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N-ME-AIB-OH HCL

CAS No.
2566-34-9
Chemical Name:
N-ME-AIB-OH HCL
Synonyms
MeAIB;H-MEAIB-OH;N-ME-AIB-OH;H-N-Me-Aib-OH;H-(ME)MEALA-OH;N-ME-AIB-OH HCL;N-Me-a-Me-Ala-OH;2,N-DIMETHYLALANINE;N,2-DIMETHYLALANINE;Methylamino Hydrate
CBNumber:
CB6316473
Molecular Formula:
C5H11NO2
Molecular Weight:
117.15
MDL Number:
MFCD00004191
MOL File:
2566-34-9.mol
MSDS File:
SDS
Last updated:2023-06-08 17:06:38

N-ME-AIB-OH HCL Properties

Melting point 300 °C
Boiling point 192.5±23.0 °C(Predicted)
Density 1.2000 (estimate)
refractive index 1.4650 (estimate)
storage temp. Keep in dark place,Sealed in dry,Store in freezer, under -20°C
Water Solubility almost transparency in Water
form powder to crystal
pka 2.17±0.10(Predicted)
color White to Almost white
BRN 1746984
FDA UNII 26F96C8MBJ

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H319
Precautionary statements  P305+P351+P338
Hazard Codes  Xi
Risk Statements  36
Safety Statements  26
WGK Germany  3
HS Code  2922.49.8000
NFPA 704
0
2 0

N-ME-AIB-OH HCL price More Price(20)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich M2383 α-(Methylamino)isobutyric acid ≥97% (titration) 2566-34-9 250mg $53.2 2024-03-01 Buy
Sigma-Aldrich M2383 α-(Methylamino)isobutyric acid ≥97% (titration) 2566-34-9 1g $152 2024-03-01 Buy
TCI Chemical M1388 2-(Methylamino)isobutyric Acid Hydrate >98.0%(T) 2566-34-9 1g $65 2024-03-01 Buy
TCI Chemical M1388 2-(Methylamino)isobutyric Acid Hydrate >98.0%(T) 2566-34-9 5g $192 2024-03-01 Buy
Usbiological 459276 N-Me-Aib-OH HCl 2566-34-9 100mg $305 2021-12-16 Buy
Product number Packaging Price Buy
M2383 250mg $53.2 Buy
M2383 1g $152 Buy
M1388 1g $65 Buy
M1388 5g $192 Buy
459276 100mg $305 Buy

N-ME-AIB-OH HCL Chemical Properties,Uses,Production

Chemical Properties

WHITE CRYSTALLINE POWDER

Definition

ChEBI: Alpha-(methylamino)isobutyric acid is a non-proteinogenic alpha-amino acid that is isobutyric acid in which the alpha-hydrogen has been replaced by a methylamino group. It has a role as a human urinary metabolite. It is an alanine derivative, a non-proteinogenic alpha-amino acid and a secondary amino compound. It is functionally related to an isobutyric acid. It is a conjugate acid of a N-methyl-aminoisobutyrate zwitterion.

Synthesis Reference(s)

The Journal of Organic Chemistry, 60, p. 8120, 1995 DOI: 10.1021/jo00130a002

2052-01-9
74-89-5
2566-34-9
Synthesis of N-ME-AIB-OH HCL from 2-Bromo-2-methylpropionic acid and Methylamine

N-ME-AIB-OH HCL Preparation Products And Raw materials

N-ME-AIB-OH HCL Suppliers

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N-ME-ALPHA-AMINOISOBUTYRIC ACID N-ME-ALPHA-ME-ALA-OH N-ME-AIB-OH N-ME-AIB-OH HCL N-METHYL-ALPHA-AMINOISOBUTYRIC ACID N-METHYL-ALPHA-AMINOISOBUTYRIC ACID HYDROCHLORIDE N-METHYL-ALPHA-METHYL-ALANINE N-METHYL-ALPHA-METHYLALANINE HYDROCHLORIDE N,2-DIMETHYLALANINE 2,N-DIMETHYLALANINE 2-(METHYLAMINO)ISOBUTYRIC ACID 2-(METHYLAMINO)-2-METHYLPROPIONIC ACID ALPHA-(METHYLAMINO)ISOBUTYRIC ACID H-(ME)MEALA-OH H-MEAIB-OH A-(METHYLAMINO)ISOBUTYRIC ACID N-Methyl-a-aminoisobutyric acid 2-(METHYLAMINO)ISOBUTYRIC ACID HYDRATE 2-Methyl-2-(methylamino)propionic acid MeAIB Methylaminoisobutanoic acid 2-(Methylamino)isobutyric acid,99% α-(Methylamino)isobutyric acid,2,N-Dimethylalanine, 2-(Methylamino)-2-methylpropionic acid N-Me-a-Me-Ala-OH N-METHYL-A-AMINOISOBUTYRIC ACID HYDROCHLORIDE 2-Methyl-2-(MethylaMino)propanoic acid hydrate N-Methyl-α-aminoisobutyric acid hydrochloride 2-(Methylamino)isobutyric Acid  N,2-Dimethyl-DL-alanine 2-Methyl-2-(methylamino) N-Methyl-α-aminoisobutyric acid hydrochloride≥ 98% (TLC) N-Methyl-α-methylalanine hydrochloride 2,N-Dimethylalanine, 2-(Methylamino)-2-methylpropionic acid 2-Methyl-2-(methylamino)propanoic acid 2-(Methylamino)isobutyricAcidHydrate> Methylamino Hydrate Alanine, N,2-dimethyl- 2-methyl-2-(methylamino)propanoicaci H-N-Me-Aib-OH α-(Methylamino)isobutyric acid N-Methyl-α-aminoisobutyric acid hydrochloride 2566-34-9 CH3NHCCH32COOH C5H11NO2xH2O Biochemicals and Reagents Amino Acids and Peptides BioChemical Modified Amino Acids I - Z Peptide Synthesis N-Methyl Amino Acids Specialty Synthesis Unnatural Amino Acid Derivatives