Aminophylline CAS#317-34-0

  • CAS Number: 317‑34‑0

  • Chemical Formula: C₉H₁₆N₆O₂

  • Synonyms: Aminophylline (Phyllocontin, Truphylline), Anhydrous Theophylline‑Ethylenediamine Complex, Theophylline compound with ethylenediamine

  • Appearance: Fine, free‑flowing white powder

  • Product Introduction: Anhydrous aminophylline is a coordination complex formed by theophylline and ethylenediamine. It serves as an important pharmaceutical raw material intermediate, widely used for related respiratory‑targeted formulation manufacturing. Our product maintains stable physical properties and consistent batch‑to‑batch quality for overseas bulk procurement.

  • Package Option: Normally packed in 25 kg net weight drums, suitable for ocean container transportation.

  • Minimum order basis: Full container load (FCL) as the base order quantity. We provide bulk supply shipped in complete sea‑going containers, which helps optimize production scheduling, packaging efficiency and overall logistics cost for international buyers. Small consolidated LCL shipments are not available for this item.

Aminophylline CAS#317‑34‑0

Aminophylline is a medicinal compound blended from the bronchodilator theophylline and ethylenediamine at a 2:1 ratio. Acting as a non‑selective adenosine receptor antagonist, histone deacetylase activator and phosphodiesterase inhibitor, it is primarily applied to treat multiple pulmonary disorders such as asthma, COPD, chronic bronchitis and emphysema. Its pharmacological activity in the human body comes from the theophylline fraction. Theophylline works to relax smooth muscles within bronchial passages and pulmonary blood vessels. It competitively blocks type III and type IV phosphodiesterase (PDE), the enzyme responsible for degrading cyclic AMP inside smooth muscle cells, and this mechanism may bring about bronchodilation. Theophylline also attaches to adenosine A2B receptors to counter adenosine‑triggered bronchial narrowing. In addition, under inflammatory conditions, theophylline is capable of activating histone deacetylase, thereby suppressing the transcription of inflammatory genes that rely on histone acetylation to start transcription processes.

 

Aminophylline Chemical Properties

Melting point 

269-270 °C

storage temp. 

Inert atmosphere,Store in freezer, under -20°C

solubility 

H2O: 3.7 mg/mL solutions should be freshly prepared.

pka

pKa 5.0 (Uncertain)

form 

powder

color 

white to off-white

Water Solubility 

soluble

Merck 

14,465

Cosmetics Ingredients Functions

SKIN CONDITIONING
SURFACTANT - CLEANSING

InChI

InChI=1S/C7H8N4O2.C2H8N2/c1-10-5-4(8-3-9-5)6(12)11(2)7(10)13;3-1-2-4/h3H,1-2H3,(H,8,9);1-4H2

InChIKey

LHRHXWBJUQKYEL-UHFFFAOYSA-N

SMILES

O=C1N(C(=O)N(C)C2NC=NC1=2)C.C(N)CN

LogP

-0.175 (est)

CAS DataBase Reference

317-34-0(CAS DataBase Reference)

EPA Substance Registry System

1H-Purine-2,6-dione, 3,7-dihydro-1,3-dimethyl-, compd. with 1,2-ethanediamine (2:1) (317-34-0)

Safety Information

Hazard Codes 

Xn,C

Risk Statements 

22-42/43-34-36/37/38-20/21/22

Safety Statements 

45-36/37/39-26-23-36

RIDADR 

UN 2811 6.1/PG 3

WGK Germany 

3

RTECS 

XH5600000

10-23

TSCA 

TSCA listed

HazardClass 

6.1(b)

PackingGroup 

III

HS Code 

29339900

Hazardous Substances Data

317-34-0(Hazardous Substances Data)

Toxicity

LD50 orally in mice: 540 mg/kg (Thompson, Warren)

Product Application Of Aminophylline CAS#317‑34‑0

Aminophylline features notable vasodilatory and anti‑inflammatory pharmacological properties, and it is occasionally adopted in clinical practice for the therapeutic management of chronic obstructive pulmonary disorder (COPD). In pre‑clinical animal models built for allergen‑triggered pulmonary inflammation, aminophylline can effectively reduce the concentration of inflammatory mediators including IL‑5 and IL‑8, as well as cut down eosinophil counts to ease lung inflammatory responses. This compound is predominantly processed for the formulation of injectable products, and it is widely applied in the production of intravenous injection solutions for relevant pharmaceutical preparations.

Lead Time

‑ Goods from existing inventory: Shipment can be arranged within 2‑3 working days upon receipt of formal order confirmation.

‑ Newly manufactured batches: Production and preparation will take 7‑10 working days before delivery.

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