690953
N,N,N′,N′-Tetramethylguanidine
≥99.0% (GC)
Synonym(s):
1,1,3,3-Tetramethylguanidine
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About This Item
Linear Formula:
(CH3)2NC(=NH)N(CH3)2
CAS Number:
Molecular Weight:
115.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-302-7
Beilstein/REAXYS Number:
969608
MDL number:
Assay:
≥99.0% (GC)
Form:
liquid
Quality Level
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
SMILES string
CN(C)C(=N)N(C)C
InChI
1S/C5H13N3/c1-7(2)5(6)8(3)4/h6H,1-4H3
InChI key
KYVBNYUBXIEUFW-UHFFFAOYSA-N
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
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Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Met. Corr. 1 - Skin Corr. 1B
Storage Class
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
Regulatory Information
危险化学品
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Synthesis and thermal characterization of novel poly (tetramethylsilanthrylenesiloxane) and poly (tetramethylsilphenanthrylenesiloxane) derivatives.
Sato I, et al.
Polymer Bull., 59(5), 607-617 (2007)
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)
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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 690953-10KG | 04061836827885 |
| 690953-25KG | 04061836827908 |
| 690953-1KG | 04061836827892 |