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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:
1080-44-0
Molecular Weight:
229.25
MDL number:
MFCD00045898
UNSPSC Code:
12352209
PubChem Substance ID:
24865195
NACRES:
NA.22
Pricing and availability is not currently available.

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
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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

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Certificates of Analysis (COA)

Lot/Batch Number
09630CE
04415MB
12119LN
09026KQ
08803KN

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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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