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ChemicalBook > Product Catalog >Biochemical Engineering >Amino Acids and proteins >Arginine

Arginine

Arginine Structure
CAS No.
7004-12-8
Chemical Name:
Arginine
Synonyms
ARGININE;FMOC-L-ARG(PBF)-OPFP;FMOC-ARGININE(PBF)-OPFP;5-Guanidino-2-aminopentanoic acid;N-ALPHA-FMOC-N'-2,2,4,6,7-PENTAMETHYLDIHYDROBENZOFURAN-5-SULFONYL-L-ARGININE PENTAFLUORPHENYL ESTER;FMOC-N-OMEGA-(2,2,4,6,7-PENTAMETHYLDIHYDROBENZOFURAN-5-SULFONYL)-L-ARGININE PENTAFLUOROPHENYL ESTER;N-ALPHA-FMOC-NG-(2,2,4,6,7-PENTAMETHYLDIHYDROBENZOFURAN-5-SULFONYL)-L-ARGININE PENTAFLUOROPHENYL ESTER
CBNumber:
CB6467166
Molecular Formula:
C40H39F5N4O7S
Molecular Weight:
814.82
MOL File:
7004-12-8.mol
Modify Date:
2023/12/25 10:05:17
Request For Quotation

Arginine Properties

storage temp. -15°C
pka 1.82(at 25℃)
InChI InChI=1S/C6H14N4O2/c7-4(5(11)12)2-1-3-10-6(8)9/h4H,1-3,7H2,(H,11,12)(H4,8,9,10)
InChIKey ODKSFYDXXFIFQN-UHFFFAOYSA-N
SMILES C(C(N)C(=O)O)CCNC(=N)N

Arginine Chemical Properties,Uses,Production

Description

Arginine (abbreviated as Arg or R) is an α-amino acid. It was first isolated in 1886 . The L - form is one of the 20 most common natural amino acids. At the level of molecular genetics, in the structure of the messenger ribonucleic acid mRNA, CGU, CGC, CGA, CGG, AGA, and AGG, are the triplets of nucleotide bases or codons that code for arginine during protein synthesis. In mammals, arginine is classified as a semiessential or conditionally essential amino acid, depending on the developmental stage and health status of the individual. Preterm infants are unable to synthesize or create arginine internally, making the amino acid nutritionally essential for them. There are some conditions that put an increased demand on the body for the synthesis of L-arginine, including surgical or other trauma, sepsis and burns . Arginine was first isolated from a lupin seedling extract in 1886 by the Swiss chemist Ernst Schultze.
In general, most people do not need to take arginine supplements because the body usually produces enough.

Chemical Properties

Prisms from water containing two molecules of H2O, anhydrous plates from alcohol solution. Dehydrates at 105C, decomposes at 244C. Sparingly soluble in alcohol; insoluble in ether.

Physical properties

The amino acid side-chain of arginine consists of a 3-carbon aliphatic straight chain, the distal end of which is capped by a complex guanidinium group.
With a pKa of 12.48, the guanidinium group is positively charged in neutral, acidic and even most basic environments, and thus imparts basic chemical properties to arginine. Because of the conjugation between the double bond and the nitrogen lone pairs, the positive charge is delocalized, enabling the formation of multiple H-bonds.

Uses

arginine is also known as l-arginine. This is an amino acid with antistatic, masking, hair-and skin-conditioning properties.

Definition

An essential amino acid for rats, occurring naturally in the l(+) form. Available as glutamate and hydrochloride.

Biological Functions

Arginine plays an important role in cell division, the healing of wounds, removing ammonia from the body, immune function, and the release of hormones.
The benefits and functions attributed to oral supplementation of L-arginine include:
Precursor for the synthesis of nitric oxide (NO)
Reduces healing time of injuries (particularly bone)
Quickens repair time of damaged tissue
Helps decrease blood pressure in clinical hypertensive subjects.

Arginine Preparation Products And Raw materials

Raw materials

Preparation Products

Arginine Suppliers

Global( 22)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Anant Pharmaceuticals Pvt Ltd +91-8550986868 +91-9485998001 Haryana, India 461 58 Inquiry
SynZeal Research Pvt Ltd +1 226-802-2078 Gujarat, India 6522 58 Inquiry
ORCHID PHARMA LTD +91 - 44 - 2821 1000 New Delhi, India 69 58 Inquiry
Chongqing Zhihe Biopharmaceutical Co., Ltd. +86-18580541567 +86-17782035140 China 301 58 Inquiry
ABCR GmbH & CO. KG 49 721 95061 0 Germany 6846 75 Inquiry
Shaanxi Dideu Medichem Co. Ltd 029-81124267 15229202216 China 10011 58 Inquiry
Cato Research Chemicals Inc. 020-81960175-877 18933936954 China 7738 58 Inquiry
Anyang Hongmeng New Materials Co., Ltd 19588588067 19588588067 China 11485 58 Inquiry
ACS DOBFAR SPA +39 02 906931 Italy 69 58 Inquiry
Ajinomoto Co., Inc +81 3 5250 8111 Japan 19 58 Inquiry
Supplier Advantage
Anant Pharmaceuticals Pvt Ltd 58
SynZeal Research Pvt Ltd 58
ORCHID PHARMA LTD 58
Chongqing Zhihe Biopharmaceutical Co., Ltd. 58
ABCR GmbH & CO. KG 75
Shaanxi Dideu Medichem Co. Ltd 58
Cato Research Chemicals Inc. 58
Anyang Hongmeng New Materials Co., Ltd 58
ACS DOBFAR SPA 58
Ajinomoto Co., Inc 58

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5-Guanidino-2-aminopentanoic acid FMOC-L-ARG(PBF)-OPFP FMOC-ARGININE(PBF)-OPFP FMOC-N-OMEGA-(2,2,4,6,7-PENTAMETHYLDIHYDROBENZOFURAN-5-SULFONYL)-L-ARGININE PENTAFLUOROPHENYL ESTER N-ALPHA-FMOC-N'-2,2,4,6,7-PENTAMETHYLDIHYDROBENZOFURAN-5-SULFONYL-L-ARGININE PENTAFLUORPHENYL ESTER N-ALPHA-FMOC-NG-(2,2,4,6,7-PENTAMETHYLDIHYDROBENZOFURAN-5-SULFONYL)-L-ARGININE PENTAFLUOROPHENYL ESTER ARGININE 7004-12-8 C40H39N4O7F5S Arginine Amino Acid Derivatives Specialty Synthesis Peptide Synthesis Arginine [Arg, R] Arginine