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471518

Sigma-Aldrich

2-(叔丁氨基)乙醇

99%

同義詞:

N-叔丁基乙醇胺

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About This Item

線性公式:
(CH3)3CNHCH2CH2OH
CAS號碼:
分子量::
117.19
Beilstein:
1732684
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:

蒸汽密度

4 (vs air)

化驗

99%

形狀

solid

bp

90-92 °C/25 mmHg (lit.)

mp

41-43 °C (lit.)

密度

0.867 g/mL at 25 °C (lit.)

SMILES 字串

CC(C)(C)NCCO

InChI

1S/C6H15NO/c1-6(2,3)7-4-5-8/h7-8H,4-5H2,1-3H3

InChI 密鑰

IUXYVKZUDNLISR-UHFFFAOYSA-N

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一般說明

2-(tert-Butylamino)ethanol (TBAE) is an alkanolamine. Its dissociation constant has been evaluated at several temperatures. It is a sterically hindered amine and is a useful chemical absorbent for the selective absorption of hydrogen sulfide in the presence of carbon dioxide. The physical solubility of hydrogen sulfide in aqueous solutions of TBAE neutralized with hydrochloric acid has been tested. The obtained solubility data was correlated using the van-Krevelen-Hoftijzer method.

應用

2-(tert-Butylamino)ethanol may be used in the synthesis of 3-tert-butyl-2,2-diphenyl-1,3-oxazaborolidine.

象形圖

Skull and crossbonesCorrosion

訊號詞

Danger

危險聲明

危險分類

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

儲存類別代碼

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

No data available

閃點(°C)

No data available

個人防護裝備

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


分析證明 (COA)

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Effect of carbon dioxide loading on the solubility of nitrous oxide in aqueous solutions of 2-(tert-butylamino) ethanol.
Munder B, et al.
Journal of Chemical and Engineering Data, 45(6), 1195-1195 (2000)
Physical solubility of hydrogen sulfide in aqueous solutions of 2-(tert-butylamino) ethanol.
Munder B, et al.
Journal of Chemical and Engineering Data, 45(6), 1201-1204 (2000)
Yuliya Dobrydneva et al.
Molecular pharmacology, 69(1), 247-256 (2005-10-11)
We have synthesized a series of 2-aminoethoxydiphenyl borate (2-APB, 2,2-diphenyl-1,3,2-oxazaborolidine) analogs and tested their ability to inhibit thrombin-induced Ca(2+) influx in human platelets. The analogs were either synthesized by adding various substituents to the oxazaborolidine ring (methyl, dimethyl, tert-butyl, phenyl
Dissociation constants of some alkanolamines at 293, 303, 318, and 333 K.
Little RJ, et al.
Journal of Chemical and Engineering Data, 35(3), 276-277 (1990)

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