[Reproductive and developmental toxicity of 2- (2H-1, 2, 3-benzotriazol-2-yl) -4-methyl-6- (2-methylpropen-2-yl)

T Guan1, N He, M Li

  • 1Tianjin Centers for Disease Control and Prevention, Tianjin 300011, China.

Insights

The reproductive toxicity of 2-(2H-1,2,3-benzotriazol-2-yl)-4-methyl-6-(2-methylpropen-2-yl)phenol was assessed in mice. The no observed adverse effect level for both male and female Kunming mice was determined to be 146 mg/kg.

Area of Science:

  • Toxicology
  • Reproductive Toxicology
  • Developmental Toxicology

Background:

  • 2-(2H-1,2,3-benzotriazol-2-yl)-4-methyl-6-(2-methylpropen-2-yl)phenol is a chemical requiring toxicological assessment.
  • Understanding its reproductive and developmental effects is crucial for risk assessment.

Purpose of the Study:

  • To investigate the reproductive and developmental toxicity of 2-(2H-1,2,3-benzotriazol-2-yl)-4-methyl-6-(2-methylpropen-2-yl)phenol in mice.
  • To establish a basis for the risk assessment of this chemical.

Main Methods:

  • Kunming mice were orally administered varying doses (0, 146, 292, 584 mg/kg) of the chemical.
  • Reproductive parameters, organ weights, and histopathology were evaluated.
  • Offspring development was monitored.

Main Results:

  • Significant reductions in body weight, food intake, and organ weights were observed in higher dose groups (292 and 584 mg/kg).
  • Offspring exposed to 584 mg/kg showed decreased body weight, length, and tail length.
  • The no observed adverse effect level (NOAEL) was determined to be 146 mg/kg for both sexes.

Conclusions:

  • The no observed adverse effect level (NOAEL) for 2-(2H-1,2,3-benzotriazol-2-yl)-4-methyl-6-(2-methylpropen-2-yl)phenol in male and female Kunming mice is 146 mg/kg.
  • This study provides critical data for the risk assessment of this chemical.

Related Concept Videos

meta-Directing Deactivators: –NO2, –CN, –CHO, –⁠CO2R, –COR, –CO2H01:13

meta-Directing Deactivators: –NO2, –CN, –CHO, –⁠CO2R, –COR, –CO2H

All meta-directing substituents are deactivating groups. These substituents withdraw electrons from the aromatic ring, making the ring less reactive toward electrophilic substitution. For example, the nitration of nitrobenzene is 100,000 times slower than that of benzene because of the deactivating effect of the nitro group. The first step in an electrophilic aromatic substitution is the addition of an electrophile to form a resonance-stabilized carbocation. The energy diagrams for...
6.8K
Predicting Products: SN1 vs. SN202:27

Predicting Products: SN1 vs. SN2

Nucleophilic substitution reactions of alkyl halides can proceed via an SN1 or an SN2 mechanism. While in SN2 reactions, the nucleophile attacks the substrate simultaneously as the leaving group departs, in SN1 reactions, the substrate first dissociates to give the carbocation intermediate. Various factors such as the structure of the substrate, the strength of the nucleophile, and the nature of the solvent promote one mechanism over the other.
With increased substitution on the alkyl halide,...
17.4K
2° Amines to N-Nitrosamines: Reaction with NaNO201:20

2° Amines to N-Nitrosamines: Reaction with NaNO2

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.
5.5K
Criteria for Aromaticity and the Hückel 4n + 2 Rule01:20

Criteria for Aromaticity and the Hückel 4n + 2 Rule

Like benzene, cyclobutadiene and cyclooctatetraene are cyclic compounds with alternate single and double bonds. However, their chemical behavior differs from benzene, as they are unstable and not aromatic. So, what are the structural characteristics of unsaturated compounds categorized as aromatic?  
For the first time, Eric Hückel, a German chemical physicist, derived a set of structural features for a compound to be classified as aromatic. This is now known as Hückel’s rule or the 4n +...
13.7K
SN2 Reaction: Kinetics02:14

SN2 Reaction: Kinetics

Kinetic Studies and Significance
In a chemical reaction, a relationship exists between the concentration of reactants and the rate at which the reaction proceeds. The study to measure this relationship is known as the kinetics of a chemical reaction. Kinetic studies are used to deduce the rate law of a chemical reaction, which provides information about the species involved during the transition state of the rate-determining step. Thus, kinetic studies help to derive the mechanism of a...
10.4K
SN2 Reaction: Mechanism02:27

SN2 Reaction: Mechanism

The kinetic studies of SN2 reactions suggest an essential feature of its mechanism: it is a single-step process without intermediates. Here, both the nucleophile and the substrate participate in the rate-determining step.
The presence of the more electronegative halogen in the substrate creates a polarized carbon-halide bond. The halide pulls the electron cloud generating an electrophilic center at the carbon atom. Thus, the carbon atom carries a partial positive charge while the halide has a...
17.6K