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4253-76-3

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4253-76-3 Usage

General Description

N-octadecylpropane-1,3-diamine, also known as octadecylamine, is a chemical compound with the molecular formula C21H49N. It is an organic compound that belongs to the class of amines, containing a long hydrocarbon chain attached to a central amine group. Octadecylamine is commonly used as a surfactant, emulsifier, and corrosion inhibitor in various industrial applications. It is also used as a raw material for the synthesis of other chemicals and as a component in the production of detergents, paper products, and textiles. Additionally, it has antimicrobial properties and is sometimes utilized in the preservation of wood and other materials. However, it is important to handle octadecylamine with care, as it can cause irritation to the skin, eyes, and respiratory tract.

Check Digit Verification of cas no

The CAS Registry Mumber 4253-76-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,5 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4253-76:
(6*4)+(5*2)+(4*5)+(3*3)+(2*7)+(1*6)=83
83 % 10 = 3
So 4253-76-3 is a valid CAS Registry Number.
InChI:InChI=1/C21H46N2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20-23-21-18-19-22/h23H,2-22H2,1H3

4253-76-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-octadecylpropane-1,3-diamine

1.2 Other means of identification

Product number -
Other names N-octadecyl-propanediyldiamine

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:4253-76-3 SDS

4253-76-3Synthetic route

N-Boc-N’-stearoyl-1,3-diamine

N-Boc-N’-stearoyl-1,3-diamine

N-octadecyl-propane-1,3-diamine
4253-76-3

N-octadecyl-propane-1,3-diamine

Conditions
ConditionsYield
With trifluoroacetic acid In dichloromethane for 1h;100%
N-octadecyl-β-alanine nitrile
6281-72-7

N-octadecyl-β-alanine nitrile

N-octadecyl-propane-1,3-diamine
4253-76-3

N-octadecyl-propane-1,3-diamine

Conditions
ConditionsYield
With ethanol; nickel at 95℃; under 14710.2 Torr; Hydrogenation;
β-alanine N-octadecylamide
56426-61-0

β-alanine N-octadecylamide

N-octadecyl-propane-1,3-diamine
4253-76-3

N-octadecyl-propane-1,3-diamine

Conditions
ConditionsYield
With lithium aluminium tetrahydride In diethyl ether
1-aminooctadecane
124-30-1

1-aminooctadecane

N-octadecyl-propane-1,3-diamine
4253-76-3

N-octadecyl-propane-1,3-diamine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
2: Raney nickel; ethanol / 95 °C / 14710.2 Torr / Hydrogenation
View Scheme
N-Octadecyl-3-phthalimidylpropionamid
56426-60-9

N-Octadecyl-3-phthalimidylpropionamid

N-octadecyl-propane-1,3-diamine
4253-76-3

N-octadecyl-propane-1,3-diamine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: aq. N2H4 / ethanol
2: LiAlH4 / diethyl ether
View Scheme
bis(diethoxyphosphoryl)disulphide
2901-90-8

bis(diethoxyphosphoryl)disulphide

N-octadecyl-propane-1,3-diamine
4253-76-3

N-octadecyl-propane-1,3-diamine

Bis-(N,N'-diethyl-N-octadecyl-trimethylendiammonium)-bis-(bis-O-ethyl-thiophosphono)-disulfid
101675-60-9

Bis-(N,N'-diethyl-N-octadecyl-trimethylendiammonium)-bis-(bis-O-ethyl-thiophosphono)-disulfid

Conditions
ConditionsYield
In benzene
S-ethyl O,O-dimethyl phosphorodithioate
3347-21-5

S-ethyl O,O-dimethyl phosphorodithioate

N-octadecyl-propane-1,3-diamine
4253-76-3

N-octadecyl-propane-1,3-diamine

N-Methyl-N'-octadecyl-trimethylendiammonium-O-methyl-S-ethyl-dithiophosphat
930-06-3

N-Methyl-N'-octadecyl-trimethylendiammonium-O-methyl-S-ethyl-dithiophosphat

Conditions
ConditionsYield
In benzene
S-ethyl O,O-dimethyl phosphorodithioate
3347-21-5

S-ethyl O,O-dimethyl phosphorodithioate

N-octadecyl-propane-1,3-diamine
4253-76-3

N-octadecyl-propane-1,3-diamine

N,N'-Dimethyl-N-octadecyl-trimethylendiammonium-bis-(O-methyl-S-ethyl)-dithiophosphat
4221-23-2

N,N'-Dimethyl-N-octadecyl-trimethylendiammonium-bis-(O-methyl-S-ethyl)-dithiophosphat

Conditions
ConditionsYield
In benzene
demeton-O-methyl
867-27-6

demeton-O-methyl

N-octadecyl-propane-1,3-diamine
4253-76-3

N-octadecyl-propane-1,3-diamine

N,N'-Dimethyl-N-octadecyl-trimethylendiammonium-bis-O-methyl-O-(2-ethylmercapto-ethyl)-thiophosphat
1448-34-6

N,N'-Dimethyl-N-octadecyl-trimethylendiammonium-bis-O-methyl-O-(2-ethylmercapto-ethyl)-thiophosphat

Conditions
ConditionsYield
In benzene
N-octadecyl-propane-1,3-diamine
4253-76-3

N-octadecyl-propane-1,3-diamine

Dimethoate
60-51-5

Dimethoate

N-Methyl-N'-octadecyl-trimethylendiammonium-O-methyl-S-methylcarbamoylmethyl-dithiophosphat
4221-19-6

N-Methyl-N'-octadecyl-trimethylendiammonium-O-methyl-S-methylcarbamoylmethyl-dithiophosphat

Conditions
ConditionsYield
In benzene
N-octadecyl-propane-1,3-diamine
4253-76-3

N-octadecyl-propane-1,3-diamine

Dimethoate
60-51-5

Dimethoate

N,N'-Dimethyl-N-octadecyl-trimethylendiammonium-bis-(O-methyl-S-methylcarbamoylmethyl)-dithiophosphat
96591-11-6

N,N'-Dimethyl-N-octadecyl-trimethylendiammonium-bis-(O-methyl-S-methylcarbamoylmethyl)-dithiophosphat

Conditions
ConditionsYield
In benzene
N-octadecyl-propane-1,3-diamine
4253-76-3

N-octadecyl-propane-1,3-diamine

Monothiophosphorsaeure-O,O-dimethyl-O-(2,4,5-trichlor-phenylester)
299-84-3

Monothiophosphorsaeure-O,O-dimethyl-O-(2,4,5-trichlor-phenylester)

N,N'-Dimethyl-N-octadecyl-trimethylendiammonium-bis-

N,N'-Dimethyl-N-octadecyl-trimethylendiammonium-bis-

Conditions
ConditionsYield
In benzene Heating;
N-octadecyl-propane-1,3-diamine
4253-76-3

N-octadecyl-propane-1,3-diamine

Trichlorometaphos-3
2633-54-7

Trichlorometaphos-3

N-Octadecyl-N'-methyl-trimethylendiammonium-

N-Octadecyl-N'-methyl-trimethylendiammonium-

Conditions
ConditionsYield
In benzene
N-octadecyl-propane-1,3-diamine
4253-76-3

N-octadecyl-propane-1,3-diamine

Trichlorometaphos-3
2633-54-7

Trichlorometaphos-3

N,N'-Dimethyl-N-octadecyl-trimethylendiammonium-bis-

N,N'-Dimethyl-N-octadecyl-trimethylendiammonium-bis-

Conditions
ConditionsYield
In benzene
N-octadecyl-propane-1,3-diamine
4253-76-3

N-octadecyl-propane-1,3-diamine

O-ethyl O-methyl O-p-nitrophenylthiophosphate
2591-57-3

O-ethyl O-methyl O-p-nitrophenylthiophosphate

N,N'-Dimethyl-N-octadecyl-trimethylendiammonium-bis-O-ethyl-O-(4-nitro-phenyl)-thiophosphat
1064-62-6

N,N'-Dimethyl-N-octadecyl-trimethylendiammonium-bis-O-ethyl-O-(4-nitro-phenyl)-thiophosphat

Conditions
ConditionsYield
In benzene
N-octadecyl-propane-1,3-diamine
4253-76-3

N-octadecyl-propane-1,3-diamine

acrylonitrile
107-13-1

acrylonitrile

C30H56N2

C30H56N2

Conditions
ConditionsYield
at 60 - 95℃; for 7h;
formaldehyd
50-00-0

formaldehyd

N-octadecyl-propane-1,3-diamine
4253-76-3

N-octadecyl-propane-1,3-diamine

5-ethylbenzotriazole

5-ethylbenzotriazole

C12H27O2PS2

C12H27O2PS2

C43H82N5O2PS2

C43H82N5O2PS2

Conditions
ConditionsYield
at 100℃; for 4h; Inert atmosphere;

4253-76-3Relevant articles and documents

Efficient Innate Immune Killing of Cancer Cells Triggered by Cell-Surface Anchoring of Multivalent Antibody-Recruiting Polymers

Uvyn, Annemiek,De Coen, Ruben,Gruijs, Mandy,Tuk, Cees W.,De Vrieze, Jana,van Egmond, Marjolein,De Geest, Bruno G.

supporting information, p. 12988 - 12993 (2019/08/01)

Binding of monoclonal antibodies (mAbs) onto a cell surface triggers antibody-mediated effector killing by innate immune cells through complement activation. As an alternative to mAbs, synthetic systems that can recruit endogenous antibodies from the blood stream to a cancer cell surface could be of great relevance. Herein, we explore antibody-recruiting polymers (ARPs) as a novel class of immunotherapy. ARPs consist of a cell-binding motif linked to a polymer that contains multiple small molecule antibody-binding motifs along its backbone. As a proof of concept, we employ a lipid anchor that inserts into the phospholipid cell membrane and make use of a polymeric activated ester scaffold onto which we substitute dinitrophenol as an antibody-binding motif. We demonstrate that ARPs allow for high avidity antibody binding and drive antibody recruitment to treated cells for several days. Furthermore, we show that ARP-treated cancer cells are prone to antibody-mediated killing through phagocytosis by macrophages.

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