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Arginine

Arginine Struktur
7004-12-8
CAS-Nr.
7004-12-8
Englisch Name:
Arginine
Synonyma:
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
Summenformel:
C40H39F5N4O7S
Molgewicht:
814.82
MOL-Datei:
7004-12-8.mol

Arginine Eigenschaften

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

Sicherheit

Arginine Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

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.

Chemische Eigenschaften

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.

Physikalische Eigenschaften

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.

Verwenden

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.

Biologische Funktion

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 Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Arginine Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 21)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Chongqing Zhihe Biopharmaceutical Co., Ltd.
+86-18580541567; +8618580541567
sales@zhswyy.com China 301 58
GL Biochem (Shanghai) Ltd 21-61263452 13641803416
ymbetter@glbiochem.com China 9981 64
Xibao Biotechnology (Shanghai) Co., Ltd. 13761246140
58642714@qq.com China 415 58
Nanjing Shizhou Biology Technology Co.,Ltd 13675144456
sean.lv@synzest.com China 10784 58
Shaanxi Dideu Medichem Co. Ltd 029-61856358 15229202216
1020@dideu.com China 10011 58
Cato Research Chemicals Inc. 020-81960175-877 18933936954
tianwen.zhan@cato-chem.com China 7735 58

7004-12-8()Verwandte Suche:


  • 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
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