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Merck

317594

Sigma-Aldrich

三甲胺N-氧化物

95%

别名:

TMANO

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About This Item

线性分子式:
(CH3)3N(O)
CAS号:
分子量:
75.11
EC號碼:
MDL號碼:
分類程式碼代碼:
12352116
PubChem物質ID:
NACRES:
NA.22

化驗

95%

反應適用性

reagent type: oxidant

mp

220-222 °C (lit.)

SMILES 字串

C[N+](C)(C)[O-]

InChI

1S/C3H9NO/c1-4(2,3)5/h1-3H3

InChI 密鑰

UYPYRKYUKCHHIB-UHFFFAOYSA-N

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一般說明

三甲胺N-氧化物是一种有机化合物,属于氧化胺类。它通常存在于海洋生物的组织中,可以帮助保护它们免受盐碱、静水压力、温度和高尿素等恶劣条件的侵害。

應用

三甲胺N-氧化物可用于:
  • 用作有机金属化合物的脱金属和脱羰试剂
  • 与二异丙基氨基锂反应制备甲亚胺叶立德。进而与简单的烯烃反应制得相应的吡咯烷。
  • 介导硫醇到二硫化物的转化。

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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J Klysik et al.
FEBS letters, 333(3), 261-267 (1993-11-01)
The ability of the Escherichia coli single-stranded DNA-binding protein (SSB) to recognize structural features associated with intramolecular triplex formation in oligopurine.oligopyrimidine (pur.pyr) inserts in recombinant plasmids was evaluated. The SSB protein binds to supercoiled plasmids and causes a site-preferential increase
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Ingham WL and Coville NJ
Inorganic Chemistry, 31(20), 4084-4090 (1992)
Hydride ion transfer from carbon-hydrogen bonds to carbon disulfide, carbonyl sulfide, and carbon dioxide. Synthesis, reactivity, and structure of manganese complexes (η 5-C6MenH7-n) Mn (CO) LL'
Snyder DB, et al.
Journal of the American Chemical Society, 115(15), 6718-6729 (1993)
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