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Purine

CAS No.
120-73-0
Chemical Name:
Purine
Synonyms
9H-PURINE;7H-Purine;1H-Purine;X 128;PURINE;NSC 753;Isopurine;Purine 98%;Purine,99%;beta-Purine
CBNumber:
CB6447322
Molecular Formula:
C5H4N4
Molecular Weight:
120.11
MDL Number:
MFCD00079221
MOL File:
120-73-0.mol
MSDS File:
SDS
Last updated:2026-01-30 16:22:46
Product description Number Pack Size Price
Purine 98% P55805 1g $212
Purine P840288 50mg $50
Purine C6588 100mg $50
Purine >98.0% CS-W008627 1g $65
Purine 95+% 075203 1g $175
More product size

Purine Properties

Melting point 214-217 °C (lit.)
Boiling point 214.09°C (rough estimate)
Density 1.3106 (rough estimate)
refractive index 1.7380 (estimate)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly)
pka 2.3(at 20℃)
form Crystals
color White
Water Solubility 400 g/L (20 ºC)
Merck 7942
BRN 3200
InChI 1S/C5H4N4/c1-4-5(8-2-6-1)9-3-7-4/h1-3H,(H,6,7,8,9)
InChIKey KDCGOANMDULRCW-UHFFFAOYSA-N
SMILES c1ncc2nc[nH]c2n1
CAS DataBase Reference 120-73-0(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII W60KTZ3IZY
NCI Dictionary of Cancer Terms purine
NIST Chemistry Reference 9H-Purine(120-73-0)
EPA Substance Registry System Purine (120-73-0)
UNSPSC Code 12352005
NACRES NA.22

SAFETY

Risk and Safety Statements

PPE Eyeshields, Gloves, type N95 (US)
Safety Statements  22-24/25
WGK Germany  3
RTECS  UO7450000
HS Code  29335995
Storage Class 11 - Combustible Solids
Toxicity LD50 intraperitoneal in rat: 800mg/kg
NFPA 704
0
1 0

Purine price More Price(25)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich P55805 Purine 98% 120-73-0 1g $212 2025-07-31 Buy
TRC P840288 Purine 120-73-0 50mg $50 2021-12-16 Buy
ApexBio Technology C6588 Purine 120-73-0 100mg $50 2021-12-16 Buy
ChemScene CS-W008627 Purine >98.0% 120-73-0 1g $65 2021-12-16 Buy
Matrix Scientific 075203 Purine 95+% 120-73-0 1g $175 2021-12-16 Buy
Product number Packaging Price Buy
P55805 1g $212 Buy
P840288 50mg $50 Buy
C6588 100mg $50 Buy
CS-W008627 1g $65 Buy
075203 1g $175 Buy

Purine Chemical Properties,Uses,Production

Chemical Properties

very slightly yellow to cream crystalline powder

Uses

Organic synthesis, metabolism, and biochemi- cal research. (2) One of a number of basic compounds found in living matter and having a purine-type molecular structure.

Uses

Purine can be used human immunogenic epitopes of H,K, and E human endogenous retroviruses.

Uses

Purine can undergo direct C-H functionalization in the presence of palladium catalyst to form various biologically important products.

Definition

A simple nitrogenous organic molecule with a double ring structure. Members of the purine group include adenine and guanine, which are constituents of the nucleic acids, and certain plant alkaloids, such as caffeine and theobromine.

Definition

purine: An organic nitrogenous base(see formula), sparingly soluble inwater, that gives rise to a group ofbiologically important derivatives,notably adenine and guanine,which occur in nucleotides and nucleicacids (DNA and RNA).

Definition

ChEBI: The 9H-tautomer of purine.

Biosynthesis

Basically, the same pathway is found in all organisms capable of purine biosynthesis de novo. The initial substrate is the highly phosphorylated sugar 5-phosphoribosyl-α-1-pyrophosphate (PRPP). An amino group is transferred from glutamine to PRPP catalyzed by the enzyme glutamine PRPP amidotransferase. After that, it takes four reactions to complete the imidazole ring and an additional five reactions to synthesize the pyrimidine moiety and thereby to complete the purine molecule. In some bacteria (e.g., B. subtilis and Escherichia coli), the third step is also catalyzed by a second enzyme (purT) that uses formate instead of a tetrahydrofolic acid derivative as formyl donor. The sixth step has been found to be a two-step reaction, which in some organisms is catalyzed by a single enzyme. The end product of the de novo purine biosynthetic pathway is IMP. After the formation of IMP, purine synthesis splits into two separate pathways leading to the synthesis of AMP and GMP. The control point for feedback inhibition by purine nucleotides and activation by PRPP is on the activity of the first enzyme of the pathway glutamine PRPP amidotransferase. The branching from IMP is regulated by ATP and GTP to ensure a proper balance between ATP and GTP.

General Description

Purine is a heterocyclic organic compound constituting a pyrimidine ring fused to an imidazole ring.

Purification Methods

It crystallises from toluene or EtOH, and sublimes at 100-150o/0.1mm or 160o/10-4mm. The picrate has m 207-209o after crystallisation from 20volumes of H2O. [Beilstein 26 H 354, 26 III/IV 1736.]

13754-19-3
124-38-9
120-73-0
Synthesis of Purine from 4,5-Diaminopyrimidine and Carbon dioxide
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View Lastest Price from Purine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Purine pictures 2026-01-30 Purine
120-73-0
US $39.00 / mg 99.51% 10g TargetMol Chemicals Inc.
Purine pictures 2025-10-13 Purine
120-73-0
US $3.00-9.00 / KG 0.1KG 99% g-kg-tons, free sample is available ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
Purine pictures 2020-02-11 Purine
120-73-0
US $9.80 / KG 1g >98% 20 tons Career Henan Chemical Co
  • Purine pictures
  • Purine
    120-73-0
  • US $39.00 / mg
  • 99.51%
  • TargetMol Chemicals Inc.
  • Purine pictures
  • Purine
    120-73-0
  • US $3.00-9.00 / KG
  • 99%
  • ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
  • Purine pictures
  • Purine
    120-73-0
  • US $9.80 / KG
  • >98%
  • Career Henan Chemical Co
1H-Purine 3,5,7-Triazaindole 6H-Imidazo[4,5-d]pyrimidine 7H-Purine beta-Purine Imidazo(4,5-d)pyrimidine Isopurine NSC 753 X 128 PURINE TIMTEC-BB SBB004288 7H-IMIDAZO[4,5-D]PYRIMIDINE 9H-PURINE Purine,>98% 1H-Purine (9CI) imidazolopyrimidine 3H-imidazo[4,5-d]pyrimidine Purine free base Purine 98% FINE ORGANIC COMPOUND PURINE DERIVATIVE Purine,99% Purine, 99% 1GR Purine Solution Purine USP/EP/BP Purine (6CI, 8CI) Purine, 10 mM in DMSO 120-73-0 BioChemical Biochemicals and Reagents Building Blocks Nucleosides, Nucleotides, Oligonucleotides Purines Heterocyclic Building Blocks Nucleosides PYRIMIDINE Nucleic acids Heterocycles series Purine