524716
4-Aminophthalic acid
97%
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About This Item
Linear Formula:
H2NC6H3-1,2-(CO2H)2
CAS Number:
Molecular Weight:
181.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
226-596-4
MDL number:
InChI key
OXSANYRLJHSQEP-UHFFFAOYSA-N
InChI
1S/C8H7NO4/c9-4-1-2-5(7(10)11)6(3-4)8(12)13/h1-3H,9H2,(H,10,11)(H,12,13)
SMILES string
Nc1ccc(C(O)=O)c(c1)C(O)=O
assay
97%
reaction suitability
reaction type: solution phase peptide synthesis
mp
344 °C (dec.) (lit.)
application(s)
peptide synthesis
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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F Lloyd et al.
Journal of the National Medical Association, 83(10), 901-904 (1991-10-11)
A standard hybridoma fusion technique was used to produce a monoclonal antibody capable of binding both carcinoembryonic antigen (CEA) and the hapten 4-amino-phthalate. A hypoxanthine-aminopterin-thymidine (HAT) sensitive anti-CEA hybridoma and KLH-phthalate immunized spleen cells were hybridized to yield clones producing
Claudia Wahl et al.
Biotechnology journal, 11(10), 1298-1308 (2016-06-18)
Nucleotide sugars are considered as bottleneck and expensive substrates for enzymatic glycan synthesis using Leloir-glycosyltransferases. Synthesis from cheap substrates such as monosaccharides is accomplished by multi-enzyme cascade reactions. Optimization of product yields in such enzyme modules is dependent on the
Claudia Wahl et al.
Journal of biotechnology, 258, 51-55 (2017-03-30)
The broad substrate spectrum of UDP-sugar pyrophosphorylases from plant salvage pathways is of high interest for the synthesis of expensive nucleotide sugars by straightforward enzyme cascade reactions in combination with monosaccharide kinases. We here present a new UDP-sugar pyrophosphorylase from
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