N-Methylbenzylamine | CAS:103-67-3 | Manufacturer ChemFaces

N-Methylbenzylamine

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According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.

Size /Price /Stock	10 mM * 1 mL in DMSO / Inquiry
Other Packaging	*Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap

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N-Methylbenzylamine Description

Source:	The herbs of Moringa oleifera
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage:	Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C). Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
After receiving:	The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.

Structure Identification:

Chinese Journal of Chemical Physics, 2004, 17(1):61-64.

Photochemical reactions of Hypocrellin A with dibenzylamine and N-methylbenzylamine.[Reference: WebLink]

METHODS AND RESULTS:
In order to discuss the free radicals formation me ch anism of Hypocrellin A (HA) with amino derivatives, the electron-spin resonance (ESR) spectroscopy was adopted to study the photochemistry on HA with dibenzyl amine (DBA) and N-Methylbenzylamine (NMBA), respectively. When HA with DBA or NMBA in chloroform solution was illuminated with visible light, singlet oxygen, semiquinone radical and oxynitride radical were formed depending on the conditi on of the solvent system containing the amino-substituted and solved oxygen. Th e signal intensity of oxynitride radical decreased with increasing the illuminat ion time, and the signal intensity of semiquinone radical increased with increas ing the illumination time. The oxynitride radical content was in inverse ratio w ith the semiquinone radical generated by being irradiated.
CONCLUSIONS:
In the aerobic system of chloroform solution containing DBA/HA, smiquinone radical was the main radic al irradiated. The results indicated that HA induced amino derivatives into HA s emiquinone radical.

Product Name	N-Methylbenzylamine
Price:
CAS No.:	103-67-3
Catalog No.:	CFN00065
Molecular Formula:	C₈H₁₁N
Molecular Weight:	121.18 g/mol
Purity:	>=98%
Type of Compound:	Alkaloids
Physical Desc.:	Oil
Source:	The herbs of Moringa oleifera
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download:	COA MSDS
Similar structural:	Comparison (Web) (SDF)
Guestbook:

Size /Price /Stock	10 mM * 100 uL in DMSO / Inquiry / In-stock 10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries	Alkaloids Compound Library

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	8.2522 mL	41.2609 mL	82.5219 mL	165.0437 mL	206.3047 mL
5 mM	1.6504 mL	8.2522 mL	16.5044 mL	33.0087 mL	41.2609 mL
10 mM	0.8252 mL	4.1261 mL	8.2522 mL	16.5044 mL	20.6305 mL
50 mM	0.165 mL	0.8252 mL	1.6504 mL	3.3009 mL	4.1261 mL
100 mM	0.0825 mL	0.4126 mL	0.8252 mL	1.6504 mL	2.063 mL

CFN00054	Muricatide	111025-01-5	283.33	C₁₇H₁₇NO₃
CFN00064	Benzylamine	100-46-9	107.15	C₇H₉N
CFN00065	N-Methylbenzylamine	103-67-3	121.18	C₈H₁₁N
CFN00079	2-Hydroxybenzylamine	932-30-9	123.15	C₇H₉NO
CFN00080	3-Hydroxybenzylamine	73604-31-6	123.15	C₇H₉NO
CFN00081	4-Hydroxybenzylamine	696-60-6	123.15	C₇H₉NO
CFN89344	Niazinin	147821-57-6	343.39	C₁₅H₂₁NO₆S
CFN89363	Niazimicin	147821-49-6	357.42	C₁₆H₂₃NO₆S
CFN96998	Niazirin	122001-32-5	279.29	C₁₄H₁₇NO₅
CFN89445	Moringin	73255-40-0	311.35	C₁₄H₁₇NO₅S