Grouped product items

SKU

Size

Availability

Price

Qty

D110950-25ml

25ml

In stock

$9.90

D110950-100ml

100ml

In stock

$25.90

D110950-500ml

500ml

Available within 4-8 weeks(?)

$86.90

Basic Description

Synonyms	N,N-DIMETHYLBENZYLAMINE\|103-83-3\|Benzyldimethylamine\|N-Benzyldimethylamine\|N,N-dimethyl-1-phenylmethanamine\|Dimethylbenzylamine\|BDMA\|Benzenemethanamine, N,N-dimethyl-\|Benzyl-N,N-dimethylamine\|N-(Phenylmethyl)dimethylamine\|N,N-Dimethylbenzenemethanamine\|Ar
Specifications & Purity	≥99%
Storage Temp	Store at 2-8°C,Argon charged
Shipped In	Wet ice
Product Description	Description N,N-Dimethylbenzylamine reacts with Os3(CO)12 to form triosmium clusters. Anodic oxidation of N,N-dimethylbenzylamine has been studied in methanol-tetra-n-butylammonium fluoroborate and in methanol-potassium hydroxide. Application N,N-Dimethylbenzylamine is used in the preparation of bis[(N,N-dimethylamino)benzyl] selenide. It acts as a catalyst in the curing reaction of formulations of diglycidyl ether of bisphenol A and tetrahydrophthalic anhydride. It undergoes directed ortho metalation with butyl lithium. It reacts with methyl iodide to get ammonium salt, which is used as phase transfer catalysts. Further, it is used as a catalyst for the formation of polyurethane foams and epoxy resins.

Associated Targets

VDR Tclin Vitamin D3 receptor 0 Activities

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

TSHR Tclin Thyrotropin receptor 0 Activities

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

MAOB Tclin Amine oxidase [flavin-containing] B 0 Activities

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

ALDH1A1 Tchem Retinal dehydrogenase 1 0 Activities

Discover Target: ALDH1A1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Names and Identifiers

IUPAC Name	N,N-dimethyl-1-phenylmethanamine
INCHI	InChI=1S/C9H13N/c1-10(2)8-9-6-4-3-5-7-9/h3-7H,8H2,1-2H3
InChi Key	XXBDWLFCJWSEKW-UHFFFAOYSA-N
Canonical SMILES	CN(C)CC1=CC=CC=C1
Isomeric SMILES	CN(C)CC1=CC=CC=C1
WGK Germany	2
RTECS	DP4500000
PubChem CID	7681
UN Number	2619
Packing Group	II
Molecular Weight	135.21
Beilstein	1099620
Reaxy-Rn	1099620

Certificates

Certificate of Analysis(COA)

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26 results found

Lot Number	Certificate Type	Date	Item
H2423013	Certificate of Analysis	Sep 07, 2024	D110950
I2404049	Certificate of Analysis	Aug 26, 2024	D110950
I2404048	Certificate of Analysis	Aug 26, 2024	D110950
I2404037	Certificate of Analysis	Aug 26, 2024	D110950
F2415080	Certificate of Analysis	Jun 24, 2024	D110950
C2412028	Certificate of Analysis	Mar 20, 2024	D110950
D2407206	Certificate of Analysis	Mar 13, 2024	D110950
D2407208	Certificate of Analysis	Mar 13, 2024	D110950
L2315492	Certificate of Analysis	Nov 30, 2023	D110950
L2315491	Certificate of Analysis	Nov 30, 2023	D110950
K2308038	Certificate of Analysis	Nov 16, 2023	D110950
I2322097	Certificate of Analysis	Sep 28, 2023	D110950
F23161104	Certificate of Analysis	Jun 09, 2023	D110950
F23161101	Certificate of Analysis	Jun 09, 2023	D110950
F23161165	Certificate of Analysis	Jun 09, 2023	D110950
F23161164	Certificate of Analysis	Jun 09, 2023	D110950
F23161163	Certificate of Analysis	Jun 09, 2023	D110950
F23161106	Certificate of Analysis	Jun 09, 2023	D110950
F23161103	Certificate of Analysis	Jun 09, 2023	D110950
H2224175	Certificate of Analysis	Aug 11, 2022	D110950
H2224176	Certificate of Analysis	Aug 11, 2022	D110950
H2224179	Certificate of Analysis	Aug 11, 2022	D110950
H2224180	Certificate of Analysis	Aug 11, 2022	D110950
F23171155	Certificate of Analysis	Aug 11, 2022	D110950
D2304489	Certificate of Analysis	Aug 11, 2022	D110950
B2218006	Certificate of Analysis	Nov 18, 2021	D110950

Chemical and Physical Properties

Solubility	Slightly miscible with water.
Sensitivity	Air sensitive
Refractive Index	1.501
Flash Point(°F)	129°F
Flash Point(°C)	54℃
Boil Point(°C)	183-184°C
Melt Point(°C)	-75°C

Safety and Hazards(GHS)

Pictogram(s)	GHS05, GHS07, GHS02
Signal	Danger
Hazard Statements	H314:Causes severe skin burns and eye damage H412:Harmful to aquatic life with long lasting effects H302:Harmful if swallowed H312:Harmful in contact with skin H226:Flammable liquid and vapor H332:Harmful if inhaled
Precautionary Statements	P261:Avoid breathing dust/fume/gas/mist/vapors/spray. P273:Avoid release to the environment. P280:Wear protective gloves/protective clothing/eye protection/face protection. P370+P378:In case of fire: Use ... to extinguish. P210:Keep away from heat, hot surface, sparks, open flames and other ignition sources. - No smoking. P302+P352:IF ON SKIN: wash with plenty of water. P321:Specific treatment (see ... on this label). P405:Store locked up. P501:Dispose of contents/container to ... P233:Keep container tightly closed. P240:Ground/bond container and receiving equipment. P264:Wash hands [and …] thoroughly after handling. P403+P235:Store in a well-ventilated place. Keep cool. P260:Do not breathe dust/fume/gas/mist/vapors/spray. P303+P361+P353:IF ON SKIN (or hair): Take off Immediately all contaminated clothing. Rinse SKIN with water [or shower]. P271:Use only outdoors or in a well-ventilated area. P241:Use explosion-proof [electrical/ventilating/lighting/.../] equipment. P270:Do not eat, drink or smoke when using this product. P301+P330+P331:IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing. P363:Wash contaminated clothing before reuse. P362+P364:Take off contaminated clothing and wash it before reuse. P330:Rinse mouth. P242:Use only non-sparking tools. P243:Take precautionary measures against static discharge. P301+P317:IF SWALLOWED: Get medical help. P305+P354+P338:IF IN EYES: Immediately rinse with water for several minutes. Remove contact lenses if present and easy to do. Continue rinsing. P317:Get emergency medical help. P302+P361+P354:IF ON SKIN: Take off Immediately all contaminated clothing. Immediately rinse with water for several minutes. P316:Get emergency medical help immediately.
WGK Germany	2
RTECS	DP4500000
Reaxy-Rn	1099620
Class	8, 3

Alternative Products

References

1. F Pautet,R Barret,M Daudon. (1988-01-01) [Optimization of biomimetic oxidation reactions achieved with the aid of an iodosylbenzene and meso-tetraphenylporphinatoiron (III): application to antergan].. Pharmaceutica acta Helvetiae, 63 ((4-5)): (140-144). [PMID:3222268]
2. L P Novitskaia,A Ia Lutsenko,V D Chmil. (1993-11-01) [Thin-layer chromatographic method for determination of N,N-dimethylbenzilamine in the air during sanitary and chemical studies of polymers].. Gigiena i sanitariia, ((11)(11)): (63-64). [PMID:8307416]
3. B Ståhlbom,B Akesson,B Jönsson. (1997-01-01) Experimental human exposure to N,N-dimethylbenzylamine: generation of a controlled atmosphere and biological monitoring.. International archives of occupational and environmental health, 70 ((6)): (393-398). [PMID:9439985]
4. D E Edmondson. (1999-03-05) Benzylamine analog binding studies as probes of the substrate sites of monoamine oxidases A and B.. Drug metabolism reviews, 31 ((1)): (235-245). [PMID:10065374]
5. N Hayashi,Y Kobayashi,Y Kishi. (2001-07-07) Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: scope and limitation.. Organic letters, 3 ((14)): (2249-2252). [PMID:11440591]
6. Shuji Yasuike,Satoru Okajima,Jyoji Kurita. (2002-10-10) Synthesis of optically active organoantimony compounds having an (S)-alpha-methylbenzyldimethylamine group and its evaluation for asymmetric reaction.. Chemical & pharmaceutical bulletin, 50 ((10)): (1404-1406). [PMID:12372876]
7. Henrik Parshad,Karla Frydenvang,Tommy Liljefors,Henning Osholm Sorensen,Claus Larsen. (2003-12-31) Aqueous solubility study of salts of benzylamine derivatives and p-substituted benzoic acid derivatives using X-ray crystallographic analysis.. International journal of pharmaceutics, 269 ((1)): (157-168). [PMID:14698587]
8. Bruno Bard,Pierre-Alain Carrupt,Sophie Martel. (2009-04-29) Lipophilicity of basic drugs measured by hydrophilic interaction chromatography.. Journal of medicinal chemistry, 52 ((10)): (3416-3419). [PMID:19397318]
9. Guang-Rong Peh,Eric Assen B Kantchev,Chi Zhang,Jackie Y Ying. (2009-05-08) N-heterocycle carbene (NHC)-ligated cyclopalladated N,N-dimethylbenzylamine: a highly active, practical and versatile catalyst for the Heck-Mizoroki reaction.. Organic & biomolecular chemistry, 7 ((10)): (2110-2119). [PMID:19421449]
10. Ernesto Oyervides-Muñoz,Eric Pollet,Gilles Ulrich,Gerardo de Jesús Sosa-Santillán,Luc Avérous. (2016-12-19) Original method for synthesis of chitosan-based antimicrobial agent by quaternary ammonium grafting.. Carbohydrate polymers, 157 (1922-1932). [PMID:27987912]
11. Wilson Beita-Sandí,Cagri Utku Erdem,Tanju Karanfil. (2019-12-04) Effect of bromide on NDMA formation during chloramination of model precursor compounds and natural waters.. Water research, 170 (115323-115323). [PMID:31790888]
12. J A Mascorro,G S Kirby. (1992-01-01) Designing multi-viscosity embedding media utilizing novel resin/anhydride/catalyst combinations.. Microscopy research and technique, 20 ((1)): (105-106). [PMID:1611146]
13. B Ballantyne,D E Dodd,D J Nachreiner,R C Myers. (1985-01-01) The acute toxicity and primary irritancy of N-benzyl-N,N-dimethylamine.. Drug and chemical toxicology, 8 ((1-2)): (43-56). [PMID:4017898]
14. Y Kobayashi,N Hayashi,C H Tan,Y Kishi. (2001-07-07) Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: proof of concept.. Organic letters, 3 ((14)): (2245-2248). [PMID:11440590]
15. Y Kobayashi,N Hayashi,Y Kishi. (2001-07-07) Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: NMR desymmetrization of meso compounds.. Organic letters, 3 ((14)): (2253-2255). [PMID:11440592]
16. M A Patrauchan,P J Oriel. (2003-01-22) Degradation of benzyldimethylalkylammonium chloride by Aeromonas hydrophila sp. K.. Journal of applied microbiology, 94 ((2)): (266-272). [PMID:12534818]
17. Sinbad Sweeney,Ioannis G Theodorou,Marta Zambianchi,Shu Chen,Andrew Gow,Stephan Schwander,Junfeng Jim Zhang,Kian Fan Chung,Milo S P Shaffer,Mary P Ryan,Alexandra E Porter,Teresa D Tetley. (2015-05-23) Silver nanowire interactions with primary human alveolar type-II epithelial cell secretions: contrasting bioreactivity with human alveolar type-I and type-II epithelial cells.. Nanoscale, 7 ((23)): (10398-10409). [PMID:25996248]
18. Mirjana Rodošek,Mohor Mihelčič,Marija Čolović,Ervin Šest,Matic Šobak,Ivan Jerman,Angelja K Surca. (2020-03-11) Tailored Crosslinking Process and Protective Efficiency of Epoxy Coatings Containing Glycidyl-POSS.. Polymers, 12 ((3)): [PMID:32151007]
19. Xiu Ying Yang,Ying Li,Song Qi Cai,Li Wang,Jin Wei Qiang. (2021-02-13) Optimization of 7,12-dimethylbenz(a)anthracene-induced rat epithelial ovarian tumors.. Oncology letters, 21 ((3)): (206-206). [PMID:33574945]

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N,N-Dimethylbenzylamine - 99%, high purity , CAS No.103-83-3