纳甲硫酸盐和纳多纳甲硫酸盐
Christina Burnett1, Wilma F Bergfeld2, Donald V Belsito2
1Cosmetic Ingredient Review, Senior Scientific Analyst/Writer.
International journal of toxicology
|September 28, 2023
概括
化品成分安全专家小组证实,纳二硫酸盐和聚纳二硫酸盐在化品中使用是安全的. 这些成分在当前的产品类型和度中对于皮肤应用是安全的.
科学领域:
- 化品科学 化品科学
- 皮肤病学 皮肤病学
- 毒理学 毒理学 毒理学
背景情况:
- 化品成分安全专家小组此前在2003年对化品成分进行了评估.
- 自最初评估以来,新的研究和更新的使用信息已经可用.
- 监管机构根据新出现的科学数据不断审查成分的安全性.
研究的目的:
- 重新评估甲二硫酸盐和聚甲二硫酸盐的安全性.
- 考虑最新的科学研究和最新的产品使用信息.
- 为了确认这些化品成分在皮肤上应用的安全性.
主要方法:
- 审查最新可用的科学研究.
- 对化品产品类型的最新信息进行分析.
- 评估目前在化品配方中使用的度.
- 专家小组审查和安全确定.
主要成果:
- 专家小组审查了最新的研究和使用数据.
- 纳甲硫酸盐和聚纳甲硫酸盐被评估.
- 发现这些成分对于化品使用是安全的.
结论:
- 纳二硫酸盐和多纳二硫酸盐作为化品成分是安全的.
- 对于描述的使用和度实践,安全性得到证实.
- 这些成分在适用于皮肤的配方中是安全的.
相关概念视频
2° Amines to N-Nitrosamines: Reaction with NaNO2
4.3K
Secondary amines react with nitrous acid to form N-nitrosamines, as depicted in Figure 1. Nitrous acid, a weak and unstable acid, is formed in situ from an aqueous solution of sodium nitrite and strong acids, such as hydrochloric acid or sulfuric acid, in cold conditions. In the presence of an acid, the nitrous acid gets protonated. The subsequent loss of water results in the formation of the electrophile known as nitrosonium ion.
4.3K
Precipitation Reactions
50.9K
In a precipitation reaction, aqueous solutions of soluble salts react to give an insoluble ionic compound – the precipitate. The reaction occurs when oppositely charged ions in solution overcome their attraction for water and bind to each other, forming a precipitate that separates out from the solution. Since such reactions involve the exchange of ions between ionic compounds in aqueous solution, they are also referred to as double displacement, double replacement, exchange reactions, or...
50.9K
Electrophilic Aromatic Substitution: Sulfonation of Benzene
6.1K
Sulfonation of benzene is a reaction wherein benzene is treated with fuming sulfuric acid at room temperature to produce benzenesulfonic acid. Fuming sulfuric acid is a mixture of sulfur trioxide and concentrated sulfuric acid.
6.1K
Nucleophilic Aromatic Substitution: Addition–Elimination (SNAr)
3.8K
Nucleophilic substitution in aromatic compounds is feasible in substrates bearing strong electron-withdrawing substituents positioned ortho or para to the leaving group. The reaction proceeds via two steps: the addition of the nucleophile and the elimination of the leaving group.
The reaction begins with an attack of the nucleophile on the carbon that holds the leaving group. This results in the delocalization of the π electrons over the ring carbons. The resonance interaction between...
The reaction begins with an attack of the nucleophile on the carbon that holds the leaving group. This results in the delocalization of the π electrons over the ring carbons. The resonance interaction between...
3.8K
Nucleophilic Aromatic Substitution of Aryldiazonium Salts: Aromatic SN1
2.1K
Treating arylamines with nitrous acid gives aryldiazonium salts that are effective substrates in nucleophilic aromatic substitution reactions. The diazonio group in these salts can be easily displaced by different nucleophiles, yielding a wide variety of substituted benzenes. The leaving group departs as nitrogen gas, and this easy elimination is the driving force for the substitution reaction.
In the Sandmeyer reaction, for example, the diazonio group is replaced by a chloro, bromo,...
In the Sandmeyer reaction, for example, the diazonio group is replaced by a chloro, bromo,...
2.1K
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview
3.3K
Nitrous acid and nitric acids are two types of acids containing nitrogen, among which nitrous acid is weaker than nitric acid. Nitrous acid with a pKa value of 3.37 ionizes in water to give a nitrite ion and the hydronium ion.
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by...
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by...
3.3K


