Iotalamic acid
Catalog Number: BT-254399
CAS Number: 2276-90-6
Molecular Formula: C11H9I3N2O4
Molecular Weight: 613.91 g/mol
The product is for non-human research only. Not for therapeutic or veterinary use.
Price:
Product Introduction
Description
Iotalamic acid is a contrast agent used in medical imaging procedures such as X-rays, computed tomography (CT), and magnetic resonance imaging (MRI). It is a water-soluble iodinated compound that enhances the visibility of internal organs and tissues during imaging. Iotalamic acid is also used in environmental and industrial research due to its unique properties.
Properties
CAS Number
2276-90-6
Product Name
Iotalamic acid
IUPAC Name
3-acetamido-2,4,6-triiodo-5-(methylcarbamoyl)benzoic acid
Molecular Formula
C11H9I3N2O4
Molecular Weight
613.91 g/mol
InChI
InChI=1S/C11H9I3N2O4/c1-3(17)16-9-7(13)4(10(18)15-2)6(12)5(8(9)14)11(19)20/h1-2H3,(H,15,18)(H,16,17)(H,19,20)
InChI Key
UXIGWFXRQKWHHA-UHFFFAOYSA-N
SMILES
CC(=O)NC1=C(C(=C(C(=C1I)C(=O)O)I)C(=O)NC)I
Synonyms
Acid, Iotalamic
Acid, Iothalamic
Acid, Methalamic
Angio Conray
Angio-Conray
AngioConray
Conray 420
Iodothalamate
Iotalamic Acid
Iothalamate
Iothalamate, Sodium
Iothalamic Acid
Iothalamic Acid, Calcium (2:1) Salt
Iothalamic Acid, Monosilver (1+) Salt
Iothalamic Acid, Monosodium Salt
Iothalamic Acid, Monosodium Salt, Dimer
Lopamidol
Methalamic Acid
Sodium Iothalamate
Acid, Iothalamic
Acid, Methalamic
Angio Conray
Angio-Conray
AngioConray
Conray 420
Iodothalamate
Iotalamic Acid
Iothalamate
Iothalamate, Sodium
Iothalamic Acid
Iothalamic Acid, Calcium (2:1) Salt
Iothalamic Acid, Monosilver (1+) Salt
Iothalamic Acid, Monosodium Salt
Iothalamic Acid, Monosodium Salt, Dimer
Lopamidol
Methalamic Acid
Sodium Iothalamate
Canonical SMILES
CC(=O)NC1=C(C(=C(C(=C1I)C(=O)O)I)C(=O)NC)I
Method of Synthesis or Extraction
Iotalamic acid is synthesized by reacting 5-amino-2,4,6-triiodoisophthalic acid with iodoacetic acid. The reaction takes place in the presence of a catalyst such as triethylamine. The yield of iotalamic acid is around 70-80%, and the process is relatively efficient. However, the synthesis process requires the use of toxic and hazardous chemicals, which can pose a risk to the environment and human health. Therefore, safety measures must be taken during the synthesis process to minimize the risk of exposure to these chemicals.
Chemical Structure and Biological Activity
Iotalamic acid has a molecular formula of C14H8I3NO4 and a molecular weight of 613.93 g/mol. It is a triiodinated derivative of isophthalic acid and contains three iodine atoms that make it an effective contrast agent. Iotalamic acid works by absorbing X-rays and other forms of radiation, which enhances the contrast between the target tissue and surrounding tissues. It is excreted from the body through the kidneys and does not accumulate in the body.
Biological Effects
Iotalamic acid has been shown to have potential therapeutic effects on cell function and signal transduction. It has been used in the treatment of liver cancer and other types of cancer. However, it can also have toxic effects on the body, especially if used in high doses or for prolonged periods. Some of the potential side effects of iotalamic acid include allergic reactions, kidney damage, and thyroid dysfunction.
Applications
In medical research, iotalamic acid is used in drug development and clinical trials to enhance the visibility of internal organs and tissues during imaging. It is also used in environmental research to study the effects of pollutants on ecosystems and to manage pollution. In industrial research, iotalamic acid is used in manufacturing processes to improve product quality and efficiency. However, health and safety considerations must be taken into account when using iotalamic acid in industrial settings.
Future Perspectives and Challenges
Despite its widespread use, iotalamic acid has some limitations in terms of its application and study. For example, it can cause adverse reactions in some patients, and its long-term effects on the body are not well understood. Therefore, more research is needed to fully understand the potential benefits and risks of iotalamic acid. Additionally, new and improved contrast agents are being developed that may offer better performance and fewer side effects.
Conclusion:
Iotalamic acid is a widely used contrast agent in medical imaging, environmental research, and industrial applications. Its unique properties make it an effective tool for enhancing the visibility of internal organs and tissues during imaging. However, its use must be carefully monitored to minimize the risk of adverse reactions and environmental damage. Further research is needed to fully understand the potential benefits and risks of iotalamic acid and to develop new and improved contrast agents.
Conclusion:
Iotalamic acid is a widely used contrast agent in medical imaging, environmental research, and industrial applications. Its unique properties make it an effective tool for enhancing the visibility of internal organs and tissues during imaging. However, its use must be carefully monitored to minimize the risk of adverse reactions and environmental damage. Further research is needed to fully understand the potential benefits and risks of iotalamic acid and to develop new and improved contrast agents.
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@thebiotek.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@thebiotek.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.
Category
Hot Products
D-ribose-L-cysteine
CAS No.: 232617-15-1
Sterubin
CAS No.: 51857-11-5
Troparil, (+)-
CAS No.: 74163-84-1
![N-Phenyl-d5-N'-[1-(2-phenylethyl)]-4-piperidine](/images/structure/BT-1439938.png)
N-Phenyl-d5-N'-[1-(2-phenylethyl)]-4-piperidine
CAS No.: 1189466-15-6
POE (15) tallow amine
CAS No.: 61791-26-2
5-Cholesten-3beta-25-diol-3-sulfate
CAS No.: 884905-07-1
info@thebiotek.com
256 N Vinedo Ave, Pasadena, California 91107
