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31024-26-7

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31024-26-7 Usage

Description

(3-AMINOPROPYL)DIMETHYLMETHOXYSILANE, also known as 3-(Methoxydimethylsilyl)propylamine, is a clear colorless liquid that is a type of silane compound. It is known for its ability to functionalize surfaces, particularly aminosilanes, which makes it a valuable component in various applications across different industries.

Uses

Used in Scientific Research:
(3-AMINOPROPYL)DIMETHYLMETHOXYSILANE is used as a surface functionalization agent for aminosilanes mica in the field of atomic force microscopy. This application is crucial for enhancing the imaging capabilities of DNA, allowing for more detailed and accurate visualization of genetic material.
Used in Nanotechnology and Material Science:
In the nanotechnology and material science industries, (3-AMINOPROPYL)DIMETHYLMETHOXYSILANE is used as a coupling agent to improve the adhesion and compatibility between different materials. Its ability to bond with a variety of surfaces makes it an essential component in the development of advanced materials with specific properties.
Used in Coatings and Adhesives:
(3-AMINOPROPYL)DIMETHYLMETHOXYSILANE is used as a cross-linking agent in the formulation of coatings and adhesives. Its presence enhances the durability, water resistance, and overall performance of these products, making them more reliable for various applications.
Used in Electronics:
In the electronics industry, (3-AMINOPROPYL)DIMETHYLMETHOXYSILANE is used as a protective coating for sensitive components. Its ability to form a stable and uniform layer on surfaces helps to prevent damage from environmental factors, such as moisture and corrosive substances, thereby extending the lifespan of electronic devices.
Used in Biomedicine:
(3-AMINOPROPYL)DIMETHYLMETHOXYSILANE is used as a component in the development of biocompatible materials for medical applications. Its ability to bond with biological tissues and promote cell adhesion makes it a valuable asset in the creation of implants, prosthetics, and other medical devices.
Overall, (3-AMINOPROPYL)DIMETHYLMETHOXYSILANE is a versatile compound with a wide range of applications across various industries, thanks to its unique chemical properties and ability to functionalize surfaces.

Check Digit Verification of cas no

The CAS Registry Mumber 31024-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,0,2 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 31024-26:
(7*3)+(6*1)+(5*0)+(4*2)+(3*4)+(2*2)+(1*6)=57
57 % 10 = 7
So 31024-26-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H17NOSi/c1-8-9(2,3)6-4-5-7/h4-7H2,1-3H3

31024-26-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[methoxy(dimethyl)silyl]propan-1-amine

1.2 Other means of identification

Product number -
Other names 3-Aminopropyldimethylmethoxysilane

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:31024-26-7 SDS

31024-26-7Synthetic route

methanol
67-56-1

methanol

N-((3-aminopropyl)-dimethylsilyl)-2,2-dimethyl-1-aza-2-silacyclopentane
388606-32-4

N-((3-aminopropyl)-dimethylsilyl)-2,2-dimethyl-1-aza-2-silacyclopentane

(3-aminopropyl)dimethylmethoxysilane
31024-26-7

(3-aminopropyl)dimethylmethoxysilane

Conditions
ConditionsYield
In tetrahydrofuran at 0℃; under 750.075 Torr; Product distribution / selectivity;95%
methanol
67-56-1

methanol

(3-chloropropyl)dimethylchlorosilane
10605-40-0

(3-chloropropyl)dimethylchlorosilane

(3-aminopropyl)dimethylmethoxysilane
31024-26-7

(3-aminopropyl)dimethylmethoxysilane

Conditions
ConditionsYield
(i) NH3, (ii) /BRN= 1098229/; Multistep reaction;
methanol
67-56-1

methanol

N-((3-aminopropyl)-dimethylsilyl)-2,2-dimethyl-1-aza-2-silacyclopentane
388606-32-4

N-((3-aminopropyl)-dimethylsilyl)-2,2-dimethyl-1-aza-2-silacyclopentane

A

(3-aminopropyl)dimethylmethoxysilane
31024-26-7

(3-aminopropyl)dimethylmethoxysilane

B

di-3-(dimethylmethoxysilyl)propylamine
31024-66-5

di-3-(dimethylmethoxysilyl)propylamine

Conditions
ConditionsYield
In tetrahydrofuran at 20 - 40℃; under 750.075 Torr; for 3h; Product distribution / selectivity;
methanol
67-56-1

methanol

(3-chloropropyl)dimethylchlorosilane
10605-40-0

(3-chloropropyl)dimethylchlorosilane

A

(3-aminopropyl)dimethylmethoxysilane
31024-26-7

(3-aminopropyl)dimethylmethoxysilane

B

di-3-(dimethylmethoxysilyl)propylamine
31024-66-5

di-3-(dimethylmethoxysilyl)propylamine

Conditions
ConditionsYield
With ammonia at 133℃; under 40504.1 Torr; for 1.5h; Time; Temperature; Pressure; Autoclave; Overall yield = 79 %; Overall yield = 63 g;
(3-aminopropyl)dimethylmethoxysilane
31024-26-7

(3-aminopropyl)dimethylmethoxysilane

dihydroxy silicon(IV) phthalocyanine
19333-15-4

dihydroxy silicon(IV) phthalocyanine

C42H44N10O2Si3
886982-96-3

C42H44N10O2Si3

Conditions
ConditionsYield
With pyridine at 120℃;46%
(3-aminopropyl)dimethylmethoxysilane
31024-26-7

(3-aminopropyl)dimethylmethoxysilane

(2R,3R)-2,3-dibenzoyloxy-3-(butylcarbamoyl)propanoic acid
109976-14-9

(2R,3R)-2,3-dibenzoyloxy-3-(butylcarbamoyl)propanoic acid

(2R,3R)-2,3-Dibenzoyl-N-butyl-N'-<3-(dimethylmethoxysilyl)propyl>weinsaeure-diamid

(2R,3R)-2,3-Dibenzoyl-N-butyl-N'-<3-(dimethylmethoxysilyl)propyl>weinsaeure-diamid

Conditions
ConditionsYield
With dicyclohexyl-carbodiimide In tetrahydrofuran 1.) 0 deg. C, 2 h, 2.) room temperature, 12 h;
(3-aminopropyl)dimethylmethoxysilane
31024-26-7

(3-aminopropyl)dimethylmethoxysilane

N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide
82911-69-1

N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide

[3-(methoxy-dimethyl-silanyl)-propyl]-carbamic acid 9H-fluoren-9-ylmethyl ester

[3-(methoxy-dimethyl-silanyl)-propyl]-carbamic acid 9H-fluoren-9-ylmethyl ester

Conditions
ConditionsYield
In dichloromethane at 20℃; for 1h;
(3-aminopropyl)dimethylmethoxysilane
31024-26-7

(3-aminopropyl)dimethylmethoxysilane

N-succinimidyl-3-[3,3-dimethyl-6'-nitrospiro[2'H-chromene-2,2'-(2,3-dihydro-1H-indole)]-1-yl]-propionate
153711-72-9

N-succinimidyl-3-[3,3-dimethyl-6'-nitrospiro[2'H-chromene-2,2'-(2,3-dihydro-1H-indole)]-1-yl]-propionate

SP-APMS
1263362-66-8

SP-APMS

Conditions
ConditionsYield
In dichloromethane at 20℃; for 1h;
(3-aminopropyl)dimethylmethoxysilane
31024-26-7

(3-aminopropyl)dimethylmethoxysilane

n-hexadecanoyl chloride
112-67-4

n-hexadecanoyl chloride

N-[3-(dimethylmethoxysilyl)propyl]palmitamide
1240493-11-1

N-[3-(dimethylmethoxysilyl)propyl]palmitamide

Conditions
ConditionsYield
With triethylamine In toluene at 20℃; Inert atmosphere;
(3-aminopropyl)dimethylmethoxysilane
31024-26-7

(3-aminopropyl)dimethylmethoxysilane

C19H18Cl2N8O2

C19H18Cl2N8O2

C25H34ClN9O3Si

C25H34ClN9O3Si

Conditions
ConditionsYield
In tetrahydrofuran at 30℃; for 0.5h;0.362 g
(3-aminopropyl)dimethylmethoxysilane
31024-26-7

(3-aminopropyl)dimethylmethoxysilane

C19H16BrCl2N9O4

C19H16BrCl2N9O4

C25H32BrClN10O5Si

C25H32BrClN10O5Si

Conditions
ConditionsYield
In tetrahydrofuran at 30℃; for 0.5h;0.411 g
Dimethyl oxalate
553-90-2

Dimethyl oxalate

(3-aminopropyl)dimethylmethoxysilane
31024-26-7

(3-aminopropyl)dimethylmethoxysilane

C9H19NO4Si

C9H19NO4Si

Conditions
ConditionsYield
at 70 - 100℃; for 2.5h;192 g
(3-aminopropyl)dimethylmethoxysilane
31024-26-7

(3-aminopropyl)dimethylmethoxysilane

oxalic acid diethyl ester
95-92-1

oxalic acid diethyl ester

A

ethyl 2-((3-(methoxydimethylsilyl)propyl)amino)-2-oxoacetate

ethyl 2-((3-(methoxydimethylsilyl)propyl)amino)-2-oxoacetate

B

C11H23NO4Si

C11H23NO4Si

Conditions
ConditionsYield
at 22 - 70℃; for 3.5h; Overall yield = 412 g;

31024-26-7Downstream Products

31024-26-7Relevant articles and documents

METHOD FOR PREPARING AMINOPROPYLSILANES

-

Paragraph 0058-0062, (2021/09/17)

Aminopropylalkoxysilanes of the formula [in-line-formulae]H2N—CR2R3—CHR1—CH2—SiR4R5(OR6) ??I,[/in-line-formulae] are synthesized by hydrosilylating silazanes of the formulae and mixtures thereof, in the presence of a catalyst containing rhodium and/or iridium compounds, and then reacted with alcohol to form an aminopropylalkoxysilane.

PROCESS FOR PREPARING AMINOALKYLSILANES

-

Page/Page column 9-11, (2008/06/13)

The invention relates to a process for preparing aminoalkylsilanes.

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