CAS 10526-07-5 Benzenamine, 3,3'-(1,3-phenylenebis(oxy))bis- (HCID 66342)

名称と識別子

優先名称: Benzenamine, 3,3'-(1,3-phenylenebis(oxy))bis-
IUPAC: 3-[3-(3-aminophenoxy)phenoxy]aniline
現地名: 1,3-ビス(3-アミノフェノキシ)ベンゼン
英語名: 1,3-Bis(3-aminophenoxy)benzene
分子式: C18H16N2O2
分子量: 292.33

名称と別名

1,3-Bis(3-aminophenoxy)benzeneBenzenamine, 3,3'-[1,3-phenylenebis(oxy)]bis-3,3'-(m-Phenylenedioxy)dianilineEINECS 234-082-6DTXSID4065109Benzenamine, 3,3'-(1,3-phenylenebis(oxy))bis-3,3'-[m-phenylenebis(oxy)]dianiline3,3'-(m-Phenylenebis(oxy))dianilineRefChem:561702DTXCID5032943234-082-610526-07-5

名称をさらに表示

1,3-ビス(3-アミノフェノキシ)ベンゼン3,3'-(m-フェニレン)ビス(オキシ)ビス(ベンゼンアミン)3,3'-(m-フェニレンビスオキシ)ジアニリン3,3'-[(1,3-フェニレン)ビス(オキシ)]ビス(アニリン)3,3'-[m-フェニレンビス(オキシ)]ビスアニリン3,3'-(1,3-フェニレンジオキシ)ジアニリン3,3'-(1,3-フェニレンビスオキシ)ビスアニリン3,3'-(1,3-フェニレンビスオキシ)ビスベンゼンアミン3,3'-(m-フェニレンビスオキシ)ビスアニリン3,3'-[1,3-フェニレンビス(オキシ)]ビスベンゼンアミン3,3'-(1,3-フェニレンビスオキシ)ジアニリン1,3-ビス(m-アミノフェノキシ)ベンゼン3,3'-[1,3-フェニレンビス(オキシ)]ビスアニリン3,3'-[(1,3-フェニレン)ビスオキシ]ビスアニリン3,3'-[3,1-フェニレンビス(オキシ)]ビスアニリン3，3’（mフェニレンジオキシ）ジアニリンレソルシノールビス(3-アミノフェニル)エーテル3，3’-（m-フェニレンジオキシ）ジアニリン3,3′-(m-フェニレンビスオキシ)ジアニリン3,3′-(1,3-フェニレン)ジオキシビスアニリンTPE-M1,3,3-APBAPB-133TIMTEC-BB SBB0083561,3-BIS(3-AMINOPHENO1,3-Bis(3-aminophenoxy3,3'-Phenylenedioxydianiline1,3-Bis(m-aminophenoxy)benzene

3,3'-(1,3-Phenylenebis(oxy))dianiline3-[3-(3-aminophenoxy)phenoxy]anilineMFCD000437183,3'-[1,3-Phenylenebis(oxy)]dianiline3-[3-(3-Aminophenoxy)phenoxy]phenylamine3,3'-(1,3-Phenylenedioxy)dianiline-15N2Resorcinol Bis(3-aminophenyl) Ether1,3-bis-(3-Aminophenoxy)benzene

データベース識別子

CAS: 10526-07-5
PubChem CID: 66342
DTXSID: DTXSID4065109
EC Number: 234-082-6
Nikkaji: J105.954H

物性

構造計算による物性

XLogP: 3.6
極性表面積: 70.5 Å²
水素結合供与体数: 2
水素結合受容体数: 4
回転可能結合数: 4
重原子数: 22
形式電荷: 0
複雑度: 309

物理化学的性質

融点: 108 °C · 108°C
沸点: 479.9 · 479.9±30.0 °C(Predicted)
比重(密度): 1.243 · 1.243
貯蔵温度: Keep in dark place,Inert atmosphere,Room temperature
水溶解度: Insoluble in water
溶解性: Slightly soluble in methanol
外見: powder to crystal
酸解離定数(Pka): 4.29 · 4.29±0.10(Predicted)
色: White to Light yellow to Light orange
InChI: InChI=1S/C18H16N2O2/c19-13-4-1-6-15(10-13)21-17-8-3-9-18(12-17)22-16-7-2-5-14(20)11-16/h1-12H,19-20H2
InChIKey: DKKYOQYISDAQER-UHFFFAOYSA-N
SMILES: C1(OC2C=CC=C(N)C=2)=CC=CC(OC2C=CC=C(N)C=2)=C1
CAS データベース: 10526 · 10526-07-5(CAS DataBase Reference)
EPAの化学物質情報: 3 · Benzenamine, 3,3'-[1,3-phenylenebis(oxy)]bis- (10526-07-5)

化学的性質 · 1 件

化学的特性1,3-Bis(3-aminophenoxy)benzene, also known as TIMTEC-BB SBB008356, is a Light yellow to yellow solid. It has slight solubility in methanol but is insoluble in water. To maintain its stability, it is recommended to store it in a cool and dark place. However, it is incompatible with oxidizing agents and should not be stored or handled near them to avoid any hazardous reactions.

安全と法規制

GHS分類

GHS Classification · 4 件

Warning

H302 (50%): Harmful if swallowed [Warning Acute toxicity, oral]

P261, P264, P270, P271, P272, P273, P280, P301+P317, P302+P352, P304+P340, P317, P321, P330, P333+P317, P362+P364, P391, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 2 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

危険有害性情報

Hazard Classes and CategoriesAcute Tox. 4 (50%)

安全データ

tsca: TSCA listed
hs_code: 29222990
risk_code: 20/21/22
化審法: (3)-3948
safety_code: 26-36/37/39

化学と産業

用途と製造

General Manufacturing InformationBenzenamine, 3,3'-[1,3-phenylenebis(oxy)]bis-: ACTIVE

応用分野

用途有機合成原料。

使用1,3-Bis(3-aminophenoxy)benzene is an intermediate compound used in the production of synthetic materials, such as PI (polyimide) films and polyimide materials.

調製方法 · 1 件

製造方法1,3-Bis(3-aminophenoxy)benzene is a reactive monomer commonly utilized in the synthesis of polyurethane coatings. This compound is processed at 200 degrees Celsius and has a viscosity of 1.5-2.0 centipoise at 25 degrees Celsius. Its chemical structure consists of three amine groups that are ether linked to a benzene ring with one hydroxyl group on the phenoxy side chain. The monomer can be synthesized via acylation reaction or polymerization process, typically through heating with a catalyst. The resulting product is thermally stable and resistant to heat up to 250 degrees Celsius.