L(+)-Arginine Chemical Properties

Melting point:

222 °C (dec.) (lit.)

alpha 

27.1 º (c=8, 6N HCl)

Boiling point:

305.18°C (rough estimate)

Density 

1.2297 (rough estimate)

FEMA 

3819 | L-ARGININE

refractive index 

27 ° (C=8, 6mol/L HCl)

storage temp. 

2-8°C

solubility 

H₂O: 100 mg/mL

form 

powder

pka

1.82, 8.99, 12.5(at 25℃)

color 

white

PH

10.5-12.0 (25℃, 0.5M in H2O)

PH Range

10.5 - 12

Odor

Faint

Odor Type

bland

optical activity

[α]20/D +27°, c = 8 in 6 M HCl

Water Solubility 

148.7 g/L (20 ºC)

Sensitive 

Air Sensitive

λmax

λ: 260 nm Amax: ≤0.2
λ: 280 nm Amax: ≤0.1

Merck 

14,780

JECFA Number

1438

BRN 

1725413

Stability:

Stable. Incompatible with strong oxidizing agents.

InChIKey

ODKSFYDXXFIFQN-BYPYZUCNSA-N

LogP

-4.20

CAS DataBase Reference

74-79-3(CAS DataBase Reference)

NIST Chemistry Reference

L-Arginine(74-79-3)

EPA Substance Registry System

L-Arginine (74-79-3)

Safety Information

Hazard Codes 

Xn,T

Risk Statements 

36-36/37/38-20/21/22-61

Safety Statements 

24/25-36-26-45-53-39

WGK Germany 

3

RTECS 

CF1934200

F 

10-23

TSCA 

Yes

HazardClass 

IRRITANT

HS Code 

29252000

Hazardous Substances Data

74-79-3(Hazardous Substances Data)

Toxicity

cyt-grh-par 100 mmol/L IJEBA6 24,460,86

MSDS

• Language:English Provider:L(+)-Arginine
• Language:English Provider:ACROS
• Language:English Provider:SigmaAldrich
• Language:English Provider:ALFA

L(+)-Arginine Usage And Synthesis

Indications and Usage

Odorless, slightly bitter. Easily soluble in water (solubility in 0℃ water is 83g/L, solubility in 50℃ water is 400g/L), very slightly soluble in ethanol, insoluble in ether; pI6.0; loses its 2-molecule water crystal when heated to 105℃, darkens in color at 230℃, disintegrates at 244℃; its aqueous solution has maximum absorption at 205nm (1gε3.28).
L-Arginine is an encoding amino acid in protein synthesis and is one of the 8 essential amino acids in the human body. The body needs it for many different functions. Taking L-Arginine supplements can treat certain diseases such as congestive heart failure and cystitis. L-Arginine can also act as seasoning for nutrient supplements and food additives. L-Arginine can undergo a heat reaction with sugar (amino-carbonyl reaction) to obtain a unique fragrance, GB 2760-2001, an approved food spice. As an amino acid drug, L-Arginine can be used as pharmaceutical raw material and is an important ingredient in amino acid infusions and integrated amino acid preparations. It is also a crucial amino acid in maintaining infant growth and maturation.

Mechanisms of Action

L-Arginine can stimulate the human body to release certain chemicals such as insulin and human growth hormone. It can also clear ammonia in the body and promote the healing of wounds. The human body also needs it to produce sarcosine. Decomposing L-Arginine produces nitric oxide, which can expand blood vessels and increase blood flow. L-Arginine is an intermediate metabolite in the orthinine cycle and promotes the conversion of ammonia to urea, thus lowering the blood concentration of ammonia. L-Arginine is also an important part of sperm protein and can promote spermatogenesis and provide energy for sperm movement. Additionally, intravenous arginine can stimulate the pituitary to release growth hormone and can be used to test pituitary functions.

Adverse reactions

Abdominal pain, diarrhea, gout and bloating. There may also be increased severity in herpes breakouts and increased effects of antihypertensive drugs, resulting in a lower blood pressure than expected, which may cause hypertensive patients to experience dizziness and fainting.

Toxicity Level

Moderate

Acute Toxicity

Reference data: abdominal cavity – large rat LD50: 3793 mg/kg.

Flammability Characteristics

Flammable. Burning produces toxic nitrogen oxide smoke.

Handling

Store in ventilated, cool and dry area.

Extinguishers

Dry powder, foam, sand, carbon dioxide, water mist.

Chemical Properties

Arginine is a diaminomonocarboxylic acid. The nonessential amino acid, arginine, is a urea cycle amino acid and a precursor for the neurotransmitter nitric oxide, which plays a role in the regulation of the brain’s system of dilation and constriction of small blood vessels. It is strongly alkaline and its water solutions absorb carbon dioxide from the air (FCC, 1996). Functionality in foods includes, but is not limited to, nutrient and dietary supplement

Chemical Properties

White crystalline powder

Physical properties

Solubility 14.87 (20 ℃) g/100 g H2O, pI 10.76, dissociation constants: pK1 2.01, pK2 9.04 (a-NH2), pK3 12.48 (guanidyl).

Occurrence

Reported present in cheese, chocolate, eggs, meat, nuts and other products.

Uses

L-Arginine is used for heart and blood vessel conditions which includes congestive heart failure (CHF), chest pain, high blood pressure and coronary artery disease. It plays a vital role in the treatment of cardiovascular disease due to it being antiatherogenic, anti-ischemic, antiplatelet and antithrombotic. It acts as a growth stimulant and is involved in the treatment of erectile dysfunction in men. It is an important ingredient of tooth paste which provides effective relief for sensitive teeth.

Uses

Amino acid; nutrient.

Uses

L-Arginine has been used:

• as a Roswell park memorial institute medium (RPMI) media component in the isolation and culture of peripheral blood mononuclear cells (PBMCs)
• as a RPMI media component for tissue culture
• in DMEM medium for the identification and quantification of phosphorylation sites by stable isotope labeling by amino acids in cell culture (SILAC) and LCMS/MS

Definition

ChEBI: An L-alpha-amino acid that is the L-isomer of arginine.

Aroma threshold values

Detection at 100%, faint.

Taste threshold values

Taste characteristics at 1000 ppm: hint of sourness.

General Description

L-Arginine is an amino acid that plays a key role in many physiological processes such as tissue repair and reproduction. It is a key precursor for synthesizing nitric oxide in mammals. Due to these factors, the dietary supplementation with L-arginine may show a range of health benefits.

Biochem/physiol Actions

Substrate of nitric oxide synthase, which is converted to citrulline and nitric oxide (NO). Induces insulin release by a nitric oxide-dependent mechanism.

Side effects

Nausea, abdominal pain and diarrhea
Bloating
Gout
Headache
Allergic response
Airway inflammation or worsening of asthma symptoms

Safety Profile

Mutation data reported. Whenheated to decomposition it emits toxic fumes of NOx.

Synthesis

Enzymatically, arginine is formed in two reactions from citrulline. The first reaction (citrulline + succinate) is catalyzed by the enzyme arginosuccinate synthetase. It is ATP dependent and with the formation of a new C–N bond in the gaunidino group of arginosuccinate, water is removed and ATP is hydrolyzed. The second reaction is catalyzed by arginine synthetase and involves the scission of arginosuccinate with the formation of arginine and fumaric acid.

target

NO | IL Receptor | cGMP

Drug interactions

L-arginine may interact with certain medications, including :
Blood-pressure-lowering medications: enalapril (Vasotec), losartan (Cozaar), amlodipine (Norvasc), furosemide (Lasix), etc.
Erectile dysfunction medications: sildenafil citrate (Viagra), tadalafil (Cialis), etc.
Blood-thinning medications: clopidogrel (Plavix), enoxaparin (Lovenox), heparin, warfarin (Coumadin), etc.
Antidiabetic medications: insulin, pioglitazone (Actos), glipizide (Glucotrol), etc.
Medications that increase blood flow: nitroglycerin (Nitro-Dur, Nitro-Bid, Nitrostat), isosorbide ( Sorbitrate, Imdur, Isordil), etc.
Diuretic medications: amiloride (Midamor), and triamterene (Dyrenium), spironolactone (Aldactone), etc.

Purification Methods

S-Arginine crystallises from H2O as the dihydrate and as plates from EtOH. It also crystallises from 66% EtOH. Its solubility in H2O is 15% at 21o. Its isoelectric point is at pH 10.76. [Greenstein & Winitz The Chemistry of the Amino Acids J. Wiley, Vol 3 p 1841 1961, Beilstein 4 IV 817.]

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