ChemicalBook > CAS DataBase List > Fmoc-Aib-OH

Fmoc-Aib-OH

Product Name
Fmoc-Aib-OH
CAS No.
94744-50-0
Chemical Name
Fmoc-Aib-OH
Synonyms
FMoc-Aib;FMOC-(ME)ALA-OH;FMOC-AIB-OH;FMOC-ARB-OH;FMoc-a-Me-Ala-OH;BOC-3-IODO-ALA-OME;RARECHEM EM WB 0053;Fmoc--methylalanine;FMOC-ALPHA-ME-ALA-OH;Fmoc-Aib-OH USP/EP/BP
CBNumber
CB3495317
Molecular Formula
C19H19NO4
Formula Weight
325.36
MOL File
94744-50-0.mol
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Fmoc-Aib-OH Property

Melting point:
182-188 °C
Boiling point:
544.3±33.0 °C(Predicted)
Density 
1.256±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
pka
3.98±0.10(Predicted)
form 
powder to crystal
color 
White to Almost white
Sensitive 
Moisture Sensitive
BRN 
5604328
InChIKey
HOZZVEPRYYCBTO-UHFFFAOYSA-N
CAS DataBase Reference
94744-50-0(CAS DataBase Reference)
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Safety

Safety Statements 
22-24/25
WGK Germany 
3
F 
10-21
HazardClass 
IRRITANT
HS Code 
29242990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P321Specific treatment (see … on this label).

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P362Take off contaminated clothing and wash before reuse.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
8.52049
Product name
Fmoc-Aib-OH
Purity
Novabiochem?
Packaging
1g
Price
$39.9
Updated
2024/03/01
Sigma-Aldrich
Product number
8.52049
Product name
Fmoc-Aib-OH
Purity
Novabiochem?
Packaging
5G
Price
$164
Updated
2024/03/01
Sigma-Aldrich
Product number
8.52049
Product name
Fmoc-Aib-OH
Purity
Novabiochem?
Packaging
25g
Price
$649
Updated
2024/03/01
Sigma-Aldrich
Product number
47691
Product name
Fmoc-α-Me-Ala-OH
Purity
≥97.0% (HPLC)
Packaging
5g
Price
$57.24
Updated
2024/03/01
TCI Chemical
Product number
F0888
Product name
2-[(9H-Fluoren-9-ylmethoxy)carbonylamino]isobutyric Acid
Purity
>98.0%(HPLC)(T)
Packaging
5g
Price
$86
Updated
2024/03/01
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Fmoc-Aib-OH Chemical Properties,Usage,Production

Chemical Properties

Fmoc-Aib-OH is beige powder

Uses

L-Fmoc-Aminobutyric Acid, is an alanine derivative used in chemical synthesis and peptide chemistry.

Uses

Fmoc-Aib-OH is used for studying receptor-ligand interactions using encoded amino acid scanning.

Fmoc-Aib-OH Preparation Products And Raw materials

Raw materials

Preparation Products

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Fmoc-Aib-OH Suppliers

Americas 1 Canada 1 China 207 Europe 1 France 1 Germany 6 Hungary 1 India 5 Japan 4 Switzerland 4 United Kingdom 4 United States 26 Global 261
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View Lastest Price from Fmoc-Aib-OH manufacturers

Sichuan HongRi Pharma-Tech Co.,Ltd
Product
Fmoc-Aib-OH 94744-50-0
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
1T
Release date
2023-11-16
Sichuan Jiaying Lai Technology Co.,LTD
Product
Fmoc-Aib-OH 94744-50-0
Price
US $1.00/g
Min. Order
1g
Purity
98%
Supply Ability
100KG
Release date
2019-07-23
Career Henan Chemical Co
Product
Fmoc-Aib-OH 94744-50-0
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
20kg
Release date
2018-08-15

94744-50-0, Fmoc-Aib-OHRelated Search:

Sucrose acetate isobutyrate Paraquat dichloride Diethylstilbestrol α-Lipoic Acid Basic Violet 1 Propionic acid OCTYL ISOBUTYRATE Isobutyric acid N-(9-Fluorenylmethoxycarbonyloxy)succinimide Methanol Kresoxim-methyl Methyl acrylate DL-3-Aminoisobutyric acid 9-Fluorenylmethyl chloroformate Methyl 2-bromo-2-methylpropionate Acetonitrile 2-Aminoisobutyric Acid Methyl acetate

  • N-[(9H-fluoren-9-ylmethoxy)carbonyl]-α-aminoisobutyric acid
  • N-FMOC-C-ALPHA-METHYLALANINE
  • N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-ALPHA-METHYL-L-ALANINE
  • N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-ALPHA-AMINOISOBUTYRIC ACID
  • N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-AMINOISOBUTYRIC ACID
  • N-ALPHA-FMOC-ALPHA-AMINOISOBUTYRIC ACID
  • N-ALPHA-FMOC-L-ALPHA-AMINOISOBUTYRIC ACID
  • FMoc-2-aMinoisobutyric acid FMoc-α-Methylalanine
  • 2-[(9H-Fluoren-9-ylMethoxy)carbonylaMino]isobutyric Acid
  • 2-(FMoc-aMino)isobutyric acid, 98%
  • Fmoc-2-Amino-2-methylpropionic acid
  • Alanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-2-methyl-
  • Fmoc-α-aminoisobutyric acid≥ 99% (HPLC)
  • Fmoc-Aib-OH Novabiochem
  • (9H-Fluoren-9-yl)MethOxy]Carbonyl Aib-OH
  • N-Fmoc-2-methyl-DL-alanine
  • RARECHEM EM WB 0053
  • FMOC-AIB-OH
  • FMOC-2-AMINOISOBUTYRIC ACID
  • FMOC-ALPHA-ME-ALA-OH
  • FMOC-ALPHA-AMINOISOBUTYRIC ACID
  • FMOC-ALPHA-METHYLALANINE
  • FMOC-(ME)ALA-OH
  • 2-(9h-fluoren-9-ylmethoxycarbonylamino)-2-methyl-propanoic acid
  • N-Fmoc-2-aminoisobutyric acid
  • fmoc-α-aminoisobutyric acid
  • N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-ISOBUTYRIC ACID, FMOC-ALPHA-METHYL-ALANINE
  • BOC-3-IODO-ALA-OME
  • N- α -Fmoc- α -aminoisobutyricacid
  • NALPHA-9-Fluorenylmethoxycarbonyl-2-aminoisobutyric acid
  • Fmoc--methylalanine
  • 2-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]-2-(methyl-d3)propionic Acid
  • Fmoc-(methyl-d3)alanine
  • N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-(methyl-d3)alanine
  • N-9-Fluorenylmethoxycarbonyl-α-aminoisobutyric Acid-d3
  • N-9-Fluorenylmethoxycarbonyl-a-aminoisobutyric Acid-d3
  • Fmoc-α-aminoisobutyric acid, Fmoc-α-methylalanine
  • FMoc-Aib-OH(FMoc-α-aMinoisobutyric acid)
  • FMoc-Aib
  • FMoc-a-Me-Ala-OH
  • FMOC-ARB-OH
  • 2-[(9H-Fluoren-9-ylmethoxy)carbonylamino]isobutyricAcid&gt
  • 2-(9H-fluoren-9-ylmethoxycarbonylamino)-2-methylpropanoicaci
  • N-Fmoc-alpha-methylalanine
  • Fmoc-Aib-OH USP/EP/BP
  • Fmoc-α-aminoisobutyric acid
  • N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-methylalanine
  • 2-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]-2-methylpropionic acid
  • Fmoc-a-aminoisobutyric acid,97%
  • N-Fmoc-α-aminoisobutyric acid
  • 94744-50-0
  • 744-50-0
  • 94744-54-0
  • C19H16D3NO4
  • Alanine Derivatives
  • Peptide Synthesis
  • Unnatural Amino Acid Derivatives
  • Specialty Synthesis