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N0507
Ninhydrin Sprühreagenz
0.2% in ethanol
Synonym(e):
Ninhydrin -Lösung
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About This Item
Empirische Formel (Hill-System):
C9H6O4
CAS-Nummer:
Molekulargewicht:
178.14
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
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Form
liquid
Qualitätsniveau
Konzentration
0.2% in ethanol
Lagertemp.
2-8°C
SMILES String
OC1(O)C(=O)c2ccccc2C1=O
InChI
1S/C9H6O4/c10-7-5-3-1-2-4-6(5)8(11)9(7,12)13/h1-4,12-13H
InChIKey
FEMOMIGRRWSMCU-UHFFFAOYSA-N
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Anwendung
amino acids, amines and amino sugars.
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Matthew G Romei et al.
Science (New York, N.Y.), 367(6473), 76-79 (2020-01-04)
Rotation around a specific bond after photoexcitation is central to vision and emerging opportunities in optogenetics, super-resolution microscopy, and photoactive molecular devices. Competing roles for steric and electrostatic effects that govern bond-specific photoisomerization have been widely discussed, the latter originating
Chao Li et al.
Journal of biomaterials science. Polymer edition, 23(1-4), 405-424 (2011-02-12)
Biomaterials have been playing important roles in cartilage regeneration. Although many scaffolds have been reported to enhance cartilage regeneration, none of the scaffolds available are optimal regarding mechanical properties, integration with host cartilage and providing proper micro-environment for chondrocyte attachment
Yu-Feng Xie et al.
Journal of neurochemistry, 122(3), 605-618 (2012-05-23)
Neurons located in the trigeminal subnucleus caudalis (Vc) play crucial roles in pain and sensorimotor functions in the orofacial region. Because of many anatomical and functional similarities with the spinal dorsal horn (SDH), Vc has been termed the medullary dorsal
Darren B Hansen et al.
Chemical Society reviews, 34(5), 408-417 (2005-04-27)
Following its discovery by Siegfried Ruhemann in 1910, ninhydrin rapidly became a practical analytical tool. In 1954 it was found to be an important reagent to develop fingerprints on porous surfaces. Since its use in forensic chemistry, many efforts have
Mendel Friedman
Journal of agricultural and food chemistry, 52(3), 385-406 (2004-02-05)
The reaction of ninhydrin with primary amino groups to form the purple dye now called Ruhemann's purple (RP) was discovered by Siegfried Ruhemann in 1910. In addition, imines such as pipecolic acid and proline, the guanidino group of arginine, the
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