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Key Documents

A62809

Sigma-Aldrich

3-Amino-4-methylbenzoic acid

99%

Synonym(s):

3-Amino-p-toluic acid

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About This Item

Linear Formula:
H2NC6H3(CH3)CO2H
CAS Number:
Molecular Weight:
151.16
Beilstein:
2082449
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

form

powder, crystals or chunks

reaction suitability

reaction type: solution phase peptide synthesis

color

white to purple

mp

164-168 °C (lit.)

application(s)

peptide synthesis

SMILES string

Cc1ccc(cc1N)C(O)=O

InChI

1S/C8H9NO2/c1-5-2-3-6(8(10)11)4-7(5)9/h2-4H,9H2,1H3,(H,10,11)

InChI key

XKFIFYROMAAUDL-UHFFFAOYSA-N

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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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Weixiang Liu et al.
Carbohydrate polymers, 160, 97-105 (2017-01-25)
A novel type of O-carboxymethyl chitosan Schiff bases (O-CSPX) was synthesized via a condensation reaction. After the coordination reaction of cupric ions, Cu(II) complexes (O-CSPX-Cu) were achieved. The theoretical structure of O-CSPX-Cu calculated by Gaussian 09 reveals that the copper

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