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Safety Information

403458

Sigma-Aldrich

N-p-Tosylglycine

97%

Synonym(s):

N-(p-Toluenesulfonyl)glycine

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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

Pictograms

Exclamation mark

Signal Word

Warning

Hazard 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 Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

403458-5G:
403458-1G:
403458-BULK:
403458-VAR:


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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

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