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3405-42-3

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3405-42-3 Usage

General Description

N-Methyldipropylamine is a chemical compound with the molecular formula C8H19N. It is an organic compound that belongs to the class of amines and is commonly used as an intermediate in the production of various chemicals. N-Methyldipropylamine is a clear, colorless liquid with a faint amine-like odor and is highly soluble in water. It is primarily utilized as a catalyst in the production of polyurethane and as an intermediate in the synthesis of pharmaceuticals, agricultural chemicals, and other organic compounds. This chemical is known to have low acute toxicity, but proper handling and safety measures should still be followed due to its potential to cause irritation to the skin, eyes, and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 3405-42-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,0 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3405-42:
(6*3)+(5*4)+(4*0)+(3*5)+(2*4)+(1*2)=63
63 % 10 = 3
So 3405-42-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H17N/c1-4-6-8(3)7-5-2/h4-7H2,1-3H3

3405-42-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-N-propylpropan-1-amine

1.2 Other means of identification

Product number -
Other names Methyl-dipropyl-amin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3405-42-3 SDS

3405-42-3Synthetic route

(5-fluoroindol-3-yl)dimethylsulfonium perchlorate
1440957-24-3

(5-fluoroindol-3-yl)dimethylsulfonium perchlorate

di-n-propylamine
142-84-7

di-n-propylamine

A

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

B

5-fluoro-(3-thiomethyl)-indole

5-fluoro-(3-thiomethyl)-indole

Conditions
ConditionsYield
for 1h; Inert atmosphere; Reflux;A n/a
B 98.5%
di-n-propylamine
142-84-7

di-n-propylamine

(1H-indol-3-yl)dimethylsulfonium perchlorate

(1H-indol-3-yl)dimethylsulfonium perchlorate

A

3-methylthioindole
40015-10-9

3-methylthioindole

B

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

Conditions
ConditionsYield
at 107℃; for 1h; Inert atmosphere;A 98.1%
B n/a
(5-methylindol-3-yl)dimethylsulfonium perchlorate
1440957-18-5

(5-methylindol-3-yl)dimethylsulfonium perchlorate

di-n-propylamine
142-84-7

di-n-propylamine

A

5-methyl-3-(methylthio)-1H-indole
40015-14-3

5-methyl-3-(methylthio)-1H-indole

B

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

Conditions
ConditionsYield
for 1h; Inert atmosphere; Reflux;A 96.6%
B n/a
(2-methylthioindol-3-yl)dimethylsulfonium perchlorate
1440957-15-2

(2-methylthioindol-3-yl)dimethylsulfonium perchlorate

di-n-propylamine
142-84-7

di-n-propylamine

A

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

B

2,3-bis(methylthio)indole
120517-33-1

2,3-bis(methylthio)indole

Conditions
ConditionsYield
for 1h; Inert atmosphere; Reflux;A n/a
B 96.5%
(5-nitroindol-3-yl)dimethylsulfonium perchlorate
1440957-22-1

(5-nitroindol-3-yl)dimethylsulfonium perchlorate

di-n-propylamine
142-84-7

di-n-propylamine

A

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

B

3-methylthio-5-nitroindole
1416438-63-5

3-methylthio-5-nitroindole

Conditions
ConditionsYield
for 1h; Inert atmosphere; Reflux;A n/a
B 94.4%
(4-bromoindol-3-yl)dimethylsulfonium perchlorate
1440957-28-7

(4-bromoindol-3-yl)dimethylsulfonium perchlorate

di-n-propylamine
142-84-7

di-n-propylamine

A

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

B

4-bromo-3-methylthioindole
1401844-08-3

4-bromo-3-methylthioindole

Conditions
ConditionsYield
for 1h; Inert atmosphere; Reflux;A n/a
B 93.1%
formaldehyd
50-00-0

formaldehyd

di-n-propylamine
142-84-7

di-n-propylamine

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

Conditions
ConditionsYield
With zinc(II) tetrahydroborate; zinc(II) chloride In tetrahydrofuran for 8h; Ambient temperature;92%
With formic acid
With formic acid Eschweiler-Clarke reaction; Reflux;
With potassium hydroxide In water at 80℃; for 2h; Time; Temperature;
(indol-3-yl)methylphenylsulfonium perchlorate
1440957-32-3

(indol-3-yl)methylphenylsulfonium perchlorate

di-n-propylamine
142-84-7

di-n-propylamine

A

3-phenylthioindole
54491-43-9

3-phenylthioindole

B

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

Conditions
ConditionsYield
for 1h; Inert atmosphere; Reflux;A 90.1%
B n/a
bis(indol-3-yl)methylsulfonium perchlorate

bis(indol-3-yl)methylsulfonium perchlorate

di-n-propylamine
142-84-7

di-n-propylamine

A

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

B

3,3'-bis(indolyl) sulfide
1484-18-0

3,3'-bis(indolyl) sulfide

Conditions
ConditionsYield
for 1h; Inert atmosphere; Reflux;A n/a
B 87.3%
(5-cyanoindol-3-yl)dimethylsulfonium perchlorate
1440957-20-9

(5-cyanoindol-3-yl)dimethylsulfonium perchlorate

di-n-propylamine
142-84-7

di-n-propylamine

A

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

B

3-methylthioindole-5-carbonitrile
1416438-98-6

3-methylthioindole-5-carbonitrile

Conditions
ConditionsYield
for 1h; Inert atmosphere; Reflux;A n/a
B 84.6%
(5-bromoindol-3-yl)dimethylsulfonium perchlorate
1440957-26-5

(5-bromoindol-3-yl)dimethylsulfonium perchlorate

di-n-propylamine
142-84-7

di-n-propylamine

A

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

B

5-bromo-3-(methylthio)-1H-indole

5-bromo-3-(methylthio)-1H-indole

Conditions
ConditionsYield
for 1h; Inert atmosphere; Reflux;A n/a
B 84.5%
(2-carboethoxyindol-3-yl)dimethylsulfonium perchlorate
1440957-30-1

(2-carboethoxyindol-3-yl)dimethylsulfonium perchlorate

di-n-propylamine
142-84-7

di-n-propylamine

A

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

B

ethyl 3-methylthio-1H-indole-2-carboxylate
154422-23-8

ethyl 3-methylthio-1H-indole-2-carboxylate

Conditions
ConditionsYield
for 1h; Inert atmosphere; Reflux;A n/a
B 81.9%
(5-methoxyindol-3-yl)dimethylsulfonium perchlorate
1440957-17-4

(5-methoxyindol-3-yl)dimethylsulfonium perchlorate

di-n-propylamine
142-84-7

di-n-propylamine

A

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

B

5-methoxy-3-methylthioindole
1416438-06-6

5-methoxy-3-methylthioindole

Conditions
ConditionsYield
for 1h; Inert atmosphere; Reflux;A n/a
B 81.7%
(3-methylthio-5-nitroindol-2-yl)dimethylsulfonium perchlorate

(3-methylthio-5-nitroindol-2-yl)dimethylsulfonium perchlorate

di-n-propylamine
142-84-7

di-n-propylamine

A

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

B

2,3-bis(methylthio)-5-nitroindole
1440957-35-6

2,3-bis(methylthio)-5-nitroindole

Conditions
ConditionsYield
for 2h; Inert atmosphere; Reflux;A n/a
B 76.9%
ethylmagnesium bromide
925-90-6

ethylmagnesium bromide

3-methyl-1,5,3-dioxazepane
86967-43-3

3-methyl-1,5,3-dioxazepane

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

Conditions
ConditionsYield
35%
potassium methyl sulfate
562-54-9

potassium methyl sulfate

di-n-propylamine
142-84-7

di-n-propylamine

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

Conditions
ConditionsYield
With water
di-n-propylamine
142-84-7

di-n-propylamine

methyl iodide
74-88-4

methyl iodide

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

nitromethane
75-52-5

nitromethane

propionaldehyde
123-38-6

propionaldehyde

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

Conditions
ConditionsYield
With ethanol; acetic acid; platinum Hydrogenation;
Methyltrimethoxyphosphonium tetrafluoroborate
15294-11-8

Methyltrimethoxyphosphonium tetrafluoroborate

di-n-propylamine
142-84-7

di-n-propylamine

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

Conditions
ConditionsYield
for 12h; Ambient temperature;51 % Chromat.
nitromethane
75-52-5

nitromethane

ethanol
64-17-5

ethanol

acetic acid
64-19-7

acetic acid

propionaldehyde
123-38-6

propionaldehyde

hydrogen

hydrogen

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

Conditions
ConditionsYield
in Gegenwart von Platinoxyd; analoge Reaktion mit Nitrobenzol;
ethene
74-85-1

ethene

dimethyl amine
124-40-3

dimethyl amine

CO

CO

iron pentacarbonyl

iron pentacarbonyl

water

water

A

formic acid
64-18-6

formic acid

B

N,N-dimethylaminopropane
926-63-6

N,N-dimethylaminopropane

C

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

Conditions
ConditionsYield
at 120 - 125℃; under 139746 - 147102 Torr;
at 120 - 125℃; under 139746 - 147102 Torr;
ethene
74-85-1

ethene

water
7732-18-5

water

methylamine
74-89-5

methylamine

CO

CO

Fe(CO)5

Fe(CO)5

A

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

B

methyl-n-propylamine
627-35-0

methyl-n-propylamine

Conditions
ConditionsYield
at 120 - 140℃; under 125036 - 132391 Torr;
at 120 - 140℃; under 125036 - 132391 Torr;
ethene
74-85-1

ethene

dimethyl amine
124-40-3

dimethyl amine

CO

CO

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

Conditions
ConditionsYield
With iron pentacarbonyl; water at 120 - 140℃; under 125036 - 147102 Torr;
With iron pentacarbonyl; water at 120 - 140℃; under 125036 - 147102 Torr;
ethene
74-85-1

ethene

methylamine
74-89-5

methylamine

CO

CO

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

Conditions
ConditionsYield
With iron pentacarbonyl; water at 120 - 140℃; under 125036 - 147102 Torr;
With iron pentacarbonyl; water at 120 - 140℃; under 125036 - 147102 Torr;
dimethylamine formate

dimethylamine formate

pentacarbonyl iron

pentacarbonyl iron

A

N,N-dimethylaminopropane
926-63-6

N,N-dimethylaminopropane

B

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

Conditions
ConditionsYield
With ethene; carbon monoxide at 130℃; under 147102 Torr;
ammonia
7664-41-7

ammonia

tri-n-propyl-methylammonium chloride
75373-66-9

tri-n-propyl-methylammonium chloride

potassium

potassium

A

tri-n-propylamine
102-69-2

tri-n-propylamine

B

propene
187737-37-7

propene

C

methane
34557-54-5

methane

D

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

Conditions
ConditionsYield
at -78℃; Mechanism;
tri-n-propyl-methylammonium iodide
3531-14-4

tri-n-propyl-methylammonium iodide

ammonia
7664-41-7

ammonia

sodium

sodium

A

tri-n-propylamine
102-69-2

tri-n-propylamine

B

propene
187737-37-7

propene

C

methane
34557-54-5

methane

D

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

Conditions
ConditionsYield
at -33℃; Mechanism;
N,N-di-n-propylformamide
6282-00-4

N,N-di-n-propylformamide

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

Conditions
ConditionsYield
With hydrogen In 1,2-dimethoxyethane at 160℃; under 22502.3 Torr; for 20h; Inert atmosphere; Autoclave; Molecular sieve;
methanol
67-56-1

methanol

di-n-propylamine
142-84-7

di-n-propylamine

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

Conditions
ConditionsYield
With Iridium(II)-coordinated mesoporous (4-[5-(4-aminophenyl)-4'-methyl-[1,1'-biphenyl]-3-yl]aniline)-modified Tröger’s base-functionalized polymer at 110℃; for 24h;60 %Chromat.
With potassium phosphate; tris(2-diphenylphosphinoethyl)phosphine; cobalt acetylacetonate at 140℃; for 24h; Inert atmosphere; Autoclave;> 99 %Chromat.
N-methyldipropylamine
3405-42-3

N-methyldipropylamine

24-nor-23-iodo-3α,12α-dihydroxy-7-deoxy-5β-cholane
141417-62-1

24-nor-23-iodo-3α,12α-dihydroxy-7-deoxy-5β-cholane

N-(3α,12α-dihydroxy-24-nor-5β-cholan-23-yl) N-methyl-N,N-dipropylammonium iodide

N-(3α,12α-dihydroxy-24-nor-5β-cholan-23-yl) N-methyl-N,N-dipropylammonium iodide

Conditions
ConditionsYield
In acetonitrile for 6h; Heating;75%
N-methyldipropylamine
3405-42-3

N-methyldipropylamine

hexadecanyl bromide
112-82-3

hexadecanyl bromide

N-hexadecyl-N-methyl-N,N-dipropylammonium bromide

N-hexadecyl-N-methyl-N,N-dipropylammonium bromide

Conditions
ConditionsYield
In acetonitrile for 12h; Reflux;74%
N-methyldipropylamine
3405-42-3

N-methyldipropylamine

2-bromoethanol
540-51-2

2-bromoethanol

N-(2-hydroxyethyl)-N-methyl-N-propylpropan-1-ammoniumbromide
1206209-08-6

N-(2-hydroxyethyl)-N-methyl-N-propylpropan-1-ammoniumbromide

Conditions
ConditionsYield
In acetonitrile for 4h; Reflux;68%
5-methyl-1,3-benzoxazole
10531-78-9

5-methyl-1,3-benzoxazole

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

5-methyl-N,N-dipropylbenzo[d]oxazol-2-amine
1373348-99-2

5-methyl-N,N-dipropylbenzo[d]oxazol-2-amine

Conditions
ConditionsYield
With tert.-butylhydroperoxide; tetra-(n-butyl)ammonium iodide; acetic acid In water; acetonitrile at 100℃; for 0.333333h; Microwave irradiation; Green chemistry;57%
benzoxazole
273-53-0

benzoxazole

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

N,N-dipropylbenzo[d]oxazol-2-amine
1262296-99-0

N,N-dipropylbenzo[d]oxazol-2-amine

Conditions
ConditionsYield
With tert.-butylhydroperoxide; tetra-(n-butyl)ammonium iodide; acetic acid In water; acetonitrile at 100℃; for 0.333333h; Microwave irradiation; Green chemistry;55%
4-toluenesulfonyl azide
941-55-9

4-toluenesulfonyl azide

N-methyldipropylamine
3405-42-3

N-methyldipropylamine

(E)-N'-((4-methylphenyl)sulfonyl)-N,N-dipropylformimidamide
1204768-66-0

(E)-N'-((4-methylphenyl)sulfonyl)-N,N-dipropylformimidamide

Conditions
ConditionsYield
With 4-nitroacenaphthene In dichloromethane at 20℃; for 12h; Irradiation;32%
N-methyldipropylamine
3405-42-3

N-methyldipropylamine

methyl iodide
74-88-4

methyl iodide

dimethyl-dipropyl-ammonium; iodide

dimethyl-dipropyl-ammonium; iodide

Conditions
ConditionsYield
With diethyl ether
N-methyldipropylamine
3405-42-3

N-methyldipropylamine

1-Chloro-1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoro-6-iodo-hexane
16486-97-8

1-Chloro-1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoro-6-iodo-hexane

A

1-chloro-1H,6H-dodecafluoro-hexane
307-22-2

1-chloro-1H,6H-dodecafluoro-hexane

B

<2-methyl-2-(ω-chlorododecafluoro-n-hexyl)vinyl>-n-propylmethylamine
108836-08-4

<2-methyl-2-(ω-chlorododecafluoro-n-hexyl)vinyl>-n-propylmethylamine

Conditions
ConditionsYield
With tetrakis(triphenylphosphine) palladium(0) In hexane at 60℃; for 0.5h;

3405-42-3Downstream Products

3405-42-3Relevant articles and documents

Simplified preparation of a graphene-co-shelled Ni/NiO@C nano-catalyst and its application in theN-dimethylation synthesis of amines under mild conditions

Liu, Jianguo,Ma, Longlong,Song, Yanpei,Zhang, Mingyue,Zhuang, Xiuzheng

supporting information, p. 4604 - 4617 (2021/06/30)

The development of Earth-abundant, reusable and non-toxic heterogeneous catalysts to be applied in the pharmaceutical industry for bio-active relevant compound synthesis remains an important goal of general chemical research.N-methylated compounds, as one of the most essential bioactive compounds, have been widely used in the fine and bulk chemical industries for the production of high-value chemicals. Herein, an environmentally friendly and simplified method for the preparation of graphene encapsulated Ni/NiO nanoalloy catalysts (Ni/NiO@C) was developed for the first time, for the highly selective synthesis ofN-methylated compounds using various functional amines and aldehydes under easy to handle, and industrially applicable conditions. A large number of primary and secondary amines (more than 70 examples) could be converted to the correspondingN,N-dimethylamines with the participation of different functional aldehydes, with an average yield of over 95%. A gram-scale synthesis also demonstrated a similar yield when compared with the benchmark test. In addition, it was further proved that the catalyst could easily be recycled because of its intrinsic magnetism and reused up to 10 times without losing its activity and selectivity. Also, for the first time, the tandem synthesis ofN,N-dimethylamine products in a one-pot process, using only a single earth-abundant metal catalyst, whose activity and selectivity were more than 99% and 94%, respectively, for all tested substrates, was developed. Overall, the advantages of this newly developed method include operational simplicity, high stability, easy recyclability, cost-effectiveness of the catalyst, and good functional group compatibility for the synthesis ofN-methylation products as well as the industrially applicable tandem synthesis process.

Efficient Cobalt-Catalyzed Methylation of Amines Using Methanol

Liu, Zhenghui,Yang, Zhenzhen,Yu, Xiaoxiao,Zhang, Hongye,Yu, Bo,Zhao, Yanfei,Liu, Zhimin

supporting information, p. 4278 - 4283 (2017/10/23)

The methylation of amines using methanol is a promising route to synthesize N-methylamines, and the development of cheap and efficient catalytic system for this reaction is of great significance. Herein, we reported a cobalt (Co)-based catalytic system, which was in situ formed from commercially available Co precursor and a tetradentate phosphine ligand P(CH2CH2PPh2)3 combined with K3PO4. This catalystic system was very effective for the selective production of dimethylated products from aliphatic amines and monomethylated ones from aromatic amines. The reaction mechanism was further investigated by control and isotope labelling experiments. (Figure presented.).

Catalytic hydrogenation of amides to amines under mild conditions

Stein, Mario,Breit, Bernhard

supporting information, p. 2231 - 2234 (2013/03/28)

Under (not so much) pressure: A general method for the hydrogenation of tertiary and secondary amides to amines with excellent selectivity using a bimetallic Pd-Re catalyst has been developed. The reaction proceeds under low pressure and comparatively low temperature. This method provides organic chemists with a simple and reliable tool for the synthesis of amines. Copyright

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