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N,N-Dimethylbenzylamine - reagent grade,98.0%, high purity , CAS No.103-83-3

    Grade & Purity:
  • CP
  • ≥98%
In stock
Item Number
D110949
Grouped product items
SKU Size
Availability
Price Qty
D110949-100ml
100ml
5
$17.90
D110949-250ml
250ml
3
$38.90
D110949-500ml
500ml
2
$69.90

Basic Description

Synonyms J-523270 | MLS002222342 | Benzenemethanamine,dimethyl- | EC 203-149-1 | N, N-Dimethylbenzylamine | FT-0657620 | N-benzyl dimethylamine | N,N-Dimethylbenzylamine(Benzyldimethylamine) | NSC-5342 | SCHEMBL15900 | Benzylamine,N-dimethyl- | Benzyl-N,N-dimethyl
Specifications & Purity CP, ≥98%
Storage Temp Store at 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Grade CP
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.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Phenylmethylamines
Intermediate Tree Nodes Not available
Direct Parent Phenylmethylamines
Alternative Parents Benzylamines  Aralkylamines  Trialkylamines  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Phenylmethylamine - Benzylamine - Aralkylamine - Tertiary aliphatic amine - Tertiary amine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as phenylmethylamines. These are compounds containing a phenylmethtylamine moiety, which consists of a phenyl group substituted by an methanamine.
External Descriptors Not available

Associated Targets(Human)

VDR Tclin Vitamin D receptor (26531 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MAOB Tclin Monoamine oxidase B (8835 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

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
InChIKey XXBDWLFCJWSEKW-UHFFFAOYSA-N
Smiles CN(C)CC1=CC=CC=C1
Isomeric SMILES CN(C)CC1=CC=CC=C1
WGK Germany 2
RTECS DP4500000
UN Number 2619
Packing Group II
Molecular Weight 135.21
Beilstein 1099620
Reaxy-Rn 1099620
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1099620&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

14 results found

Lot Number Certificate Type Date Item
C2531141 Certificate of Analysis Apr 08, 2025 D110949
C2531142 Certificate of Analysis Apr 03, 2025 D110949
L2315490 Certificate of Analysis Dec 21, 2023 D110949
L2315489 Certificate of Analysis Dec 21, 2023 D110949
L1927039 Certificate of Analysis Oct 24, 2023 D110949
F23161102 Certificate of Analysis Jun 21, 2023 D110949
F23161109 Certificate of Analysis Jun 21, 2023 D110949
F23161111 Certificate of Analysis Jun 21, 2023 D110949
F23161096 Certificate of Analysis Jun 21, 2023 D110949
F23161115 Certificate of Analysis Jun 21, 2023 D110949
H2224268 Certificate of Analysis Aug 26, 2022 D110949
H2224174 Certificate of Analysis Aug 26, 2022 D110949
H2224178 Certificate of Analysis Aug 25, 2022 D110949
I1811104 Certificate of Analysis Jul 13, 2022 D110949

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Chemical and Physical Properties

Solubility Slightly soluble in cold water, soluble in hot water, and miscible with alcohol and ether.
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
Molecular Weight 135.210 g/mol
XLogP3 2.000
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 1
Rotatable Bond Count 2
Exact Mass 135.105 Da
Monoisotopic Mass 135.105 Da
Topological Polar Surface Area 3.200 Ų
Heavy Atom Count 10
Formal Charge 0
Complexity 82.700
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

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