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Adenosine triphosphate

CAS No.
56-65-5
Chemical Name:
Adenosine triphosphate
Synonyms
ATP-H;ADENOSINE 5'-TRIPHOSPHATE;((2R,3S,4R,5R)-5-(6-Amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate;atipi;5’-atp;adetol;adynol;ATP.H2;adephos;atriphos
CBNumber:
CB0712934
Molecular Formula:
C10H16N5O13P3
Molecular Weight:
507.18
MDL Number:
MFCD00065467
MOL File:
56-65-5.mol
Last updated:2024-04-22 18:05:02

Adenosine triphosphate Properties

Melting point 144°C (rough estimate)
Boiling point 951.4±75.0 °C(Predicted)
alpha D22 -26.7° (c = 3.095)
Density 1.0 g/mL at 20 °C
storage temp. Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
form lyophilized powder
pka pK2: 4.00(-1);pK3: 6.48(-2) (25°C)
Water Solubility Water : ≥ 100 mg/mL (197.17 mM)
InChIKey ZKHQWZAMYRWXGA-KQYNXXCUSA-N
SMILES C(OP(=O)(O)OP(O)(=O)OP(O)(O)=O)[C@H]1O[C@@H](N2C3C(=C(N=CN=3)N)N=C2)[C@H](O)[C@@H]1O
LogP -4.180 (est)
CAS DataBase Reference 56-65-5(CAS DataBase Reference)
EWG's Food Scores 1
NCI Dictionary of Cancer Terms adenosine triphosphate
FDA UNII 8L70Q75FXE
EPA Substance Registry System Adenosine triphosphate (56-65-5)

SAFETY

Risk and Safety Statements

Safety Statements  22-24/25
WGK Germany  3
Toxicity dni-hmn:lym 10 mmol/L CNREA8 42,2092,82

Adenosine triphosphate price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC A281845 Adenosine5''-Triphosphate 56-65-5 5g $60 2021-12-16 Buy
Usbiological 151558 Adenosine Triphosphate 56-65-5 200ul $581 2021-12-16 Buy
Usbiological A0015 Adenosine Triphosphate 56-65-5 100Tests $804 2021-12-16 Buy
ChemScene CS-7674 ATP 98.34% 56-65-5 100mg $60 2021-12-16 Buy
Ark Pharm P000447884 ((2R,3S,4R,5R)-5-(6-Amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate 95+% 56-65-5 100g $144 2021-12-16 Buy
Product number Packaging Price Buy
A281845 5g $60 Buy
151558 200ul $581 Buy
A0015 100Tests $804 Buy
CS-7674 100mg $60 Buy
P000447884 100g $144 Buy

Adenosine triphosphate Chemical Properties,Uses,Production

Description

Adenosine triphosphate, also known as ATP, is a molecule that carries energy within cells. It is one of the most important biological compounds because of its role in supplying energy for life. ATP is the universal energy carrier used by all organisms to supply energy for biological functions. It is often referred to as the energy currency of cells.
ATP also functions as a neurotransmitter that is stored and secreted with other neurotransmitters from the pancreas. ATP is a nucleotide consisting of the nucleoside adenosine with three attached phosphate groups (see Adenine). Like other nucleotides, ATP consists of three parts: a sugar, an amine base, and a phosphate group. The central part of the molecule in ATP is the sugar ribose. The amine base adenine is attached to the ribose, forming adenosine. Opposite the adenine on the ribose is attached a chain of three phosphate groups.

Chemical Properties

The structure of Adenosine triphosphate has an ordered carbon compound as a backbone, but the part that is really critical is the phosphorous part - the triphosphate. Three phosphorous groups are connected by oxygens to each other, and there are also side oxygens connected to the phosphorous atoms. Under the normal conditions in the body, each of these oxygens has a negative charge, and therefore repel each other. These bunched up negative charges want to escape - to get away from each other, so there is a lot of potential energy here.
If you remove just one of these phosphate groups from the end, so that there are just two phosphate groups, the molecule is much happier. This conversion from ATP to ADP is an extremely crucial reaction for the supplying of energy for life processes. Just the cutting of one bond with the accompanying rearrangement is sufficient to liberate about 7.3 kilocalories per mole = 30.6 kJ/mol. This is about the same as the energy in a single peanut.
hyperphysics.phy-astr.gsu.edu

Originator

Atepodin ,Medix ,Spain

History

ATP was first isolated by the German chemist Karl Lohmann (1898–1978) from muscle tissue extracts in 1929. Alexander Todd’s (1907–1997) research helped to clarify ATP’s structure, and it was first synthesized by Todd in 1948.

Uses

Adenosine triphosphate (ATP) plays a critical role in the transport of macromolecules such as proteins and lipids into and out of the cell.  The hydrolysis of ATP provides the required energy for active transport mechanisms to carry such molecules across a concentration gradient.

Synthesis

ATP is synthesized in organisms by several related mechanisms. Oxidative phosphorylation is the main process that aerobic organisms use to produce ATP. Oxidative phosphorylation produces ATP from ADP and inorganic phosphate (Pi) from the oxidation of nicotinamide adenine dinucleotide (NADH) by molecular oxygen in the cell’s mitochondria.
Glycolysis is another process that generates ATP. Glycolysis converts glucose into pyruvate and in the process also forms NADH and ATP. The process can be represented as: Glucose + 2ADP + 2NAD+ + 2Pi → 2 pyruvate + 2ATP + 2NADH + 2H+. In this reaction Pi represents free inorganic phosphate. The rate of glycolysis in the body is inversely related to the amount of available ATP. Pyruvate produced by glycolysis can enter the Krebs cycle, producing more ATP.

Definition

Adenosine triphosphate (ATP) is the source of energy for use and storage at the cellular level. It is an adenosine 5'-phosphate in which the 5'-phosphate is a triphosphate group. It is involved in the transportation of chemical energy during metabolic pathways.

Manufacturing Process

With a solution of 0.29 part by weight of well dried 1,3- dicyclohexylguanidinium adenosine 5'-phosphoramidate in 5 parts by volume of ortho-chlorophenol is admixed a solution of 0.95 part by weight of bistriethylammonium pyrophosphate in a mixed solvent composed of 1 part by volume of ortho-chlorophenol and 2 parts by volume of acetonitrile. The mixture is left standing at 20°C for 2 days. Then 30 parts by volume of water is added to the mixture. After washing with three 15 parts by weight volumeportions of diethyl ether, the aqueous layer is separated, and the remaining diethyl ether in the aqueous layer is removed under reduced pressure. Five parts by weight of activated charcoal is added to the aqueous layer and the mixture is stirred for 30 minutes. The activated charcoal is filtered and further 1 part by weight of activated charcoal is added to the filtrate. After 20 minutes agitation, the activated charcoal is taken out by filtration. The combined activated charcoal is washed with a little water, and eluted twice with respective 300 and 200 parts by volume-portions of 50% (volume) ethanol containing 2% (volume) of concentrated aqueous ammonia. The eluate is concentrated to 40 parts by volume, then is passed through a column packed with 20 parts by volume of a strongly basic anion exchange resin in bead form (chloric type) (polystyrene trimethylbenzyl ammonium type resin sold under the name of Dowex-1 from Dow Chemical Company, Mich. USA). Then, the column is washed with 750 parts by volume of an acid aqueous saline solution containing 0.01 normal hydrochloric acid and 0.02 normal sodium chloride and then eluted with 600 parts by volume of an acid aqueous saline solution composed of 0.01 normal hydrochloric acid and 0.2 normal sodium chloride. After neutralizing with a diluted sodium hydroxide solution, the eluate is treated with activated charcoal to adsorb ATP as its sodium salt. The separated activated charcoal is washed with water and eluted with 60% (volume) ethanol containing 2% (volume) of concentrated aqueous ammonia. The eluate is concentrated to 0.5 part by volume, then 5 parts by volume of ethanol is added. The precipitate thus deposited is centrifuged and dried at low temperature to obtain 0.155 part by weight of tetra-sodium salt of ATP containing 4 mols of water of crystallization as a colorless crystalline powder. The yield is 47% relative to the theoretical.

Therapeutic Function

Coenzyme, Vasodilator

Agricultural Uses

Adenosine triphosphate (ATP) is a nucleotide of fundamental importance as a carrier of chemical energy in all living organisms. The most important function of phosphorus in a plant system is to store and transfer energy. During biochemical processes, ATP gets synthesized to store releasable energy with the breakdown of ATP to adenosine triphosphate (ADP) and to phosphate ion by dephosphorylation. Here, ADP and ATP act as energy currency within the plant.

Safety Profile

Poison by intraperitoneal route.Human mutation data reported. When heated todecomposition it emits toxic fumes of POx and NOx.

Purification Methods

ATP is purified by precipitating it as the barium salt on adding excess barium acetate solution to a 5% solution of ATP in water. The precipitate is filtered off, washed with distilled water, dissolved in 0.2M HNO3 and again precipitated with barium acetate. The precipitate, after several washings with distilled water, is redissolved in 0.2M HNO3, and slightly more than an equivalent of 0.2M H2SO4 is added to precipitate all the barium as BaSO4 which is filtered off. The ATP is then precipitated by addition of a large excess of 95% ethanol. It is filtered off, washed several times with 100% EtOH and finally with dry diethyl ether. It is dried in vacuo. [Kashiwagi & Rabinovitch J Phys Chem 59 498 1955, Beilstein 26 III/IV 3654.]

857447-44-0
56-65-5
Synthesis of Adenosine triphosphate from Adenosine, 5'-O-(2-sulfido-1,3,2-oxathiaphospholan-2-yl)-, 2',3'-diacetate
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Adenosine triphosphate pictures 2024-04-22 Adenosine triphosphate
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Adenosine triphosphate Spectrum

Adenosine 5'-triphosphate, sodium salt solution glucobasin myotriphos striadyne triadenyl triphosaden triphosphaden ADENOSINE-5'- TRIPHOSPHORIC ACID ADENOSINE-5'-TRIPHOSPHATE, IMMOBILIZED ON AGAROSE 4B ADENOSINE TRIPHOSPHATE 5'-ATP-AGAROSE 4B 5’-atp 9-beta-d-arabinofuranosyladenine5’-triphosphate adenosine5’-(tetrahydrogentriphosphate) adenylpyrophosphoricacid adephos adetol adynol atipi atp(nucleotide) atriphos ADENOSINE-5?TRIPHOSPHORIC ACID (ATP) pure Adenphos Striphos ADENOSINE TRIPHOSPHATE, DISODIUM SALT (ATP) 5'-Adenyldiphosphoric acid Adenosine-5 [[[(2S,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl]oxy-hydroxy-phosphoryl]oxyphosphonic acid Adenosine-5''-triphosphoric acid (and/or unspecified salts) [(2R,3S,4R,5R)-5-(6-Aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl (hydroxy-phosphonooxyphosphoryl) hydrogen phosphate 5'-Deoxyadenylate triphosphate Adenosini triphosphas Adenosine triphospha ATP.H2 2’-Deoxyadenosine 5’-Triphosphate(dATP) Cardenosine Triphosphoric acid adenosine ester Adenosine Triphosphate Disdium Salt(Atp) ATP, 200mM sodium salt solution ATP, 325mM solution Adenosine 5-triphosphate (ATP) Disodium Salt Adenosine 5-triphosphate (ATP) Disodium Salt (USP grade) ATP .Free Acid Adenosine triphosphate USP/EP/BP Adenosine triphosphate hydrate ATP-,5'-ATP abs60159 Adenosine triphosphate, Adenosine 5’-triphosphate,ATP Adenosin-5'-triphosphat ATP-H ((2R,3S,4R,5R)-5-(6-Amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate ADENOSINE 5'-TRIPHOSPHATE ATP, 100mM Sodium Solution Adenosine 5'-triphosphate;Adenosine 5'-(tetrahydrogen triphosphate);Adenosine triphosphate;Adenosine-5'-triphosphoric acid;ATP;5'-ATP;Adenylpyrophosphoric acid;Adenphos;Adetol;Atipi;Atriphos;Striadyne;Striphos;Triadenyl;Triphosaden Adenosine triphosphate (ATF) ATP 100mM Sodium Solution, GMP grade ATP 200mM Tris Solution, GMP grade ATP 200mM Tris Solution