Fmoc-D-Ile-OH Chemical Properties

Melting point:

143-145°C

Boiling point:

559.8±33.0 °C(Predicted)

Density 

1?+-.0.06 g/cm3(Predicted)

storage temp. 

Sealed in dry,2-8°C

solubility 

Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.

form 

Powder

pka

3.92±0.22(Predicted)

color 

White to off-white

optical activity

Consistent with structure

InChI

InChI=1S/C21H23NO4/c1-3-13(2)19(20(23)24)22-21(25)26-12-18-16-10-6-4-8-14(16)15-9-5-7-11-17(15)18/h4-11,13,18-19H,3,12H2,1-2H3,(H,22,25)(H,23,24)/t13-,19-/m1/s1

InChIKey

QXVFEIPAZSXRGM-BFUOFWGJSA-N

SMILES

C(O)(=O)[C@@H]([C@H](C)CC)NC(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O

CAS DataBase Reference

143688-83-9(CAS DataBase Reference)

Safety Information

WGK Germany 

3

F 

10

HS Code 

2924 29 70

MSDS

• Language:English Provider:SigmaAldrich

Fmoc-D-Ile-OH Usage And Synthesis

Chemical Properties

White solid

Uses

N-Fmoc-D-isoleucine is the N-Fmoc-protected form of D-Isoleucine (I820210). D-Isoleucine is not biosynthesized in the human body and is therefore categorized as an essential amino acid that must be obtained through diet. It is also an important building block that is used in the formation of hemoglobin in humans.

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

Fmoc-D-Ile-OH(143688-83-9)Related Product Information

• 1,1'-Carbonyldiimidazole
• (2R,3R)-2-Amino-3-methylpentanoic acid
• CARBONYL SULFIDE
• Folic acid
• Stearic acid
• Hyaluronic acid
• METHOXYCARBONYLSULFENYL CHLORIDE
• Fmoc-N'-methyltrityl-L-lysine
• L-Isoleucine
• Fmoc-8-amino-3,6-dioxaoctanoic acid
• DL-Isoleucine
• L-Leucine
• N-CARBOBENZOXY-DL-LEUCINE
• 9-Fluorenylmethyl chloroformate
• Ethyl 2-(Chlorosulfonyl)acetate
• Citric acid
• Fmoc-OSu
• Fmoc-D-glutamic acid gamma-tert-butyl ester