403458
N-p-Tosylglycine
97%
Synonym(s):
N-(p-Toluenesulfonyl)glycine
Sign Into View Organizational & Contract Pricing
Select a Size
About This Item
Linear Formula:
CH3C6H4SO2NHCH2CO2H
CAS Number:
Molecular Weight:
229.25
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.22
Assay
97%
form
solid
reaction suitability
reaction type: solution phase peptide synthesis
mp
147-149 °C (lit.)
application(s)
peptide synthesis
SMILES string
Cc1ccc(cc1)S(=O)(=O)NCC(O)=O
InChI
1S/C9H11NO4S/c1-7-2-4-8(5-3-7)15(13,14)10-6-9(11)12/h2-5,10H,6H2,1H3,(H,11,12)
InChI key
VDKFCCZUCXYILI-UHFFFAOYSA-N
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
A Sener et al.
Biochemical pharmacology, 34(14), 2495-2499 (1985-07-15)
N-p-tosylglycine, which inhibits transglutaminase activity in islet homogenates, was found to cause a rapid and sustained facilitation of insulin release evoked by D-glucose, L-leucine or the association of Ba2+ and theophylline in intact islets. Such a facilitating action could not
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service