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L-Histidinamide, also known as L-histidine amide, is a chemical compound derived from the amino acid L-histidine. It is formed by the removal of the carboxyl group (-COOH) from the side chain of L-histidine and the subsequent addition of an amide group (-CONH2). L-Histidinamide is a white crystalline solid that is soluble in water and has a molecular formula of C6H10N4O. It plays a significant role in various biological processes, including enzyme catalysis and protein structure stabilization, due to its unique imidazole ring, which can participate in hydrogen bonding and metal ion chelation. L -HISTIDINAMIDE is also used as a building block in the synthesis of pharmaceuticals and other bioactive molecules.

7621-14-9

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7621-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7621-14-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,2 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7621-14:
(6*7)+(5*6)+(4*2)+(3*1)+(2*1)+(1*4)=89
89 % 10 = 9
So 7621-14-9 is a valid CAS Registry Number.

7621-14-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-amino-3-(1H-imidazol-5-yl)propanamide

1.2 Other means of identification

Product number -
Other names L-histidinamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7621-14-9 SDS

7621-14-9Downstream Products

7621-14-9Relevant academic research and scientific papers

HEMIAMINAL-TAG FOR PROTEIN LABELING AND PURIFICATION

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Page/Page column 22; 23, (2018/06/30)

The invention pertains to the synthesis, isolation, and characterization of hemiaminal for selective labeling of peptides, proteins, antibodies, and organic fragments with -C(=0) CH2NH2 and derivatives with -CH2NH2 group over -C(=0) CHRNH2 group (where R≠H). The invention also pertains to the method of single-site immobilization of proteins through N-terminus Gly on solid phase. The invention includes late-stage tagging of N-terminus Gly with an affinity tag, 19F NMR probe, and a fluorophore and a method for metal-free protein purification and isolation of analytically pure proteins.

RENIN INHIBITORS

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, (2008/06/13)

The invention concerns novel renin-inhibitory peptides which are useful for treating renin associated hypertension and for treating hyperaldosteronism. Novel intermediates, processes for preparing both the intermediates and the novel peptides, pharmaceutical compositions, and methods of treatment are included.

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