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2-Amino-4-hydroxy-1H-pteridine

CAS No.
2236-60-4
Chemical Name:
2-Amino-4-hydroxy-1H-pteridine
Synonyms
PTERIN;PTERINE;4-oxopterin;pteridoxamine;Pterine, ≥98%;Pterin【keto form】;2-Amino-4-oxodihyd;2-AMINO-4-PTERIDINOL;2-Aminopteridin-4-ol;Folic Acid Impurity 34
CBNumber:
CB3140406
Molecular Formula:
C6H5N5O
Molecular Weight:
163.14
MDL Number:
MFCD00010557
MOL File:
2236-60-4.mol
MSDS File:
SDS
Last updated:2023-05-04 17:34:36

2-Amino-4-hydroxy-1H-pteridine Properties

Melting point 300 °C
Boiling point 290.2°C (rough estimate)
Density 1.4240 (rough estimate)
refractive index 1.9000 (estimate)
storage temp. Keep in dark place,Inert atmosphere,2-8°C
pka 2.27(at 20℃)
Water Solubility 17.54mg/L(22.5 ºC)
BRN 150294
InChIKey HNXQXTQTPAJEJL-UHFFFAOYSA-N
CAS DataBase Reference 2236-60-4(CAS DataBase Reference)
FDA UNII 85MA24E1NH
NIST Chemistry Reference 4(1H)-pteridinone, 2-amino-(2236-60-4)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-37/39
WGK Germany  3
RTECS  UO3505000
10-23
HS Code  29335990
NFPA 704
0
1 0

2-Amino-4-hydroxy-1H-pteridine price More Price(22)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich P1132 Pterine ~95% 2236-60-4 50mg $92.5 2024-03-01 Buy
Sigma-Aldrich P1132 Pterine ~95% 2236-60-4 1g $292.8 2024-03-01 Buy
Sigma-Aldrich P1132 Pterine ~95% 2236-60-4 250mg $158 2024-03-01 Buy
TRC P839870 Pterin 2236-60-4 1g $185 2021-12-16 Buy
Biosynth Carbosynth FA12181 2-Amino-4-hydroxypteridine 2236-60-4 500mg $120 2021-12-16 Buy
Product number Packaging Price Buy
P1132 50mg $92.5 Buy
P1132 1g $292.8 Buy
P1132 250mg $158 Buy
P839870 1g $185 Buy
FA12181 500mg $120 Buy

2-Amino-4-hydroxy-1H-pteridine Chemical Properties,Uses,Production

Chemical Properties

YELLOW-BEIGE CRYSTALLINE POWDER

Uses

Pterin is used in the biosynthesis and metabolism of tetrahydrobiopterin and molybdopterin.

Definition

ChEBI: 2-aminopteridin-4-ol is a 2-amino-4-hydroxypteridine. It is a tautomer of a 2-aminopteridin-4(3H)-one and a 2-aminopteridin-4(1H)-one.

Purification Methods

It is dissolved in hot 1% aqueous ammonia, filtered, and an equal volume of hot 1M aqueous formic acid is added. The solution is allowed to cool at 0-2o overnight. The solid is collected and washed with distilled water several times by centrifugation and dried in vacuo over P2O5 overnight, and then at 100o overnight (any ammonium formate in the sample evaporates off). [Beilstein 26 III/IV 3936.]

2-Amino-4-hydroxy-1H-pteridine Preparation Products And Raw materials

Global( 109)Suppliers
Supplier Tel Email Country ProdList Advantage
Capot Chemical Co.,Ltd.
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Changzhou Ansciep Chemical Co., Ltd.
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Alchem Pharmtech,Inc.
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CONIER CHEM AND PHARMA LIMITED
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Career Henan Chemica Co
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Aromsyn Co., Ltd.
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Hebei Weibang Biotechnology Co., Ltd
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Aceschem Inc.
+1-817863-6948 +1-(817)863-6948 sales@aceschem.com United States 19632 58
LEAPCHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 43340 58
2-AMino-1,5-dihydropteridin-4-ol 2-AMINO-4-OXODIHYDROPTERIDINE 2-AMINO-4-PTERIDINOL 2-AMINO-4-HYDROXYPTERIDINE 2-AMINO-4-HYDROXY-1H-PTERIDINE PTERIN PTERINE 2-amino-1H-pteridin-4-one 2-Amino-4-oxy-3,4-dihydropteridine 2-amino-4-hydroxyaminopteridine 4(1H)-Pteridinone,2-amino- 2-amino-4(1h)-pteridinon 2-amino-4(1h)-pteridinone 4-oxopterin pteridoxamine 2-AMINO-4-HYDROXYPTERIDINE 98% 2-Amino-4-hydroxypteridine, 2-Amino-4-oxodihydropteridine 2-Aminopteridin-4(1H)-one 2-Aminopteridin-4-ol Pterin【keto form】 2-Amino-4-hydroxy-1H-pteridine,97% 2-Amino-4-hydroxy-1H-pteridinePterin 2-Amino-4-hydroxypteridine ,97% 2-Amino-4-oxodihyd 2-Aminopteridin-4(3H)-one 2-Amino-3H-pteridin-4-one Sapropterin Dihydrochloride Impurity D 4(3H)-Pteridinone, 2-amino- Folic Acid Impurity 34 Pterine, ≥98% 2-aminopteridin-4(8H)-one Sepiapterin Impurity 9 2236-60-4 C6H5N5O Biochemicals and Reagents BioChemical Enzyme Inhibitors by Type Enzymes, Inhibitors, and Substrates Enzyme Inhibitors Cofactors Substrate Analogs Oxidation-Reduction Heterocycles