2-Amino-4-hydroxy-1H-pteridine
2-Amino-4-hydroxy-1H-pteridine Basic information
- Product Name:
- 2-Amino-4-hydroxy-1H-pteridine
- Synonyms:
-
- 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
- CAS:
- 2236-60-4
- MF:
- C6H5N5O
- MW:
- 163.14
- EINECS:
- 218-799-1
- Product Categories:
-
- Heterocycles
- Mol File:
- 2236-60-4.mol
2-Amino-4-hydroxy-1H-pteridine Chemical 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℃)
- form
- powder
- biological source
- synthetic
- Water Solubility
- 17.54mg/L(22.5 ºC)
- BRN
- 150294
- InChIKey
- HNXQXTQTPAJEJL-UHFFFAOYSA-N
- CAS DataBase Reference
- 2236-60-4(CAS DataBase Reference)
- NIST Chemistry Reference
- 4(1H)-pteridinone, 2-amino-(2236-60-4)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36-37/39
- WGK Germany
- 3
- RTECS
- UO3505000
- F
- 10-23
- HS Code
- 29335990
MSDS
- Language:English Provider:2-Amino-4-hydroxy-1H-pteridine
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
2-Amino-4-hydroxy-1H-pteridine Usage And Synthesis
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.
Biological Activity
Pterine consists of pyrazine and pyrimidine with substitutions in keto and amino group. Pterine is present in all organisms including cyanobacteria. It acts as a cofactor for redox enzymes and serves as a precursor for folic acid synthesis. Pterine from the butterfly wings absorb light and elicit incoherent scattering. Pterine induces alterations in DNA by hydroxylation of deoxyguanosine.
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
Preparation Products
Raw materials
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2-Amino-4-hydroxy-1H-pteridine(2236-60-4)Related Product Information
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- EC 2.6.1.2
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- 3-Aminophenol
- ALTRENOGEST
- Glycine
- Triamterene
- 6-Aminocaproic acid
- Tris(hydroxymethyl)aminomethane
- 10-Formylfolic Acid
- 2-Amino-4-hydroxypteridine-6-methanol
- 2-Amino-7-(chloromethyl)pteridin-4(1H)-one
- Levomefolate calcium
- N-(p-Aminobenzoyl)glutamic acid
- Folic Acid Impurity C
- (2S)-2-[[4-[Bis[(2-aMino-4-oxo-1,4-dihydropteridin-6-yl)Methyl]aMino]benzoyl]aMino]pentanedioic Acid