8.22256
Aniline
for synthesis
Synonym(s):
Aniline, Aminobenzene, Phenylamine, Benzenamine
About This Item
Recommended Products
vapor pressure
0.5 hPa ( 20 °C)
Quality Level
Assay
≥99.0% (GC)
form
liquid
autoignition temp.
540 °C
potency
840 mg/kg LD50, skin (Rabbit)
expl. lim.
1.2-11 % (v/v)
pH
8.8 (20 °C, 36 g/L in H2O)
bp
184 °C/1013 hPa
mp
-6.2 °C
transition temp
flash point 76 °C
solubility
36 g/L
density
1.02 g/cm3 at 20 °C
storage temp.
2-30°C
InChI
1S/C6H7N/c7-6-4-2-1-3-5-6/h1-5H,7H2
InChI key
PAYRUJLWNCNPSJ-UHFFFAOYSA-N
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Application
- One pot conversion of phenols and anilines to aldehydes and ketones: Exploiting α gem boryl carbanions, this study offers a method compatible with a diverse range of phenols and anilines, facilitating simpler synthetic pathways in organic chemistry (Das et al., 2024).
- In-silico-assisted derivatization of triarylboranes: This research discusses a catalytic method for the reductive alkylation of aniline-derived amino acids, improving functional-group compatibility in peptide modification (Hisata et al., 2024).
- C–heteroatom coupling with electron-rich aryls: Utilizing nickel catalysis and light, this method enhances the synthesis of anilines and aryl ethers, contributing to more efficient organic synthesis processes (Cornella et al., 2024).
Analysis Note
Density (d 20 °C/ 4 °C): 1.020 - 1.022
Identity (IR): passes test
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Dam. 1 - Muta. 2 - Skin Sens. 1 - STOT RE 1
Target Organs
Blood
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
Flash Point(F)
158.0 °F - closed cup
Flash Point(C)
70 °C - closed cup
Certificates of Analysis (COA)
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