N, N- DiMethylbenzylaMine(BDMA)


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  • N, N- DiMethylbenzylaMine(BDMA)
  • 103-83-3
  • C9H13N
  • 135.209
  • Colourless to light yellow liquid
Inquiry

Factory Sells Best Quality N, N- DiMethylbenzylaMine(BDMA) 103-83-3 with GMP standards

  • Molecular Formula:C9H13N
  • Molecular Weight:135.209
  • Appearance/Colour:Colourless to light yellow liquid 
  • Vapor Pressure:0.871mmHg at 25°C 
  • Melting Point:-75 °C 
  • Refractive Index:n20/D 1.501(lit.)  
  • Boiling Point:181 °C at 760 mmHg 
  • PKA:pK1:9.02(+1) (25°C) 
  • Flash Point:130 °F 
  • PSA:3.24000 
  • Density:0.9 g/mL at 25 °C(lit.) 
  • LogP:1.74820 

N,N-Dimethylbenzylamine(Cas 103-83-3) Usage

Preparation

25% Aqueous Dimethylamine, 1088 grams Benzyl Chloride, 126.6 grams In the apparatus of Example 1, the benzyl chloride was added dropwise over a two-hour period to the amine (molar ratio 1 to 6) at a rate sufficient to maintain the temperature below 40°C. Stirring was continued at room temperature for an additional hour to insure completion of the reaction denoted by the equation below. Thereafter the reaction mixture was cooled in a separatory funnel while standing in a refrigerator maintained at 5° C. and separated into two layers. The upper oily layer, weighing 111.5g, was removed and steam distilled until no further oleaginous component was observed in the distillate as it came over. The crude distillate was found to contain 103.5g of N,N-dimethylbenzylamine (76.1% of theory), 3.3g of dimethylamine and no quaternary salts. The dimethylamine was distilled off below 29°C under atmospheric pressure from the N,N-dimethylbenzylamine (bp 82°C/18mmHg).

Synthesis Reference(s)

The Journal of Organic Chemistry, 40, p. 531, 1975 DOI: 10.1021/jo00892a043Synthetic Communications, 6, p. 539, 1976 DOI: 10.1080/00397917608063545

Air & Water Reactions

Flammable. Slightly soluble in water.

Reactivity Profile

N,N-Dimethylbenzylamine neutralizes acids on exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. May attack some plastics [USCG, 1999].

Health Hazard

Inhalation may be fatal as a result of spasm, inflammation and edema of the larynx and bronchi, chemical pneumonitis, and pulmonary edema. Symptoms of exposure may include burning sensation, coughing, wheezing, laryngitis, shortness of breath, headache, nausea, and vomitting.

Fire Hazard

Special Hazards of Combustion Products: Toxic vapors are generated when heated.

Flammability and Explosibility

Flammable

Safety Profile

Poison by ingestion. Moderately toxic by inhalation and skin contact. Corrosive. A severe eye and skin irritant. Flammable when exposed to heat or flame. When heated to decomposition it emits toxic fumes of NOx

Purification Methods

Dry the amine over KOH pellets and fractionate it over Zn dust in a CO2—free atmosphere. It has a pKa2 5 of 8.25 in 45% aqueous EtOH. Store it under N2 or in a vacuum. The picrate has m 94-95o, and the picrolonate has m 151o (from EtOH). [Skita & Keil Chem Ber 63 34 1930, Coleman J Am Chem Soc 55 3001 1933, Devereux et al. J Chem Soc 2845 1957.] The tetraphenyl borate salt has m 182-185o. [Crane Anal Chem 28 1794 1956, Beilstein 12 IV 2161.]

General Description

A colorless to light yellow liquid with an aromatic odor. Slightly less dense than water and slightly soluble in water. Flash point approximately 140°F. Corrosive to skin, eyes and mucous membranes. Slightly toxic by ingestion, skin absorption and inhalation. Used in the manufacture of adhesives and other chemicals.

InChI:InChI=1/C9H13N/c1-10(2)8-9-6-4-3-5-7-9/h3-7H,8H2,1-2H3/p+1

103-83-3 Relevant articles

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Iversen

, p. 55 (1971)

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B(C6F5)3-catalyzed methylation of amines using CO2 as a C1 building block

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B(C6F5)3 was proven to be an efficient m...

Reductive Alkylations of Dimethylamine Using Titanium(IV) Isopropoxide and Sodium Borohydride: An Efficient, Safe, and Convenient Method for the Synthesis of N,N-Dimethylated Tertiary Amines

Bhattacharyya, Sukanta

, p. 4928 - 4929 (1995)

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Van Koten et al.

, p. 2047,2049, 2052 (1977)

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Bis- n -heterocyclic carbene (nhc) stabilized η6-arene iron(0) complexes: Synthesis, structure, reactivity, and catalytic activity

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, p. 12591 - 12600 (2017)

Representative tertiary amines were link...

Reaction of alkyl sulfoxides and phenylphosphinic acid with amines. Alternative reagents for secondary amines N-alkylation

Chauvin

, p. 1425 - 1428 (1991)

Phenylphosphinic acid and dialkylsulfoxi...

Borinic Acid Catalysed Reduction of Tertiary Amides with Hydrosilanes: A Mild and Chemoselective Synthesis of Amines

Chardon, Aurélien,Mohy El Dine, Tharwat,Legay, Rémi,De Paolis, Micha?l,Rouden, Jacques,Blanchet, Jér?me

, p. 2005 - 2009 (2017)

A reduction of various aryl, alkyl, and ...

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, p. 13326 - 13329 (2016)

Triphenylborane (BPh3) was found to cata...

Base-promoted elimination reactions of acetaldehyde N-alkyl-N,N-dimethylhydrazonium salts. A convenient synthesis of N,N-dimethylalkylamines

Smith,Marcucci,Tingue

, p. 381 - 389 (1992)

The title reaction was utilized for effi...

Efficient and Selective N-Methylation of Nitroarenes under Mild Reaction Conditions

Pedrajas, Elena,Sorribes, Iván,Guillamón, Eva,Junge, Kathrin,Beller, Matthias,Llusar, Rosa

, p. 13205 - 13212 (2017)

Herein, we report a straightforward prot...

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Proni et al.

, p. 47 (1977)

-

Base-Catalyzed Hydrosilylation of Nitriles to Amines and Esters to Alcohols

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, p. 4434 - 4439 (2021)

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, p. 11576 - 11579 (2015)

Azo-functionalized MOPs (Azo-MOPs) were ...

Lithium compound catalyzed deoxygenative hydroboration of primary, secondary and tertiary amides

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, p. 2354 - 2358 (2021)

A selective and efficient route for the ...

Synthesis of N,N-dimethylamines via Barbier-Grignard-type electrophilic amination

Erdik, Ender,Ates, Selma

, p. 2813 - 2818 (2006)

Aryl Grignard reagents react with N,N-di...

Self-encapsulation of homogeneous catalyst species into polymer gel leading to a facile and efficient separation system of amine products in the Ru-catalyzed reduction of carboxamides with polymethylhydrosiloxane (PMHS)

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, p. 13150 - 13151 (2005)

A practical procedure for production of ...

Fast N-methylation of amines under microwave irradiation

Barbry, Didier,Torchy, Severine

, p. 3919 - 3922 (1996)

Primary and secondary amines are quickly...

Transformation of Monoamine Oxidase-B Primary Amine Substrates into Time-Dependent Inhibitors. Tertiary Amine Homologues of Primary AMine Substrates

Ding, Charles Z.,Lu, Xingliang,Nishimura, Kuniko,Silverman, Richard B.

, p. 1711 - 1715 (1993)

A family of N-methylated and N,N-dimethy...

-

Van Koten,Noltes

, p. 452,453 (1972)

-

Studies into reactions of N-methylmorpholine-N-oxide (NMMO) and its hydrates with cyanuric chloride

Rosenau, Thomas,Potthast, Antje,Kosma, Paul

, p. 9809 - 9815 (2002)

The course of the reaction between N-met...

Transition metal-free methylation of amines with formaldehyde as the reductant and methyl source

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, p. 345 - 347 (2015)

A simple transition metal-free procedure...

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Mistryukov, Electron A.

, p. 230 - 231 (2002)

The addition of tert-butyl borate or eth...

Thermal Decomposition of Dimethylnitramine and Dimethylnitrosamine by Pulsed Laser Pyrolysis

Nigenda, S. Esther,McMillen, Donald F.,Golden, David M.

, p. 1124 - 1130 (1989)

Pyrolysis of dimethylnitramine (DMNA) an...

Simple Amine-Directed Meta-Selective C-H Arylation via Pd/Norbornene Catalysis

Dong, Zhe,Wang, Jianchun,Dong, Guangbin

, p. 5887 - 5890 (2015)

Herein we report a highly meta-selective...

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, p. 6264 - 6267 (2014)

Pt and MoOx co-loaded TiO2 is found to b...

N,N-Diethylaniline·borane, an efficient reducing agent for reduction of representative functional groups

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, p. 1519 - 1522 (1997)

N,N-Diethylaniline·borane (DEANB), a the...

Experimental and computational studies of borohydride catalyzed hydrosilylation of a variety of C=O and C=N functionalities including esters, amides and heteroarenes

Manas, Michael G.,Sharninghausen, Liam S.,Balcells, David,Crabtree, Robert H.

, p. 1694 - 1700 (2014)

Sodium borohydride and a series of relat...

Mild and Efficient Flavin-Catalyzed H2O2 Oxidation of Tertiar Amines to Amine N-Oxides

Bergstad, Katarina,B?ckvall, Jan-E.

, p. 6650 - 6655 (1998)

A mild and highly effective H2O2 oxidati...

-

Cooke,Parlman

, p. 531 (1975)

-

-

Saunders,Murray

, p. 1,8 (1960)

-

Formation of octahedral iridium(III) dihydrides from the reaction of ortho-chelated aryliridium(I) compounds with dihydrogen

Van Der Zeijden, Adolphus A. H.,Van Koten, Gerard,Luijk, Ronald,Grove, David M.

, p. 1556 - 1561 (1988)

The reaction of IrI[C6H2(CH2NMe 2)-2-R1-...

Reductive methylation using decaborane in methanol

Yeon Joo Jung,Jong Woo Bae,Choon-Ock Maing Yoon,Byung Woo Yoo,Cheol Min Yoon

, p. 3417 - 3421 (2001)

Amines (primary and secondary) were meth...

A novel strategy for oligopeptide synthesis using a polymer-supported ammonium fluoride

Kurosu, Michio,Crick, Dean C.

, p. 5325 - 5328 (2006)

A novel method for the preparation of ol...

Dual antitumor and antiangiogenic activity of organoplatinum(II) complexes

Zamora, Ana,Pérez, Sergio A.,Rodríguez, Venancio,Janiak, Christoph,Yellol, Gorakh S.,Ruiz, José

, p. 1320 - 1336 (2015)

A library of over 20 cycloplatinated com...

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Kapicak,Gabbay

, p. 403,404, 405 (1975)

-

MANNICH REACTIONS OF ARYL-TRIALKYLSTANNANES USING PREFORMED DIALKYL-METHYLENEIMINIUM SALTS

Cooper, Mark S.,Heaney Harry

, p. 5011 - 5014 (1986)

Dialkyl-methyleneiminium salts react wit...

Additive-free selective methylation of secondary amines with formic acid over a Pd/In2O3 catalyst

Benaissa, Idir,Cantat, Thibault,Genre, Caroline,Godou, Timothé,Pinault, Mathieu

, p. 57 - 61 (2022/01/19)

Formic acid is used as the sole carbon a...

BF3·Et2O as a metal-free catalyst for direct reductive amination of aldehydes with amines using formic acid as a reductant

Fan, Qing-Hua,Liu, Xintong,Luo, Zhenli,Pan, Yixiao,Xu, Lijin,Yang, Ji,Yao, Zhen,Zhang, Xin

supporting information, p. 5205 - 5211 (2021/07/29)

A versatile metal- and base-free direct ...

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, reusa...

Method for preparing tertiary amine organic compound from photocatalytically decomposing substituted formamide

-

Paragraph 0026-0028, (2021/01/12)

The invention discloses a method for pre...

103-83-3 Process route

2-chloro-benzaldehyde
89-98-5

2-chloro-benzaldehyde

dimethyl amine
124-40-3

dimethyl amine

N,N'-dimethylbenzylamine
103-83-3

N,N'-dimethylbenzylamine

2-Chlorobenzyl alcohol
17849-38-6

2-Chlorobenzyl alcohol

1-(2-chlorophenyl)-N,N-dimethylmethanamine
10175-31-2

1-(2-chlorophenyl)-N,N-dimethylmethanamine

Conditions
Conditions Yield
With acetic acid; In water; at 99.84 ℃; for 3h; under 3750.38 Torr; Inert atmosphere;
N,N-dimethylthiobenzamide
15482-60-7

N,N-dimethylthiobenzamide

N,N'-dimethylbenzylamine
103-83-3

N,N'-dimethylbenzylamine

dibenzyl disulphide
150-60-7

dibenzyl disulphide

phenylmethanethiol
100-53-8

phenylmethanethiol

Conditions
Conditions Yield
With sodium tetrahydroborate; In acetonitrile; for 26h; Heating;
6%
23%
63%

103-83-3 Upstream products

  • 50-00-0
    50-00-0

    formaldehyd

  • 64-18-6
    64-18-6

    formic acid

  • 706-03-6
    706-03-6

    3-(benzylamino)propionitrile

  • 5400-93-1
    5400-93-1

    1-benzyl-3,5,7-triaza-1-azoniatricyclo<3,3,1,13,7>decane chloride

103-83-3 Downstream products

  • 120-51-4
    120-51-4

    benzoic acid benzyl ester

  • 84555-07-7
    84555-07-7

    benzyl-butoxycarbonylmethyl-dimethyl-ammonium; chloride

  • 5467-99-2
    5467-99-2

    4-methylbenzoic acid benzyl ester

  • 120383-72-4
    120383-72-4

    benzyl-dimethyl-phenoxycarbonylmethyl-ammonium; chloride

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