ChemicalBook Product Catalog Chemical Reagents Organic reagents fatty acid N-ME-AIB-OH HCL

N-ME-AIB-OH HCL

N-ME-AIB-OH HCL Basic information
Product Name:N-ME-AIB-OH HCL
Synonyms: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
CAS:2566-34-9
MF:C5H11NO2
MW:117.15
EINECS:219-898-2
Product Categories:
Mol File:2566-34-9.mol
N-ME-AIB-OH HCL Structure
N-ME-AIB-OH HCL Chemical 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
pka2.17±0.10(Predicted)
form powder to crystal
color White to Almost white
BRN 1746984
Safety Information
Hazard Codes Xi
Risk Statements 36
Safety Statements 26
WGK Germany 3
HS Code 2922.49.8000
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
N-ME-AIB-OH HCL Usage And Synthesis
Chemical PropertiesWHITE CRYSTALLINE POWDER
DefinitionChEBI: 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acid is a non-proteinogenic alpha-amino acid that is isobutyric acid in which the alpha-hydrogen has been replaced by a methylamino group.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
N-ME-AIB-OH HCL Preparation Products And Raw materials
Raw materialsMethylamine hydrochloride-->POTASSIUM CYANIDE-->Methylamine-->Acetone-->2-Bromo-2-methylpropionic acid
Preparation Products2-Methyl-2-methylamino-propionamide
4-Anilino-1-benzyl-4-piperidinecarboxylic acid FMOC-ACPC-OH METHYL 1,5-DIBENZYL-4,6-DIOXO-3-PHENYLOCTAHYDROPYRROLO[3,4-C]PYRROLE-1-CARBOXYLATE METHYL 3-(2-CHLOROPHENYL)-5-(4-CHLOROPHENYL)-4,6-DIOXO-1-PHENYLOCTAHYDROPYRROLO[3,4-C]PYRROLE-1-CARBOXYLATE Fmoc-Aib-OH METHYL 1,5-DIBENZYL-3-(2-CHLOROPHENYL)-4,6-DIOXOOCTAHYDROPYRROLO[3,4-C]PYRROLE-1-CARBOXYLATE A,A-DIPHENYL-4-MORPHOLINEACETIC ACID, SODIUM SALT METHYL 1-BENZYL-3-(4-METHOXYPHENYL)-4,6-DIOXO-5-PHENYLOCTAHYDROPYRROLO[3,4-C]PYRROLE-1-CARBOXYLATE 2-[[(2,6-DIMETHOXYPYRIMIDIN-4-YL)CARBONYL]AMINO]-2-METHYLPROPANOIC ACID, METHYL ESTER METHYLAMINOBUTYRIC ACID, ALPHA-, [1-14C] N-ME-AIB-OH HCL 1-BOC-3-AMINOPIPERIDINE FMOC-AIB-OPFP METHYLAMINOISOBUTYRIC ACID, [N-METHYL-3H] METHYL 1-BENZYL-5-(4-CHLOROPHENYL)-3-(4-METHOXYPHENYL)-4,6-DIOXOOCTAHYDROPYRROLO[3,4-C]PYRROLE-1-CARBOXYLATE METHYL 3,5-BIS(4-CHLOROPHENYL)-4,6-DIOXO-1-PHENYLOCTAHYDROPYRROLO[3,4-C]PYRROLE-1-CARBOXYLATE METHYL 1-BENZYL-3-(4-METHOXYPHENYL)-4,6-DIOXO-5-[3-(TRIFLUOROMETHYL)PHENYL]OCTAHYDROPYRROLO[3,4-C]PYRROLE-1-CARBOXYLATE METHYL 1,5-DIBENZYL-3-(4-CHLOROPHENYL)-4,6-DIOXOOCTAHYDROPYRROLO[3,4-C]PYRROLE-1-CARBOXYLATE
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