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N~1~,N~1~,N~3~-trimethyl-beta-alaninamide, also known as SALTDATA: FREE, is a chemical compound belonging to the beta-alaninamide family. It is a trimethylated derivative of the non-essential amino acid beta-alanine, which is naturally produced in the human body. This versatile compound has been studied for its potential neuroprotective, antioxidant, anti-inflammatory, and anti-cancer properties, making it a promising candidate for various applications in the pharmaceutical and cosmetic industries.

17268-50-7

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17268-50-7 Usage

Uses

Used in Pharmaceutical Industry:
N~1~,N~1~,N~3~-trimethyl-beta-alaninamide is used as a neuroprotective agent for its potential to treat neurological disorders and age-related cognitive decline. Its antioxidant properties also contribute to its therapeutic effects, supporting the health of brain cells and potentially slowing the progression of neurodegenerative diseases.
Used in Cosmetic Industry:
In the cosmetic industry, N~1~,N~3~-trimethyl-beta-alaninamide is used as an ingredient in various products due to its potential anti-aging and skin health benefits. Its antioxidant properties may help protect the skin from oxidative stress and environmental damage, promoting a youthful and healthy appearance.
Used in Antioxidant Applications:
N~1~,N~1~,N~3~-trimethyl-beta-alaninamide is used as an antioxidant agent for its ability to neutralize free radicals and protect cells from oxidative damage. This may be particularly beneficial in the prevention and treatment of various diseases and conditions associated with oxidative stress.
Used in Anti-inflammatory Applications:
Due to its potential anti-inflammatory properties, N~1~,N~1~,N~3~-trimethyl-beta-alaninamide may be used in applications targeting the reduction of inflammation and related symptoms in various conditions, such as arthritis or other inflammatory disorders.
Used in Anti-cancer Applications:
N~1~,N~1~,N~3~-trimethyl-beta-alaninamide is being studied for its potential anti-cancer properties, which may include the inhibition of cancer cell growth and the promotion of apoptosis in cancer cells. This could lead to its use in cancer treatment and prevention strategies in the future.

Check Digit Verification of cas no

The CAS Registry Mumber 17268-50-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,6 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17268-50:
(7*1)+(6*7)+(5*2)+(4*6)+(3*8)+(2*5)+(1*0)=117
117 % 10 = 7
So 17268-50-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H14N2O/c1-7-5-4-6(9)8(2)3/h7H,4-5H2,1-3H3

17268-50-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-3-(methylamino)propanamide

1.2 Other means of identification

Product number -
Other names BB_SC-5314

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:17268-50-7 SDS

17268-50-7Relevant academic research and scientific papers

BICYCLO HETEROCYCLIC COMPOUND HAVING ANTIFUNGAL ACTION

-

Page/Page column 173, (2008/06/13)

It is intended to provide a 1,6-β-glucan synthase inhibitor which strongly inhibits proliferation and has a high safety. It is intended to provide a compound which can specifically or selectively expressing an antifungal action on a broad spectrum based on the action mechanism of inhibiting the synthesis of 1,6-β-glucan. Further, it is intended to provide a drug, in particular, an antifungal agent containing the above compound, its salt or a hydrate thereof. More specifically speaking, a compound represented by the following general formula (I), its salt or a hydrate thereof; and a drug or an antifungal agent containing the above compound, its salt or a hydrate thereof.

The Ease of C-N bond Fission in Azetidine Derivatives

Page, Michael I.,Webster, Philip,Ghosez, Leon,Bogdan, Sophie

, p. 272 - 276 (2007/10/02)

The C-N bond in azetidine derivatives is not readily cleaved.Despite the release of strain energy accompanying endocyclic C-N bond fission, exocyclic C-N bond fission often occurs preferentially in the hydrolysis of azetidin -2-ylideneammonium salts to form a β-lactam.The ratio of β-lactam to β-aminoamide produced is pH, buffer and substituent dependent.The general acid catalysed breakdown of the neutral tetrahedral intermediate is a concerted process.'

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