Name: Adenosine triphosphate
SKU: 56-65-5

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Basic Information

Molecular Structure:
CAS No.:	56-65-5
Name:	Adenosine triphosphate

Formula:	C₁₀H₁₆N₅O₁₃P₃
Molecular Weight:	507.184
Synonyms:	5'-ATP;ATP;ATP(nucleotide);Adenosine 5'-triphosphate;Adenosine 5'-triphosphoric acid;Adenosine triphosphate;Adenosine, 5'-(tetrahydrogen triphosphate);Adenylpyrophosphoric acid;Adephos;Adetol;Adynol;Atipi;Atriphos;Cardenosine;Fosfobion;Glucobasin;Myotriphos;Phosphobion;Striadyne;Triadenyl;Triphosphaden;Triphosphoric acid adenosine ester;
EINECS:	200-283-2
Density:	2.636 g/cm³
Melting Point:	187 - 190oC (Decomposes)
Boiling Point:	951.429 °C at 760 mmHg
Flash Point:	529.205 °C
Appearance:	white crystalline powder
Safety:	22-24/25
PSA:	308.56000
LogP:	-1.04780

Synthetic route

: 58-64-0
adenosine 5'-diphosphate

A: 35094-46-3
adenosine-5'-O-(3-thiotriphosphate)

B: 56-65-5
ATP

C phosphate: phosphate

Conditions

Conditions	Yield
With dihydroxyacetone phosphate; ethylenediaminetetraacetic acid; DL-dithiothreitol; NAD; trisodium thiophosphate; 2-oxo-propionic acid; magnesium chloride; phosphoglycerate kinase; immobil. triosephosphate isomerase; glyceraldehyde-3-phosphate dehydrogenase; lactate dehydrogenase In water for 72h; Ambient temperature; 1) pH 7.5;	A 80% B n/a C n/a

...Expand

: 5135-30-8
5'-tosyladenosine

: 56-65-5
ATP

Conditions

Conditions	Yield
With tetrakis(tetra-n-butylammonium) hydrogen triphosphate In acetonitrile for 48h; Ambient temperature;	72%

: 61-19-8
5'-adenosine monophosphate

A: 58-64-0
adenosine 5'-diphosphate

B: 56-65-5
ATP

C: 1062-98-2
adenosine 5'-tetraphosphate

Conditions

Conditions	Yield
With manganese(ll) chloride; tri-1-benzimidazolylphosphine oxide at 50℃; for 72h; N-ethylmorpholine buffer (pH 7.0);	A 65% B 17% C 3%
With magnesium chloride; tri-1-benzimidazolylphosphine oxide at 50℃; for 72h; N-ethylmorpholine buffer (pH 7.0);	A 26% B 36% C 18%

...Expand

: 29220-54-0
adenosine 5'-<α-thio>triphosphate

: 56-65-5
ATP

Conditions

Conditions	Yield
With dihydrogen peroxide	65%

: 93978-77-9
tetrakis(tetra-n-butylammonium) hydrogen triphosphate

: 5135-30-8
5'-tosyladenosine

: 56-65-5
ATP

Conditions

Conditions	Yield
In acetonitrile for 23h;	55%

: 61-19-8
5'-adenosine monophosphate

A: 58-64-0
adenosine 5'-diphosphate

B: 56-65-5
ATP

Conditions

Conditions	Yield
With phosphorotriimidazolide; magnesium chloride at 22℃; for 168h; N-ethylmorpholine buffer (pH 7.0);	A 25% B 43%
With 2,3,6-trimethyl-beta-cyclodextrin In water at 37℃; Product distribution; equilibrium constant phosphate buffer, pH 7.00;
With magnesium; β‐cyclodextrin In water at 37℃; Product distribution; equilibrium constant phosphate buffer, pH 7.00;

: Morpholin-4-yl-phosphonic acid mono-{(3aR,4R,6R,6aR)-2-methoxy-6-[6-(4-methoxy-phenylamino)-purin-9-yl]-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl} ester

: 56-65-5
ATP

Conditions

Conditions	Yield
With bis(tri-n-butylammonium) pyrophosphate In N,N-dimethyl-formamide	42%

: 488-69-7
fructose-1,6-bisphosphate

: 61-19-8
5'-adenosine monophosphate

: 56-65-5
ATP

Conditions

Conditions	Yield
With yeast-maceration juice

: 67-07-2
Phosphocreatine

: 61-19-8
5'-adenosine monophosphate

: 56-65-5
ATP

Conditions

Conditions	Yield
With creatine-kinase beim Behandeln mit einem Enzym-Praeparat aus Escherichia coli;

: 61-19-8
5'-adenosine monophosphate

: 56-65-5
ATP

Conditions

Conditions	Yield
With Tri-n-octylamine; phosphoric acid; cyclopentanone-[O-(4-nitro-benzenesulfonyl)-oxime ]; N,N-dimethyl-formamide
With pyridine; phosphoric acid; water; dicyclohexyl-carbodiimide Reagens 4: Tributylamin;
With 5-phosphoribosyl 1-pyrophosphate synthetase; 5-phosphoribosyl 1-pyrophosphate Enzyme kinetics;

Raw Materials

488-69-7

138-08-9

58-61-7

Downstream Products

482-67-7

138-08-9

65-47-4

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Chemistry

Molecular Formula: C₁₀H₁₆N₅O₁₃P₃
Molar mass: 507.181 g/mol
EINECS: 200-283-2
Density: 2.63 g/cm₃
Flash Point: 529.2 °C
Index of Refraction: 1.904
Boiling Point: 951.4 °C at 760 mmHg
Vapour Pressure: 0 mmHg at 25°C
Storage temp: -20°C
Form: Lyophilized powder
Product categories of Adenosine triphosphate (56-65-5): Pharmaceutical Intermediate;Nucleic acid
Structure of Adenosine triphosphate (56-65-5):

XLogP3-AA: -5.7
H-Bond Donor: 7
H-Bond Acceptor: 17
Systematic Name: [5-(6-Aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl (hydroxy-phosphonooxy-phosphoryl) hydrogen phosphate
SMILES: O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
InChI: InChI=1/C10H16N5O13P3/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(26-10)1-25-30(21,22)28-31(23,24)27-29(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H,23,24)(H2,11,12,13)(H2,18,19,20)
InChIKey: ZKHQWZAMYRWXGA-UHFFFAOYAM
Std. InChI: InChI=1S/C10H16N5O13P3/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(26-10)1-25-30(21,22)28-31(23,24)27-29(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H,23,24)(H2,11,12,13)(H2,18,19,20)
Std. InChIKey: ZKHQWZAMYRWXGA-UHFFFAOYSA-N

Uses

Adenosine triphosphate (56-65-5) can be used for pharmaceutical intermediate.

Toxicity Data With Reference

1.	dni-hmn:lym 10 µmol/L	CNREA8 Cancer Research. 42 (1982),2092.
2.	oms-hmn:oth 10 µmol/L	JIDEAE Journal of Investigative Dermatology. 65 (1975),52.
3.	dni-mus:leu 2 µmol/L	CHTHBK Chemotherapy. 27 (1981),61.
4.	ipr-rat LD50:200 mg/kg	BJANAD British Journal of Anesthesia. 53 (1981),305.
5.	ipr-mus LD50:2780 mg/kg	PCJOAU Pharmaceutical Chemistry Journal (English Translation). Translation of KHFZAN. 20 (1986),160.

Consensus Reports

EPA Genetic Toxicology Program. Reported in EPA TSCA Inventory.

Safety Profile

Poison by intraperitoneal route. Human mutation data reported. When heated to decomposition it emits toxic fumes of PO_x and NO_x.

Safety Statements:
22: Do not breathe dust
24: Avoid contact with skin
25: Avoid contact with eyes

Specification

Adenosine triphosphate (56-65-5) also can be called Atriphos ; Striadyne ; Glucobasin ; Triadenyl ; 9-[5-O-(Hydroxy{[hydroxy(phosphonooxy)phosphoryl]oxy}phosphoryl)pentofuranosyl]-9H-purin-6-amine .

56-65-5

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Chemistry

Uses

Toxicity Data With Reference

Consensus Reports

Safety Profile

Specification