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1120-49-6

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1120-49-6 Usage

Chemical Properties

white solid

Uses

Didecylamine is a nitrogen containing organic building blocks. It is also shown to be used as a substrate for the growth of gram-negative Pseudomonas sp bacteria obtained from the activated sludge.

Purification Methods

Dissolve the amine in *benzene and precipitate it as its bisulfate by shaking with 4M H2SO4. Filter, wash with *benzene, separate by centrifugation, then the free base is obtained by treating with NaOH [McDowell & Allen J Phys Chem 65 1358 1961]. It is a strong base; store away from CO2. [Beilstein 4 IV 780.]

Check Digit Verification of cas no

The CAS Registry Mumber 1120-49-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1120-49:
(6*1)+(5*1)+(4*2)+(3*0)+(2*4)+(1*9)=36
36 % 10 = 6
So 1120-49-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H43N/c1-3-5-7-9-11-13-15-17-19-21-20-18-16-14-12-10-8-6-4-2/h21H,3-20H2,1-2H3

1120-49-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Didecylamine

1.2 Other means of identification

Product number -
Other names 1-Decanamine, N-decyl-

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:1120-49-6 SDS

1120-49-6Relevant articles and documents

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Jung,M.E.,Lyster,M.A.

, p. 315 - 316 (1978)

-

Serum Compatible Spermine-Based Cationic Lipids with Nonidentical Hydrocarbon Tails Mediate High Transfection Efficiency

Thongbamrer, Chopaka,Roobsoong, Wanlapa,Sattabongkot, Jetsumon,Opanasopit, Praneet,Yingyongnarongkul, Boon-ek

, (2022/02/03)

Cationic lipids are widely used as nonviral synthetic vectors for gene delivery as a safer alternative to viral vectors. In this work, a library of L-shaped spermine-based cationic lipids with identical and nonidentical hydrophobic chains having variable carbon lengths (from C10 to C18) was designed and synthesized. These lipids were characterized and the structure-activity relationships of these compounds were determined for DNA binding and transfection ability when formulated as cationic liposomes. The liposomes were then used successfully for the transfection of HEK293T, HeLa, PC3, H460, HepG2, SH-SY5Y and Calu’3 cell lines. The transfection efficiency of lipids with nonidentical hydrocarbon chains was greater than the identical analogue. These reagents exhibited superior efficiency to the commercial reagent, Lipofectamine3000, under both serum-free and 10–40 % serum conditions in HEK293T, HeLa and H460 cell lines. The lipids were not toxic to the tested cell line. The results suggest that L-shaped spermine-based cationic lipids with nonidentical hydrocarbon tails could serve as efficient and safe nonviral vector gene carriers in further in vivo studies.

Selective Transformations of Triglycerides into Fatty Amines, Amides, and Nitriles by using Heterogeneous Catalysis

Jamil, Md. A. R.,Siddiki, S. M. A. Hakim,Touchy, Abeda Sultana,Rashed, Md. Nurnobi,Poly, Sharmin Sultana,Jing, Yuan,Ting, Kah Wei,Toyao, Takashi,Maeno, Zen,Shimizu, Ken-ichi

, p. 3115 - 3125 (2019/04/26)

The use of triglycerides as an important class of biomass is an effective strategy to realize a more sustainable society. Herein, three heterogeneous catalytic methods are reported for the selective one-pot transformation of triglycerides into value-added chemicals: i) the reductive amination of triglycerides into fatty amines with aqueous NH3 under H2 promoted by ZrO2-supported Pt clusters; ii) the amidation of triglycerides under gaseous NH3 catalyzed by high-silica H-beta (Hβ) zeolite at 180 °C; iii) the Hβ-promoted synthesis of nitriles from triglycerides and gaseous NH3 at 220 °C. These methods are widely applicable to the transformation of various triglycerides (C4–C18 skeletons) into the corresponding amines, amides, and nitriles.

Selective Synthesis of Primary Amines from Nitriles under Hydrogenation Conditions

Yoshimura, Masatoshi,Komatsu, Akira,Niimura, Masaru,Takagi, Yukio,Takahashi, Tohru,Ueda, Shun,Ichikawa, Tomohiro,Kobayashi, Yutaka,Okami, Hiroki,Hattori, Tomohiro,Sawama, Yoshinari,Monguchi, Yasunari,Sajiki, Hironao

, p. 1726 - 1732 (2018/03/21)

The hydrogenation of aliphatic nitriles over Pd/C, Pd/Al2O3, and Pd?Au/Al2O3 catalysts were evaluated for the selective hydrogenation of aliphatic nitriles to the corresponding primary amines. The highest selectivity (>99%) toward primary amines was achieved when the reaction was carried out in acetic acid using 10 mol% of 25% Pd-5% Au/Al2O3 under relatively low hydrogen pressure (0.8 MPa). Characterization of the catalysts by XRD, CO adsorption experiments, and EXAFS revealed that the excellent selectivity of 25% Pd-5% Au/Al2O3 toward the synthesis of primary amines is determined by the electronic properties and/or the surface structure resulting from alloying Pd with Au. (Figure presented.).

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