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696099

Sigma-Aldrich

2,3-Diaminobenzoic acid

95%

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About This Item

Fórmula empírica (notación de Hill):
C7H8N2O2
Peso molecular:
152.15
MDL number:
MFCD00137818
UNSPSC Code:
12352200
PubChem Substance ID:
329761798

assay

95%

mp

198-204 °C

application(s)

peptide synthesis

SMILES string

Nc1cccc(C(O)=O)c1N

InChI

1S/C7H8N2O2/c8-5-3-1-2-4(6(5)9)7(10)11/h1-3H,8-9H2,(H,10,11)

InChI key

KKTUQAYCCLMNOA-UHFFFAOYSA-N

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Geun Woo Dong et al.
Clinical and experimental otorhinolaryngology, 2(1), 13-19 (2009-05-13)
Despite the ongoing development of treatment protocols for laryngeal squamous cell carcinoma (LSCC), the patients suffering with this malady have shown only a modestly improved outcome. This poor outcome has been attributed to the lack of therapy that's individualized to
Takeshi Matsumoto et al.
Scientific reports, 8(1), 14623-14623 (2018-10-04)
We report the photochemical carboxylation of o-phenylenedimamine in the absence of a base and an electron donor under an atmosphere of CO2, which afforded 2,3-diaminobenzoic acid (DBA) in 28% synthetic yield and 0.22% quantum yield (Φ(%)). The synthetic yield of
Anal Jana et al.
Journal of photochemistry and photobiology. B, Biology, 214, 112091-112091 (2020-12-08)
Formaldehyde (FA), a simple reactive carbonyl molecule, is endogenously produced in the cell at various physiological condition. At elevated level, FA causes severe cell toxicity as well as damage in macromolecules such proteins and DNA. For detecting FA in living
Bettina S Buchmaier et al.
PloS one, 8(7), e68301-e68301 (2013-07-23)
Osmotic stress has been shown to regulate cytoskeletal protein expression. It is generally known that vimentin is rapidly degraded during apoptosis by multiple caspases, resulting in diverse vimentin fragments. Despite the existence of the known apoptotic vimentin fragments, we demonstrated
Alexander von Tesmar et al.
Cell chemical biology, 24(10), 1216-1227 (2017-09-12)
In vitro reconstitution and biochemical analysis of natural product biosynthetic pathways remains a challenging endeavor, especially if megaenzymes of the nonribosomal peptide synthetase (NRPS) type are involved. In theory, all biosynthetic steps may be deciphered using mass spectrometry (MS)-based analyses of
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