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HomeProduct name listL(+)-Arginine

L(+)-Arginine

Synonym(s):L-Arginine;ARG;(S)-2-Amino-5-guanidinopentanoic acid;Abelson murine leukemia viral oncogene homolog 2;Abelson tyrosine-protein kinase 2

  • CAS NO.:74-79-3
  • Empirical Formula: C6H14N4O2
  • Molecular Weight: 174.2
  • MDL number: MFCD00002635
  • EINECS: 200-811-1
  • SAFETY DATA SHEET (SDS)
  • Update Date: 2024-05-10 16:01:40
L(+)-Arginine Structural Picture

What is L(+)-Arginine?

Description

L-Glutamine and?L-arginine are classified as semi-essential or conditionally essential amino acids, which means that the human body can synthesize them under some health conditions but not others. Both are abundant in many foods.
Neither?D-glutamine nor?D-arginine is common in nature, so the?L-amino acids are usually referred to without prefixes. In 1883, German chemists Ernst. Schulze and E. Bosshard isolated?L-glutamine from the juice of sugarbeets. It is the most common amino acid in human blood and a key component of proteins.
In 1886, Schulze was also the first to isolate?L-arginine, in this case from lupin seedlings. It is also an important amino acid in protein biosynthesis.
It turns out that a difference in occurrence between these two amino acids makes a huge difference in huge animals. This year, while examining the melanocortin system* of cetaceans, Roger D. Cone at the University of Michigan (Ann Arbor) and colleagues discovered that the?two suborders of the sea mammals have different components at position 156 in the melanocortin-4 receptor. Glutamine is at this position in baleen whales, whereas toothed whales and dolphins contain arginine instead.
Cone’s group found that arginine in the receptor suppresses the beasts’ appetites relative to the glutamine-containing receptor. They believe that this difference contributes to the much larger sizes of baleen whales.
*The melanocortin system is an important regulator of metabolism, food intake, and fat storage.

Description

L-Glutamine and?L-arginine are classified as semi-essential or conditionally essential amino acids, which means that the human body can synthesize them under some health conditions but not others. Both are abundant in many foods.
Neither?D-glutamine nor?D-arginine is common in nature, so the?L-amino acids are usually referred to without prefixes. In 1883, German chemists Ernst. Schulze and E. Bosshard isolated?L-glutamine from the juice of sugarbeets. It is the most common amino acid in human blood and a key component of proteins.
In 1886, Schulze was also the first to isolate?L-arginine, in this case from lupin seedlings. It is also an important amino acid in protein biosynthesis.
It turns out that a difference in occurrence between these two amino acids makes a huge difference in huge animals. This year, while examining the melanocortin system* of cetaceans, Roger D. Cone at the University of Michigan (Ann Arbor) and colleagues discovered that the?two suborders of the sea mammals have different components at position 156 in the melanocortin-4 receptor. Glutamine is at this position in baleen whales, whereas toothed whales and dolphins contain arginine instead.
Cone’s group found that arginine in the receptor suppresses the beasts’ appetites relative to the glutamine-containing receptor. They believe that this difference contributes to the much larger sizes of baleen whales.
*The melanocortin system is an important regulator of metabolism, food intake, and fat storage.

The Uses of L(+)-Arginine

Amino acid; nutrient.

What are the applications of Application

L-Arginine is a precursor of nitric oxide synthesis that induces vasodilation

Metabolism

Not Available

Properties of L(+)-Arginine

Melting point: 222 °C (dec.) (lit.)
Boiling point: 305.18°C (rough estimate)
Density  1.2297 (rough estimate)
storage temp.  2-8°C
solubility  H2O: 100 mg/mL
form  powder
appearance white crystals or powder
appearance white crystals or powder
color  white
Water Solubility  148.7 g/L (20 ºC)
Sensitive  Air Sensitive

Safety information for L(+)-Arginine

Signal word Warning
Pictogram(s)

Exclamation Mark
Irritant
GHS07
GHS Hazard Statements H319:Serious eye damage/eye irritation
Precautionary Statement Codes P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P337+P313:IF eye irritation persists: Get medical advice/attention.
P403:Store in a well-ventilated place.

Computed Descriptors for L(+)-Arginine

InChIKey ODKSFYDXXFIFQN-BYPYZUCNSA-N

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