产品名称
3-氨基邻苯二甲酰亚胺, 97%
InChI
1S/C8H6N2O2/c9-5-3-1-2-4-6(5)8(12)10-7(4)11/h1-3H,9H2,(H,10,11,12)
SMILES string
Nc1cccc2C(=O)NC(=O)c12
InChI key
GQBONCZDJQXPLV-UHFFFAOYSA-N
assay
97%
mp
268.5-273.5 °C (lit.)
Application
3-Aminophthalimide may be used in direct chemiluminescent cellular bioassays. It may also be used in the preparation of 3-bromopthalimide.
General description
3-Aminophthalimide (API) is a stable precursor of luminol. API can be prepared by the hydrogenation of 3-nitrophthalimide and methanol in the presence of 10% Pd-C.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Demetra Mavri-Damelin et al.
Bioconjugate chemistry, 20(2), 266-273 (2009-01-15)
We present a labeling system for direct chemiluminescence-based cellular bioassays using the stable pro-chemiluminescent, luminol precursor, 3-aminophthalimide (API). API-coupled reporter molecules are detected chemiluminometrically after treatment with hydrazine, which converts the API label to luminol. API derivatives containing a variety
177. Chemiluminescent organic compounds. Part VII. Substituted phthalaz-1: 4-diones. Effect of substituents on the luminescent power.
Drew HDK and Garwood RF.
Journal of the Chemical Society, 836-837 (1939)
A Study of the Aminophthalimidoacetic Acids1.
Caswell LR and Atkinson PC.
The Journal of Organic Chemistry, 29(11), 3151-3154 (1964)
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