ChemicalBook >> CAS DataBase List >>2,4-DIAMINO-6-(HYDROXYMETHYL)PTERIDINE

2,4-DIAMINO-6-(HYDROXYMETHYL)PTERIDINE

CAS No.
945-24-4
Chemical Name:
2,4-DIAMINO-6-(HYDROXYMETHYL)PTERIDINE
Synonyms
Methotrexate EP Impurity A;AKOS 213-118;Methotrexate-EP-Imp-A;Methotrexate IMpurity A;Pralatrexate Impurity 3;Methotrexate Impurity 1(EP-A);2,4-Diaminopteridine-6-methanol;2,4-DIAMINO-6-PTERIDINEMETHANOL;2,4-diaminopteridine-6-ylmethanol;6-pteridinemethanol, 2,4-diamino-
CBNumber:
CB4364405
Molecular Formula:
C7H8N6O
Molecular Weight:
192.18
MDL Number:
MFCD00006711
MOL File:
945-24-4.mol
MSDS File:
SDS
Last updated:2026-01-13 11:21:12
Product description Number Pack Size Price
2,4-Diamino-6-(hydroxymethyl)pteridine 95% 861634 25mg $82.5
2,4-Pteridinediamine-6-methanol P840095 25mg $65
2,4-Pteridinediamine-6-methanol P840095 250mg $155
2,4-Diamino-6-(hydroxymethyl)pteridine 3136AH 25g $370
(2,4-Diaminopteridin-6-yl)methanol CS-B0318 1g $104
More product size

2,4-DIAMINO-6-(HYDROXYMETHYL)PTERIDINE Properties

Melting point 333-334 °C (decomp)
Boiling point 560.2±60.0 °C(Predicted)
Density 1.673±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility DMSO (Slightly), Methanol (Slightly, Heated)
pka 12.00±0.10(Predicted)
form Solid
color Light Brown to Dark Yellow
InChI InChI=1S/C7H8N6O/c8-5-4-6(13-7(9)12-5)10-1-3(2-14)11-4/h1,14H,2H2,(H4,8,9,10,12,13)
InChIKey CYNARAWTVHQHDI-UHFFFAOYSA-N
SMILES N1=C2C(N=C(CO)C=N2)=C(N)N=C1N
CAS DataBase Reference 945-24-4(CAS DataBase Reference)
FDA UNII 1RU16O4RO0
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P280-P305+P351+P338
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xn
Risk Statements  22
WGK Germany  3
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral

2,4-DIAMINO-6-(HYDROXYMETHYL)PTERIDINE price More Price(14)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 861634 2,4-Diamino-6-(hydroxymethyl)pteridine 95% 945-24-4 25mg $82.5 2026-03-19 Buy
TRC P840095 2,4-Pteridinediamine-6-methanol 945-24-4 25mg $65 2021-12-16 Buy
TRC P840095 2,4-Pteridinediamine-6-methanol 945-24-4 250mg $155 2021-12-16 Buy
AK Scientific 3136AH 2,4-Diamino-6-(hydroxymethyl)pteridine 945-24-4 25g $370 2021-12-16 Buy
ChemScene CS-B0318 (2,4-Diaminopteridin-6-yl)methanol 945-24-4 1g $104 2021-12-16 Buy
Product number Packaging Price Buy
861634 25mg $82.5 Buy
P840095 25mg $65 Buy
P840095 250mg $155 Buy
3136AH 25g $370 Buy
CS-B0318 1g $104 Buy

2,4-DIAMINO-6-(HYDROXYMETHYL)PTERIDINE Chemical Properties,Uses,Production

Chemical Properties

Orange-Yellow Solid

Uses

2,4-Pteridinediamine-6-methanol (Methotrexate EP Impurity A) is an impurity of Methotrexate. A useful reagent for the development of selective antiparasitic compounds.

Synthesis

1,3-Dihydroxyacetone

96-26-4

Pyrimidinetetramine sulfate

5392-28-9

2,4-DIAMINO-6-(HYDROXYMETHYL)PTERIDINE

945-24-4

1. Barium chloride (7.32 g, 30 mmol) was added rapidly to an aqueous suspension of tetraaminopyrimidine sulfate (7.14 g, 30 mmol). The reaction mixture was heated at 100 °C for 10 min and then cooled to room temperature. The resulting barium sulfate solid was removed by filtration. 2. The above filtrate was transferred to a 1 L three-necked round-bottomed flask fitted with a mechanical stirrer pre-filled with 450 mL of an aqueous 4 M sodium acetate solution containing dihydroxyacetone (8 g, 90 mmol) and cysteine hydrochloride monohydrate (3.63 g, 30 mmol). The reaction mixture was stirred at room temperature, open to air for 24 hours. 3. Upon completion of the reaction, the precipitated yellow solid was collected by filtration, washed sequentially with water and ethanol, and subsequently dried in a heated vacuum oven overnight to afford 3.4 g (66% yield) of the crude product 2,4-diamino-6-hydroxymethylpteridine. 4. Purification of the crude product: the yellow solid was dissolved in 10% acetic acid and a few drops of concentrated hydrochloric acid were added. The solution was heated to 75°C, treated with the addition of activated carbon and subsequently thermally filtered. 5. Neutralize the filtrate with ammonia to neutral and precipitate a bright yellow solid. The solid was collected by filtration, washed sequentially with water, water-ethanol mixture and ethanol, and finally dried overnight in a heated vacuum oven to give 2.8 g (54% yield) of purified 2,4-diamino-6-hydroxymethylpteridine.

References

[1] Patent: WO2010/110907, 2010, A1. Location in patent: Page/Page column 48-49

73978-41-3
945-24-4
Synthesis of 2,4-DIAMINO-6-(HYDROXYMETHYL)PTERIDINE from (2,4-DIAMINOPTERIDIN-6-YL)METHANOL HYDROCHLORIDE HYDRATE
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View Lastest Price from 2,4-DIAMINO-6-(HYDROXYMETHYL)PTERIDINE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2,4-DIAMINO-6-(HYDROXYMETHYL)PTERIDINE pictures 2025-12-12 2,4-DIAMINO-6-(HYDROXYMETHYL)PTERIDINE
945-24-4
US $1.00-0.00 / KG 1KG 99% 10000KG Shaanxi Dideu Medichem Co. Ltd
2,4-PteridinediaMine-6-Methanol  pictures 2020-02-26 2,4-PteridinediaMine-6-Methanol
945-24-4
US $1.00-1.00 / KG 1KG 99%+ 100 tons Shaanxi Dideu Medichem Co. Ltd
2,4-Pteridinediamine-6-Methanol  pictures 2020-02-26 2,4-Pteridinediamine-6-Methanol
945-24-4
US $0.00-0.00 / Kg 1KG 99.0%+ 100 tons Shaanxi Dideu Medichem Co. Ltd
AKOS 213-118 (2,4-DIAMINO-PTERIDIN-6-YL)-METHANOL (2,4-DIAMINO-6-PTERIDINYL)METHANOL 2,4-DIAMINO-6-PTERIDINEMETHANOL 2,4-DIAMINO-6-(HYDROXYMETHYL)PTERIDINE 2,4-diaminopteridine-6-ylmethanol 2,4-Diamino-6-hydroxymethylpteridine hydrochloride or HBR 2,4-DIAMINO-6-HYDROXYMETHYLPTERIDINE, 95 % 2,4-Diaminopteridine-6-methanol Methotrexate-EP-Imp-A 2,4-Diamino-6-(hydroxymethyl)pteridine 95% 6-pteridinemethanol, 2,4-diamino- Methotrexate EP Impurity A Methotrexate Impurity 1(EP-A) Methotrexate IMpurity A Pralatrexate Impurity 3 Methotrexate Impurity 1(Methotrexate EP Impurity A) 2, 4-diamino-6-hydroxymethylterenidine 945-24-4 Quinazolines Heterocyclic Building Blocks Building Blocks Benzhydrols, Benzyl & Special Alcohols Heterocycles Aromatics Compounds Aromatics Bases & Related Reagents Inhibitors Nucleotides