690953
四甲基胍
≥99.0% (GC)
别名:
1,1,3,3-四甲基胍
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关于此项目
线性分子式:
(CH3)2NC(=NH)N(CH3)2
化学文摘社编号:
分子量:
115.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-302-7
Beilstein/REAXYS Number:
969608
MDL number:
产品名称
四甲基胍, ≥99.0% (GC)
InChI key
KYVBNYUBXIEUFW-UHFFFAOYSA-N
InChI
1S/C5H13N3/c1-7(2)5(6)8(3)4/h6H,1-4H3
SMILES string
CN(C)C(=N)N(C)C
assay
≥99.0% (GC)
form
liquid
impurities
≤0.50% water
color
APHA: ≤150
bp
162-163 °C (lit.)
density
0.916 g/mL at 20 °C (lit.)
functional group
amine
Quality Level
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Application
N,N,N′,N′-Tetramethylguanidine can be used to synthesize:
- dinucleoside phosphotriester1
- 1,1,3,3-tetramethylguanidinium 2-ethylhexoate2
- tetramethylguanidine ionic liquid (TMG IL)3
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Met. Corr. 1 - Skin Corr. 1B
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
122.0 °F - closed cup
flash_point_c
50 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Synthesis and thermal characterization of novel poly (tetramethylsilanthrylenesiloxane) and poly (tetramethylsilphenanthrylenesiloxane) derivatives.
Sato I, et al.
Polymer Bull., 59(5), 607-617 (2007)
Deoxyribonucleoside cyclic N-acylphosphoramidites as a new class of monomers for the stereocontrolled synthesis of oligothymidylyl-and oligodeoxycytidylyl-phosphorothioates.
Wilk A, et al.
Journal of the American Chemical Society, 122(10), 2149-2156 (2000)
Tetramethyl guanidinium chlorosulfonate as a highly efficient and recyclable organocatalyst for the preparation of bis (indolyl) methane derivatives.
Kalla R, et al.
Catalysis Communications, 57, 55-59 (2014)
G V S M Carrera et al.
Faraday discussions, 183, 429-444 (2015-09-22)
In this report, novel systems, based on highly abundant saccharides, D-mannose, D-glucose, β-cyclodextrin, alginic acid and mannitol, in combination with an organic superbase, tetramethylguanidine (TMG) or 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), are studied for carbon dioxide capture. With D-mannose and D-glucose, several ratios
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