/carbon; hydrogen In water at 124.84℃; under 56255.6 Torr; for 1h; |
1-methyl-2-N,N-dimethylaminoethanol
copper(II) methoxide
Cu(OCH(CH3)CH2N(CH3)2)2
Conditions | Yield |
---|---|
(Ar); room temp.; | 100% |
In not given prepd. by the alcohol-exchange procedure described by Singh, J. V.; Baranwal, B. P.; Mehrotra, R. C.; T. Anorg. Allg. Chem. 1981, 477, 235; sublimation, crystn. from hexane; | 75% |
Conditions | Yield |
---|---|
In toluene N2-atmosphere; refluxing; evapn.; elem. anal.; | 100% |
1-methyl-2-N,N-dimethylaminoethanol
Conditions | Yield |
---|---|
In hexane byproducts: HN(Si(CH3)3)2; under dry N2; alcohol added to soln. of Zn-compd., exothermic reaction, refluxed for 2h,; volatiles removed in vac., distn. (170°C bath, 10**-4 Torr; elem. anal.; | 97% |
Conditions | Yield |
---|---|
With thionyl chloride In chloroform at 0 - 20℃; for 1h; Reflux; | 95% |
With thionyl chloride In chloroform | 95% |
With thionyl chloride In chloroform Reflux; Cooling with ice; |
1-methyl-2-N,N-dimethylaminoethanol
triethyl gallium
[(C2H5)2Ga(OCH(CH3)CH2N(CH3)2)]2
Conditions | Yield |
---|---|
In dichloromethane (N2); using Schlenk techniques; addn. dropwise of HOCH(CH3)CH2NMe2 (1 equiv.) to soln. of Et3Ga (1 equiv.) in CH2Cl2 at -78°C with stirring for 0.5 h; slow warming to room temp., stirring for 5 h; removal of solvent in vac., redissolving in toluene and cooling to -20°C; as solid; elem. anal.; | 95% |
In hexane (N2); using Schlenk techniques; treatment of HOCH(CH3)CH2NMe2 (1 equiv.)with Et3Ga (1 equiv.) in hexane at room temp.; |
1-methyl-2-N,N-dimethylaminoethanol
bis(bis(trimethylsilyl)amido)tin(II)
Conditions | Yield |
---|---|
With trimethyl orthoformate In hexane at 20℃; for 19h; Cooling with ice; | 95% |
1-methyl-2-N,N-dimethylaminoethanol
triethyl gallium
((C2H5)2Ga(OCH(CH3)CH2N(CH3)2))2
Conditions | Yield |
---|---|
In toluene byproducts: ethane; under N2; ligand added dropwise to soln. of Et3Ga (molar ratio 1:1) in toluene at -78°C with stirring over 0.5 h; warmed slowly to room temp.; stirred for 24 h; solvent removed in vac.; crystd. by standing at room temp. for several d; elem. anal.; | 92% |
Conditions | Yield |
---|---|
In propan-1-ol at 85℃; for 18.5h; | 91% |
Conditions | Yield |
---|---|
In pentane at 20℃; for 1h; Schlenk technique; Inert atmosphere; | 91% |
lithium aluminium tetrahydride
1-methyl-2-N,N-dimethylaminoethanol
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: H2; all manipulations under N2; soln. of org. compd. added to stirred soln. of LiAlH4 in ratio of 2:1 at -25°C, stirred for 1 h at ambient temp.; pentane added, crystd. at -20°C, filtered, solvents removed from filtrate, oily product crystd. by washing with pentane; elem. anal.; | 90.4% |
1-methyl-2-N,N-dimethylaminoethanol
[1,3,2]dioxaphospholan-2-yl-dimethyl-amine
2-<(2-dimethylamino-1-methyl)ethoxy>-1,3,2-dioxaphospholane
Conditions | Yield |
---|---|
at 130℃; for 0.0833333h; | 87% |
1-methyl-2-N,N-dimethylaminoethanol
octyl chloromethyl ether
Conditions | Yield |
---|---|
In hexane at 20℃; Menschutkin's reaction; | 87% |
In hexane for 0.166667h; Menschutkin reaction; |
1-methyl-2-N,N-dimethylaminoethanol
1-chloromethoxy-decane
Conditions | Yield |
---|---|
In hexane at 20℃; Menschutkin's reaction; | 87% |
In hexane for 0.166667h; Menschutkin reaction; |
1-methyl-2-N,N-dimethylaminoethanol
1-chloromethoxy-nonane
Conditions | Yield |
---|---|
In hexane at 20℃; Menschutkin's reaction; | 86% |
In hexane for 0.166667h; Menschutkin reaction; |
Conditions | Yield |
---|---|
In hexane at 20℃; Menschutkin's reaction; | 86% |
1-methyl-2-N,N-dimethylaminoethanol
Conditions | Yield |
---|---|
With Na In toluene byproducts: NaCl; N2-atmosphere; 80°C (2 h), Ni-complex addn., refluxing (2 h); decanting, crystn. on concg. (-15°C, overnight), filtering, washing (hexane), drying; elem. anal.; | 86% |
1-methyl-2-N,N-dimethylaminoethanol
zinc(II) chloride
[Chloro-(rac-1-dimethylaminoisopropanolato)-zink(II)]4
Conditions | Yield |
---|---|
In methanol rac-1-dimethylaminoisopropanol slowly added dropwise to ZnCl2 soln. in MeOH under stirring; stirred for 2 days; heated for 2 h under reflux; cooled slowly to -5°C; left standing for 3 days; washed with n-haxane; recrystallized from MeOH; dried in vacuum; elem. anal.; | 86% |
1-methyl-2-N,N-dimethylaminoethanol
1-chloromethoxy-pentane
Conditions | Yield |
---|---|
In hexane at 20℃; Menschutkin's reaction; | 85% |
1-methyl-2-N,N-dimethylaminoethanol
octadecyl chloromethyl ether
Conditions | Yield |
---|---|
In hexane at 20℃; Menschutkin's reaction; | 85% |
In hexane for 0.166667h; Menschutkin reaction; |
1-methyl-2-N,N-dimethylaminoethanol
1-(chloromethoxy)tetradecane
Conditions | Yield |
---|---|
In hexane at 20℃; Menschutkin's reaction; | 85% |
In hexane for 0.166667h; Menschutkin reaction; |
1-methyl-2-N,N-dimethylaminoethanol
tributyltin ethoxide
(C4H9)3SnOCH(CH3)CH2N(CH3)2
Conditions | Yield |
---|---|
In benzene byproducts: C2H5OH; 1:1; azeotropic removal of C2H5OH; | 85% |
byproducts: C2H5OH; equimolar amts. of educts, heated; remove alc.; | 85% |
byproducts: C2H5OH; equimolar amts. of educts, heated; remove alc.; | 85% |
In benzene byproducts: C2H5OH; 1:1; azeotropic removal of C2H5OH; | 85% |
1-methyl-2-N,N-dimethylaminoethanol
tributyltin methoxide
(C4H9)3SnOCH(CH3)CH2N(CH3)2
Conditions | Yield |
---|---|
byproducts: CH3OH; equimolar amts. of educts, heated; remove alc.; | 85% |
byproducts: CH3OH; equimolar amts. of educts, heated; remove alc.; | 85% |
1-methyl-2-N,N-dimethylaminoethanol
hexyloxymethyl chloride
Conditions | Yield |
---|---|
In hexane at 20℃; Menschutkin's reaction; | 84% |
In hexane for 0.166667h; Menschutkin reaction; | 83.5% |
1-methyl-2-N,N-dimethylaminoethanol
1-chloromethoxy-hexadecane
Conditions | Yield |
---|---|
In hexane at 20℃; Menschutkin's reaction; | 84% |
In hexane for 0.166667h; Menschutkin reaction; |
1-methyl-2-N,N-dimethylaminoethanol
chloromethyl undecyl ether
Conditions | Yield |
---|---|
In hexane at 20℃; Menschutkin's reaction; | 84% |
In hexane for 0.166667h; Menschutkin reaction; |
Conditions | Yield |
---|---|
With dmap; triethylamine In dichloromethane at 20℃; for 24h; | 84% |
With dmap; triethanolamine In dichloromethane at 20℃; Inert atmosphere; Cooling with ice; |
1-methyl-2-N,N-dimethylaminoethanol
pyrocatechol phosphorochloridite
1-methyl-2-(dimethylamino)ethyl o-phenylene phosphite
Conditions | Yield |
---|---|
With triethylamine In benzene Heating; | 83% |
Conditions | Yield |
---|---|
In hexane at 20℃; Menschutkin's reaction; | 83% |
IUPAC Name: 1-Dimethylamino-2-propanol
The MF of 1-Dimethylamino-2-propanol (108-16-7) is C5H13NO.
The MW of 1-Dimethylamino-2-propanol (108-16-7) is 103.16.
Synonyms of 1-Dimethylamino-2-propanol (108-16-7): 1-(Dimethylamino)-2-propano ; 1,1-Dimethylaminopropan-2-ol ; 1-Dimethylaminopropan-2-ol ; 1-N,N-Dimethylin-2-propanolamine ; 2-Propanol,1,1-(dimethylamino)- ; Dimethyl(2-hydroxypropyl)amine
Stability: Stable. Flammable. Incompatible with strong oxidizing agents, amines, acids
Form: light yellow liquid
Index of Refraction: 1.436
EINECS: 203-556-4
Density: 0.887 g/ml
Flash Point: 25.6 °C
Boiling Point: 124 °C
Melting Point: -85 °C
Storage temp: Flammables area
Water Solubility: miscible
1-Dimethylamino-2-propanol (108-16-7) is used for the pharmaceutical industry, also used as a stabilizer of acrylonitrile polymer.
Hydrochloric acid---Sodium hydroxide---Diethyl ether---Formaldehyde---Formic acid---Amino-2-propanol
1. | skn-rbt 10 mg/24H MLD | AMIHBC AMA Archives of Industrial Hygiene and Occupational Medicine. 10 (1954),61. | ||
2. | skn-rbt 500 mg MOD | FCTOD7 Food and Chemical Toxicology. 20 (1982),563. | ||
3. | eye-rbt 250 µg SEV | AMIHBC AMA Archives of Industrial Hygiene and Occupational Medicine. 10 (1954),61. | ||
4. | eye-rbt 100 mg/4S rns SEV | FCTOD7 Food and Chemical Toxicology. 20 (1982),573. | ||
5. | orl-rat LD50:1890 mg/kg | AMIHBC AMA Archives of Industrial Hygiene and Occupational Medicine. 10 (1954),61. |
Reported in EPA TSCA Inventory.
Moderately toxic by ingestion. A skin and severe eye irritant. Used in boiler water condensate corrosion control. Dangerous fire hazard when exposed to heat or flame. Can react vigorously with oxidizers. To fight fire, use foam, CO2, dry chemical. When heated to decomposition it emits toxic fumes of NOx. See also AMINES.Safety information of 1-Dimethylamino-2-propanol (108-16-7):
Hazard Codes C
Risk Statements
10 Flammable
22 Harmful if swallowed
34 Causes burns
Safety Statements
26 In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
36/37/39 Wear suitable protective clothing, gloves and eye/face protection
45 In case of accident or if you feel unwell, seek medical advice immediately (show label where possible)
23 Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer)
RIDADR UN 2734 8/PG 2
WGK Germany 1
RTECS UB3150000
F 10-34
HazardClass 8
PackingGroup II
HS Code 29221980
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