268151
三乙胺缓冲物质，用于生物化学 盐酸盐
reagent grade, 98%
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线性分子式:
(C2H5)3N · HCl
化学文摘社编号:
分子量:
137.65
EC Number:
209-067-2
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
3906409
MDL number:
InChI key
ILWRPSCZWQJDMK-UHFFFAOYSA-N
InChI
1S/C6H15N.ClH/c1-4-7(5-2)6-3;/h4-6H2,1-3H3;1H
SMILES string
Cl.CCN(CC)CC
grade
reagent grade
assay
98%
mp
261 °C (dec.) (lit.)
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
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Eugenio Hardy et al.
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Nanoaggregates composed of selected glycoforms from Escherichia coli 055:B5 lipopolysaccharide (LPS) were prepared by combining sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis, zinc-imidazole reverse staining, zinc chelation after cutting gel slices, elution with either 0.5% triethylamine (TEA) or 0.4% to 0.5%
Sven Hansen et al.
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Water reduction systems that use a bis-cyclometalated Ir(III) photosensitiser (PS) along with homogeneous Pd complexes as a source of in-situ-formed colloidal Pd as the water reducing complex (WRC) and triethylamine (TEA) as the sacrificial electron donor were tested and characterised
Sumanta Kumar Padhi et al.
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Cyclometalated ruthenium complexes having C(^)N and N(^)C type coordinating ligands with NAD(+)/NADH function have been synthesized and characterized by spectroscopic methods. The variation of the coordinating position of σ-donating carbon atom leads to a drastic change in their properties. Both
Juan M Padró et al.
Analytica chimica acta, 725, 87-94 (2012-04-17)
A new automated and rapid potentiometric method for determining the effect of organic-solvent composition on pK(a) has been developed. It is based on the measurements of pH values of buffer solutions of variable solvent compositions using a combined glass electrode.
Xinshuai Zhang et al.
Angewandte Chemie (International ed. in English), 51(29), 7282-7286 (2012-06-15)
A matter of protection: The outcome of a divergent organocatalytic aza-Michael/aldol cascade process toward quinolines and 1,4-dihydroquinolines depends on the choice of the N-protecting group (see scheme; TEA = triethylamine, TMS = trimethylsilyl). Use of an electron-donating sulfonyl group results
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