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FMOC-HIS-OH

FMOC-HIS-OH Structure
CAS No.
116611-64-4
Chemical Name:
FMOC-HIS-OH
Synonyms
Fmoc-His;FMOC-HIS-OH;Fmoc-L-His-OH;FMOC-HISTIDINE;FMOC-L-HISTIDINE;Nα-Fmoc-L-histidine;N-a-Fmoc-L-histidine;N-α-Fmoc-L-histidine;FMOC-HIS-OH USP/EP/BP;Nα-Fmoc-L-histidine99%
CBNumber:
CB8687841
Molecular Formula:
C21H19N3O4
Molecular Weight:
377.39
MOL File:
116611-64-4.mol
Modify Date:
2024/7/3 10:46:41

FMOC-HIS-OH Properties

Melting point 171-174 °C(Solv: methanol (67-56-1); water (7732-18-5))
Boiling point 706.7±60.0 °C(Predicted)
Density 1.372±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,2-8°C
solubility DMSO (Slightly), DMF (Slightly, Sonicated), Methanol (Very Slightly, Heated)
pka 3.26±0.10(Predicted)
form Solid
color White
InChIKey SIRPVCUJLVXZPW-IBGZPJMESA-N
SMILES C(O)(=O)[C@H](CC1N=CNC=1)NC(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
HS Code  29332900

FMOC-HIS-OH price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
SRL 17849 FMOC-L-Histidine extrapure, 98% 116611-64-4 5Gms ₹3860 2022-05-26 Buy
Product number Packaging Price Buy
17849 5Gms ₹3860 Buy

FMOC-HIS-OH Chemical Properties,Uses,Production

Description

Nα-Fmoc-L-histidine (FMOC-HIS-OH) holds great significance as a synthetic amino acid extensively employed in peptide synthesis. Its versatility makes it a highly sought-after reagent, widely used in various synthetic processes to create peptides, proteins, and even small molecules. Moreover, it catalyzes peptide and protein synthesis, further enhancing its utility. It is pivotal in unravelling biological processes such as enzymatic catalysis, protein structure, and drug design. Notably, this remarkable amino acid aids in understanding cell signalling pathways, which bear paramount importance in comprehending the mechanisms underlying diseases. The mechanism of action for Nα-Fmoc-L-histidine revolves around its ability to form essential peptide bonds. These bonds arise through a reaction with specific reagents, like DCC, leading to the creation of peptides. Subsequently, deprotection of the peptide bond occurs with the addition of a base, such as sodium hydroxide, followed by an acid, like trifluoroacetic acid.

Uses

Nα-Fmoc-L-histidine is an N-Fmoc-protected form of L-Histidine (H456010). L-Histidine is an essential amino acid that plays an important role in mitochondrial glutamine transport and has potential of abolishing oxidative stress caused by brain edema.L-Histidine promotes zinc uptake in human erythrocyes and also has potential as an antioxidant therapy for acute mammary inflammation in cattle.

FMOC-HIS-OH Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 122)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
Sisco Research Laboratories Pvt. Ltd. +91-22-4268 5800 Mumbai, India 4317 58 Inquiry
Triveni chemicals 08048762458 New Delhi, India 6093 58 Inquiry
Sichuan HongRi Pharma-Tech Co.,Ltd +86-028-64841719 +8617390183901 China 1358 58 Inquiry
Capot Chemical Co.,Ltd. 571-85586718 +8613336195806 China 29798 60 Inquiry
ATK CHEMICAL COMPANY LIMITED +undefined-21-51877795 China 32760 60 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29901 58 Inquiry
Chongqing Chemdad Co., Ltd +86-023-6139-8061 +86-86-13650506873 China 39916 58 Inquiry
CONIER CHEM AND PHARMA LIMITED +8618523575427 China 49391 58 Inquiry
Career Henan Chemica Co +86-0371-86658258 +8613203830695 China 30253 58 Inquiry
FMOC-L-HISTIDINE FMOC-HIS-OH FMOC-HISTIDINE N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-HISTIDINE N-α-Fmoc-L-histidine N-a-Fmoc-L-histidine N-.ALPHA.-FMOC -L-HISTIDINE Fmoc-L-His-OH Nα-(9H-Fluorene-9-ylmethoxycarbonyl)-L-histidine (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(1H-imidazol-4-yl)propanoic acid Fmoc-His N-[(9H-Fluoren-9-ylMethoxy)carbonyl]-L-histidine Nα-Fmoc-L-histidine99% (((9H-Fluoren-9-yl)methoxy)carbonyl)-L-histidine (9H-Fluoren-9-yl)MethOxy]Carbonyl His-OH (2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-(1H-imidazol-5-yl)propanoic acid N^a-Fmoc-L-histidine,98% (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(1H-imidazol-5-yl)propanoicaci FMOC-HIS-OH USP/EP/BP Nα-Fmoc-L-histidine FMOC-L-Histidine extrapure, 98% (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1H-imidazol-4-yl)propanoic acid|||(((9H-Fluoren-9-yl)methoxy)carbonyl)-L-histidine|||FMOC-L-Histidine 116611-64-4 3116611-64-4