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N,N-Dimethyl-L-Alanine, also known as CAS 770-66-1, is a chemical compound that belongs to the category of amino acids and derivatives. It is primarily used for scientific research purposes and is not commonly found in natural, biological settings. N,N-Dimethyl-L-Alanine is characterized by its white to light yellow crystalline powder appearance and its solubility in water. With a molecular formula of C5H11NO2 and a molecular weight of 117.15 g/mol, it is a stable compound that does not pose significant safety concerns. However, it is essential to handle it with care in a laboratory environment to prevent potential contact, ingestion, or inhalation risks.

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  • 157431-09-9 Structure
  • Basic information

    1. Product Name: N,N-Dimethyl-L-Alanine
    2. Synonyms: N,N-Dimethyl-L-Alanine;N,N-Dimethyl-L-Ala-OH;(S)-2-(DiMethylaMino)propanoic acid;(R)-2-(dimethylamino)propanoic acid;D-Alanine,N,N-dimethyl-
    3. CAS NO:157431-09-9
    4. Molecular Formula: C5H11NO2
    5. Molecular Weight: 117.14634
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 157431-09-9.mol
  • Chemical Properties

    1. Melting Point: 184℃
    2. Boiling Point: 179.9±23.0℃ (760 Torr)
    3. Flash Point: 62.6±22.6℃
    4. Appearance: /
    5. Density: 1.033±0.06 g/cm3 (20 ºC 760 Torr)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: N,N-Dimethyl-L-Alanine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N-Dimethyl-L-Alanine(157431-09-9)
    11. EPA Substance Registry System: N,N-Dimethyl-L-Alanine(157431-09-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 157431-09-9(Hazardous Substances Data)

157431-09-9 Usage

Uses

Used in Scientific Research:
N,N-Dimethyl-L-Alanine is used as a research compound for various scientific studies. Its unique properties and characteristics make it a valuable tool in the exploration of amino acid chemistry and related fields. N,N-Dimethyl-L-Alanine's availability and stability contribute to its widespread use in laboratory settings, where it can be employed in a range of experiments and analyses.
Used in Pharmaceutical Development:
In the pharmaceutical industry, N,N-Dimethyl-L-Alanine is used as a building block for the synthesis of various drug molecules. Its chemical structure allows for the creation of novel compounds with potential therapeutic applications. Researchers can manipulate its properties to develop new drugs or improve existing ones, making it an essential component in the drug discovery process.
Used in Chemical Synthesis:
N,N-Dimethyl-L-Alanine is also utilized in the synthesis of other chemical compounds, particularly in the field of organic chemistry. Its reactivity and compatibility with various chemical groups make it a versatile starting material for the production of a wide array of molecules. This versatility is particularly valuable in the development of new materials, catalysts, and other specialty chemicals.
Used in Analytical Chemistry:
In analytical chemistry, N,N-Dimethyl-L-Alanine serves as a reference material or a standard for the calibration of analytical instruments. Its well-defined chemical properties and purity make it an ideal candidate for use in the development and validation of analytical methods, ensuring accurate and reliable results in various applications, such as quality control, environmental monitoring, and clinical diagnostics.

Check Digit Verification of cas no

The CAS Registry Mumber 157431-09-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,4,3 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 157431-09:
(8*1)+(7*5)+(6*7)+(5*4)+(4*3)+(3*1)+(2*0)+(1*9)=129
129 % 10 = 9
So 157431-09-9 is a valid CAS Registry Number.

157431-09-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-Dimethyl-L-alanine

1.2 Other means of identification

Product number -
Other names (R)-N,N-diisopropyl-3-(2-benzyloxy-5-methyloxycarbonyl-phenyl)-3-phenylpropanamine

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:157431-09-9 SDS

157431-09-9Relevant articles and documents

SYNTHESIS OF LEVOMETHADONE HYDROCHLORIDE

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Paragraph 0081-0085, (2020/09/15)

A method for synthesizing levomethadone hydrochloride including producing (R)-2-(dimethylamino)propan-1-ol by reducing N,N-dimethyl-D-alanine using borax, forming (R)-1-chloro-N,N-dimethylpropane-2-amine hydrochloride by chlorinating the (R)-2-(dimethylamino)propan-1-ol, synthesizing levomethadone nitrile hydrochloride by mixing the (R)-1-chloro-N,N-dimethylpropane-2-amine and diphenylacetonitrile with potassium t-butoxide and producing levomethadone hydrochloride by exposing the levomethadone nitrile hydrochloride to a Grignard reagent.

SYNTHESIS OF LEVOMETHADONE HYDROCHLORIDE OR DEXTROMETHADONE HYDROCHLORIDE AND METHODS FOR USE THEREOF

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Paragraph 00300-00302, (2017/03/14)

Highly efficient methods for synthesis of levomethadone hydrochloride or dextromethadone hydrochloride are provided starting from D-alanine, or L-alanine, respectively, with retention of configuration. Methods for treating a subject are provided comprising administering a composition comprising an effective amount of levomethadone hydrochloride having not more than 10 ppm dextromethadone.

Jubanines F-J, cyclopeptide alkaloids from the roots of Ziziphus jujuba

Kang, Kyo Bin,Ming, Gao,Kim, Geum Jin,Ha, Thi-Kim-Quy,Choi, Hyukjae,Oh, Won Keun,Sung, Sang Hyun

, p. 90 - 95 (2016/03/04)

Five Ib-type cyclopeptide alkaloids, jubanines F-J (1-5), and three known compounds, nummularine B (6), daechuine-S3 (7), and mucronine K (8) were isolated from the roots of Ziziphus jujuba. Their structures were fully characterized by spectroscopic analyses in combination with chemical derivatization. Compounds 1-3, and 6 were evaluated for their antiviral activity against the porcine epidemic diarrhea virus (PEDV). Compounds 2, 3, and 6 showed potent inhibitory effects on PEDV replication.

HEPATITIS C VIRUS INHIBITORS

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Page/Page column 84, (2012/02/15)

The present disclosure relates to compounds, compositions and methods for the treatment of hepatitis C virus (HCV) infection. Also disclosed are pharmaceutical compositions containing such compounds and methods for using these compounds in the treatment of HCV infection.

METABOTROPIC GLUTAMATE RECEPTORS 5 MODULATORS AND METHODS OF USE THEREOF

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Page/Page column 121-122, (2012/12/13)

Compounds that modulate GluR5 activity and methods of using the same are disclosed.

HEPATITIS C VIRUS INHIBITORS

-

Page/Page column 132, (2010/12/26)

This disclosure concerns novel compounds of Formula (I) as defined in the specification and compositions comprising such novel compounds. These compounds are useful antiviral agents, especially in inhibiting the function of the NS5A protein encoded by Hepatitis C virus (HCV). Thus, the disclosure also concerns a method of treating HCV related diseases or conditions by use of these novel compounds or a composition comprising such novel compounds.

Hepatitis C Virus Inhibitors

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Page/Page column 50, (2010/10/19)

This disclosure concerns novel compounds of Formula (I) as defined in the specification and compositions comprising such novel compounds. These compounds are useful antiviral agents, especially in inhibiting the function of the NS5A protein encoded by Hepatitis C virus (HCV). Thus, the disclosure also concerns a method of treating HCV related diseases or conditions by use of these novel compounds or a composition comprising such novel compounds.

HEPATITIS C VIRUS INHIBITORS

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Page/Page column 207, (2010/11/03)

This disclosure concerns novel compounds of Formula (I) as defined in the specification and compositions comprising such novel compounds. These compounds are useful antiviral agents, especially in inhibiting the function of the NS5A protein encoded by Hepatitis C virus (HCV). Thus, the disclosure also concerns a method of treating HCV related diseases or conditions by use of these novel compounds or a composition comprising such novel compounds.

HEPATITIS C VIRUS INHIBITORS

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Page/Page column 93, (2009/01/20)

The present disclosure relates to compounds of the following formula (I) or a pharmaceutically acceptable salt thereof, wherein A and B are each phenyl; D and E are each five-membered aromatic rings containing one, two, or three i hcteroatoms independently selected from nitrogen, oxygen, and sulfur; provided that ', at least one of D and E is other than imidazole; compositions and methods for the treatment of Hepatitis C virus (HCV) inf ection. Also disclosed are pharmaceutical compositions containing such compounds and methods f or using these compounds in the treatment of HCV inf ection.

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