Iodopropynyl Butylcarbamate

• CAS: 55406-53-6 / 57-55-6
• Catalog Number: ACM55406536
• Category: Other Products
• Molecular Weight: 281.09
• Molecular Formula: C₈H₁₂INO₂
• Description: Liquid preservative for various cosmetic applications.
• Solubility: Miscible in propylene glycol
• Appearance: Pale yellow liquid, slight iodine odor
• Application: All kinds of skin and hair care products
• Storage: Store light-protected at a cool and dry place
• HS Code: 2905310000

Custom Q&A

Is Iodopropynyl Butylcarbamate safe to use?

Iodopropynyl Butylcarbamate is not entirely safe to use as it is a suspected gastrointestinal and liver toxin. It is also thought to present risks to human reproduction and development, potentially leading to reduced fertility and increased risk of pregnancy problems. Additionally, it is a suspected teratogen, meaning it may increase the risk of birth defects.

What are the concerns about Iodopropynyl Butylcarbamate's toxicity?

There are concerns about toxicity with Iodopropynyl Butylcarbamate, as noted by the Cosmetic Ingredient Review (CIR). It is recommended to limit its use in cosmetics to concentrations less than or equal to 0.1%. Higher concentrations have the potential to irritate the skin, and it is not recommended for use in aerosolized products due to the dangers of inhalation.

How does the European Union regulate the use of Iodopropynyl Butylcarbamate in cosmetics?

The European Union limits the use of Iodopropynyl Butylcarbamate in cosmetics to a maximum concentration of 0.02% in rinse-off products and 0.01% in leave-on products. However, in deodorant/antiperspirant products, the limit is even lower at 0.0075%.

What are the symptoms of an allergy to Iodopropynyl Butylcarbamate?

Typical symptoms of an allergy to Iodopropynyl Butylcarbamate include redness, swelling, itching, and fluid-filled blisters. It is important to note that these symptoms may not develop immediately and may take several days after exposure to the ingredient to appear.

What are some alternative natural preservatives to Iodopropynyl Butylcarbamate?

Thyme, vitamin E, vitamin C, lavender, and rosemary are all natural alternatives to chemicals like Iodopropynyl Butylcarbamate. These ingredients not only preserve the formula but also provide additional skin benefits.

What is the origin of Iodopropynyl Butylcarbamate?

Iodopropynyl Butylcarbamate is synthesized through a reaction between iodine, butylamine, and carbamic acid. This reaction forms the Iodopropynyl Butylcarbamate compound, which is then further processed and purified to obtain the final product.

What is Iodopropynyl Butylcarbamate used for in the cosmetics industry?

Iodopropynyl Butylcarbamate is used in the cosmetics industry for its antimicrobial properties and preservative capabilities. It is added to various cosmetic formulations to prevent the growth of bacteria, yeast, and mold, extending the shelf life of the products.

What types of cosmetic products commonly contain Iodopropynyl Butylcarbamate?

Iodopropynyl Butylcarbamate can be found in a wide range of cosmetic products, including foundations, concealers, bronzers, self-tanners, eye shadows, mascaras, makeup removers, shampoos, conditioners, shaving creams, diaper creams, anti-itch and rash creams, bath soaks, body washes, hair dyes, lip balms, and moisturizers.

What is the chemical formula of Iodopropynyl Butylcarbamate?

The chemical formula of Iodopropynyl Butylcarbamate is C9H12IN3O2.

How is Iodopropynyl Butylcarbamate solubility described?

Iodopropynyl Butylcarbamate is soluble in both water and oil-based systems.

Synthetic Use

Upstream Synthesis Route 1

• 57272-05-6
• 109-73-9

• 55406-53-6

Reference: [1] Patent: CN107963983, 2018, A, . Location in patent: Paragraph 0007; 0021-0024

Upstream Synthesis Route 2

• 76114-73-3

• 55406-53-6

Reference: [1] Patent: WO2005/16871, 2005, A1, . Location in patent: Page/Page column 10-11; 12-13

Downstream Synthesis Route 1

• 76114-73-3

• 55406-53-6

Reference: [1]Patent: WO2005/16871,2005,A1 .Location in patent: Page/Page column 10-11; 12-13

* For details of the synthesis route, please refer to the original source to ensure accuracy.