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94744-50-0

94744-50-0 structure
94744-50-0 structure

Name 2-(9H-fluoren-9-ylmethoxycarbonylamino)-2-methylpropanoic acid
Synonyms FMOC-ALPHA-ME-ALA-OH
FMOC-A-METHYLALANINE
Fmoc-2-Aminoisobutyric acid
Fmoc-alpha-methylalanine
MFCD00151913
FMOC-ALPHA-METHYL-ALANINE
FMOC-ALPHA-AMINOISOBUTYRIC ACID
Fmoc-2-aminoisobutyricacid
FMOC-A-ME-ALA-OH
2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methylpropanoic acid
FMOC-2-AMINO ISOBUTYRIC ACID
N-Fmoc-2-aminoisobutyric acid
FMOC-AMINOISOBUTYRIC ACID (FMOC-AIB-OH)
Fmoc-Aib-OH
Alanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-2-methyl-
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-methylalanine
L B656 HHJ H1OVMX1&1&VQ
N-Fmoc-aminoisobutyric acid
Description Fmoc-Aib-OH is an alanine derivative[1].
Related Catalog
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1065.

Density 1.3±0.1 g/cm3
Boiling Point 544.3±33.0 °C at 760 mmHg
Melting Point 182-188ºC
Molecular Formula C19H19NO4
Molecular Weight 325.358
Flash Point 283.0±25.4 °C
Exact Mass 325.131409
PSA 75.63000
LogP 3.89
Vapour Pressure 0.0±1.5 mmHg at 25°C
Index of Refraction 1.600
Storage condition 2-8°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924299090
HS Code 2924299090
Summary 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%