Amyl nitrate - 1002-16-0

Amyl nitrate

Catalog Number: EVT-520138
CAS Number: 1002-16-0
Molecular Formula: C5H11NO3
Molecular Weight: 133.15 g/mol
The product is for non-human research only. Not for therapeutic or veterinary use.

Product Introduction

Description

Amyl nitrate, often confused with amyl nitrite, is a compound that has been studied in various contexts due to its potential effects on biological systems. While the provided papers do not directly discuss amyl nitrate, they do provide insight into the effects of related nitrites and nitrates on biological systems, particularly in the context of neurodegenerative diseases and pulmonary function. Amyl nitrite is a vasodilator and has been used in medical treatments, and its action may share similarities with that of amyl nitrates due to the related chemical structure and reactivity with biological molecules1 2.

Mechanism of Action

The mechanism of action of amyl nitrite, which may be extrapolated to amyl nitrates, involves the release of nitric oxide (NO) upon administration. This NO can react with superoxide to form peroxynitrite (ONOO–), a potent oxidizing and nitrating agent. In the context of neurodegenerative diseases, such as Alzheimer's disease, the formation of peroxynitrite can lead to the nitration of tyrosine residues in proteins, which is a pathological event associated with the progression of these diseases1. In the pulmonary system, amyl nitrite has been shown to cause a lowering of pulmonary blood pressure, suggesting a direct vasodilatory action on the pulmonary blood vessels. This supports the existence of a vasodilator mechanism in the lungs, which could be relevant for the treatment of certain lung diseases2.

Applications in Various Fields

Neurodegenerative Diseases

In Alzheimer's disease, increased levels of nitrated proteins have been observed in the brain and cerebrospinal fluid (CSF), implicating reactive nitrogen species (RNS) in the neurodegeneration process. The nitration of proteins can modulate the activity of key enzymes and contribute to the pathophysiology of the disease. Although the specific targets of protein nitration in Alzheimer's disease require further study, the current evidence suggests that nitrates and nitrites may play a significant role in the disease's progression1.

Pulmonary Function

The vasodilatory effects of amyl nitrite on the pulmonary circulation have implications for the treatment of lung diseases. By lowering pulmonary blood pressure, amyl nitrite, and potentially amyl nitrates, could be used to manage conditions where pulmonary hypertension is a concern. The research suggests a revision of the current use of nitrites in treating lung diseases, indicating that these compounds may have broader applications than previously thought2.

Properties

CAS Number

1002-16-0

Product Name

Amyl nitrate

IUPAC Name

pentyl nitrate

Molecular Formula

C5H11NO3

Molecular Weight

133.15 g/mol

InChI

InChI=1S/C5H11NO3/c1-2-3-4-5-9-6(7)8/h2-5H2,1H3

InChI Key

HSNWZBCBUUSSQD-UHFFFAOYSA-N

SMILES

CCCCCO[N+](=O)[O-]

Solubility

0.00 M
In water, 360 mg/L at 25 °C
In water, 0.3%

Synonyms

amyl nitrate
pentyl nitrate

Canonical SMILES

CCCCCO[N+](=O)[O-]

Product FAQ

Q1: How Can I Obtain a Quote for a Product I'm Interested In?
  • To receive a quotation, send us an inquiry about the desired product.
  • The quote will cover pack size options, pricing, and availability details.
  • If applicable, estimated lead times for custom synthesis or sourcing will be provided.
  • Quotations are valid for 30 days, unless specified otherwise.
Q2: What Are the Payment Terms for Ordering Products?
  • New customers generally require full prepayment.
  • NET 30 payment terms can be arranged for customers with established credit.
  • Contact our customer service to set up a credit account for NET 30 terms.
  • We accept purchase orders (POs) from universities, research institutions, and government agencies.
Q3: Which Payment Methods Are Accepted?
  • Preferred methods include bank transfers (ACH/wire) and credit cards.
  • Request a proforma invoice for bank transfer details.
  • For credit card payments, ask sales representatives for a secure payment link.
  • Checks aren't accepted as prepayment, but they can be used for post-payment on NET 30 orders.
Q4: How Do I Place and Confirm an Order?
  • Orders are confirmed upon receiving official order requests.
  • Provide full prepayment or submit purchase orders for credit account customers.
  • Send purchase orders to sales@EVITACHEM.com.
  • A confirmation email with estimated shipping date follows processing.
Q5: What's the Shipping and Delivery Process Like?
  • Our standard shipping partner is FedEx (Standard Overnight, 2Day, FedEx International Priority), unless otherwise agreed.
  • You can use your FedEx account; specify this on the purchase order or inform customer service.
  • Customers are responsible for customs duties and taxes on international shipments.
Q6: How Can I Get Assistance During the Ordering Process?
  • Reach out to our customer service representatives at sales@EVITACHEM.com.
  • For ongoing order updates or questions, continue using the same email.
  • Remember, we're here to help! Feel free to contact us for any queries or further assistance.

Quick Inquiry

 Note: Kindly utilize formal channels such as professional, corporate, academic emails, etc., for inquiries. The use of personal email for inquiries is not advised.