241768
1,1,3,3-Tetramethylguanidine
99%
Synonym(s):
N,N,N′,N′-Tetramethylguanidine
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About This Item
Recommended Products
vapor pressure
0.2 mmHg ( 20 °C)
Quality Level
Assay
99%
form
liquid
refractive index
n20/D 1.469 (lit.)
bp
52-54 °C/11 mmHg (lit.)
density
0.918 g/mL at 25 °C (lit.)
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
Gene Information
human ... EPHX2(2053)
mouse ... Ephx2(13850)
Application
Base employed in the preparation of alkyl nitriles from alkyl halides and 3′-alkylthymidines from 3′-nitrothymidines.
Promotes the pentavalent bismuth oxidation of primary and secondary alchohols to aldehydes and ketones.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Met. Corr. 1 - Skin Corr. 1B
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
122.0 °F - closed cup
Flash Point(C)
50 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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For topical treatment of skin cancer, the design of pH-responsive nanocarriers able to selectively release the drug in the tumor acidic microenvironment represents a reliable option for targeted delivery. In this context, a series of newly synthesized surface-active fatty acid-protic
ChemistryOpen, 6(6), 739-750 (2017-12-12)
Interactions of ribonucleic acid (RNA) with guanidine and guanidine derivatives are important features in RNA-protein and RNA-drug binding. Here we have investigated noncovalently bound complexes of an 8-nucleotide RNA and six different ligands, all of which have a guanidinium moiety
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