Fmoc-Ida-OH

Names

[ Name ]:
Fmoc-Ida-OH

[Synonym ]:
Glycine,N-(carboxymethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]
N-(9-fluorenylmethoxycarbonyl)-iminodiacetic acid
N-Fmoc-iminodiacetic acid
I04-3777
Fmoc-iminodiacetic acid

Biological Activity

[Description]:

2,2'-((((9H-Fluoren-9-yl)methoxy)carbonyl)azanediyl)diacetic acid is a Glycine (HY-Y0966) derivative[1].

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

[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):1793-1144.

Chemical & Physical Properties

[ Density]:
1.41g/cm3

[ Boiling Point ]:
618.4ºC at 760 mmHg

[ Melting Point ]:
213-217ºC

[ Molecular Formula ]:
C₁₉H₁₇NO₆

[ Molecular Weight ]:
355.34100

[ Flash Point ]:
327.8ºC

[ Exact Mass ]:
355.10600

[ PSA ]:
104.14000

[ LogP ]:
2.40670

[ Vapour Pressure ]:
3.77E-16mmHg at 25°C

[ Index of Refraction ]:
1.635

[ Storage condition ]:
2-8°C

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2922509090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2922509090

[ Summary ]:
2922509090. other amino-alcohol-phenols, amino-acid-phenols and other amino-compounds with oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Structure-activity relationships of 1,3-dialkylxanthine derivatives at rat A3 adenosine receptors.

J. Med. Chem. 37 , 3373, (1994)

1,3-Dialkylxanthine analogues containing carboxylic acid and other charged groups on 8-position substituents were synthesized. These derivatives were examined for affinity in radioligand binding assay...