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424285

Sigma-Aldrich

3-辛基噻吩

97%

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About This Item

经验公式（希尔记法）:
C12H20S
CAS号:
65016-62-8
分子量:
196.35
MDL號碼:
MFCD00085281
分類程式碼代碼:
12352100
PubChem物質ID:
24866561
NACRES:
NA.22

品質等級

100

化驗

97%

形狀

liquid

折射率

n20/D 1.492 (lit.)

bp

106-107 °C/3 mmHg (lit.)

密度

0.92 g/mL at 25 °C (lit.)

SMILES 字串

CCCCCCCCc1ccsc1

InChI

1S/C12H20S/c1-2-3-4-5-6-7-8-12-9-10-13-11-12/h9-11H,2-8H2,1H3

InChI 密鑰

WQYWXQCOYRZFAV-UHFFFAOYSA-N

相关类别

一般說明

3-Octylthiophene is an alkyl thiophene derivative. It has been synthesized by the reaction of 3-bromothiophene with octylmagnesium bromide.

應用

3-Octylthiophene may be used as a starting material in the synthesis of the following:
  • 2,5-dibromo-3-octylthiophene
  • poly(3-butylthiophene)-b-poly(3-octylthiophene), a diblock copoly(3-alkylthiophene)
  • regioregular poly(3-octylthiophene) (POT)

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

235.4 °F - closed cup

閃點（°C）

113 °C - closed cup

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SHBJ8369
SHBF9226V
79196EM
75296HK
02728HH

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2-正己基噻吩 97%

Sigma-Aldrich

693405

2-正己基噻吩

Crystalline diblock conjugated copolymers: Synthesis, self-assembly, and microphase separation of poly (3-butylthiophene)-b-poly (3-octylthiophene).
Wu PT, et al.
Macromolecules, 42(7), 2317-2320 (2009)
Soluble Phenanthrenyl-Imidazole-Presenting Regioregular Poly (3-octylthiophene) Copolymers Having Tunable Bandgaps for Solar Cell Applications.
Chang YT, et al.
Advances in Functional Materials, 17(16), 3326-3331 (2007)
New convenient synthesis of highly regioregular poly (3-octylthiophene) based on the Suzuki coupling reaction.
Guillerez S and Bidan G.
Synthetic Metals, 93(2), 123-126 (1998)
Nannan Jian et al.
Physical chemistry chemical physics : PCCP, 21(13), 7174-7182 (2019-03-20)
Conjugated fluorophores have been extensively used for fluorescence sensing of various substances in the field of life processes and environmental science, due to their noninvasiveness, sensitivity, simplicity and rapidity. Most existing conjugated fluorophores exhibit excellent light-emitting performance in dilute solutions

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