33437
茚三酮
puriss. p.a., ≥99%
别名:
2,2-二羟基-1,3-茚二酮, 苯并戊三酮 一水合物, 苯并环丙三酮 一水合物
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关于此项目
经验公式（希尔记法）:
C9H6O4
化学文摘社编号:
分子量:
178.14
EC Number:
207-618-1
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1910963
MDL number:
InChI key
FEMOMIGRRWSMCU-UHFFFAOYSA-N
InChI
1S/C9H6O4/c10-7-5-3-1-2-4-6(5)8(11)9(7,12)13/h1-4,12-13H
SMILES string
OC1(O)C(=O)c2ccccc2C1=O
grade
puriss. p.a.
assay
≥99%
ign. residue
≤0.1% (as SO4)
pH
4.6-5.0 (20 °C, 1%)
mp
250 °C (dec.) (lit.)
storage temp.
2-8°C
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Application
可以用于检测氨基酸，多肽和蛋白质中的自由氨基基团。
Ninhydrin (triketohydrindene hydrate) may be used as reagent for the quantification of amino acids and peptides by photometric method and colorimetric method. It may be used to prepare the ninhydrin reagent, by mixing ninhydrin and hydrindantin (reduced form of ninhydrin) in dimethyl sulfoxide. This reagent is used in manual ninhydrin method for the quantitative determination of amino acids.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
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, Gloves
法规信息
新产品
此项目有
The determination of amino-acids with ninhydrin.
Yemm EW, et al.
Analyst, 80(948), 209-214 (1955)
Photometric ninhydrin method for use in the chromatography of amino acids.
S MOORE et al.
The Journal of biological chemistry, 176(1), 367-388 (1948-10-01)
Joseph Almog et al.
Journal of forensic sciences, 56 Suppl 1, S162-S165 (2011-01-14)
We explored the quality distribution of ninhydrin-developed prints on A4 bond paper in two groups of individuals, in Israel and in India. While the quality distributions of the developed marks in both countries had some dissimilarities, both groups showed the
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
Jianhui Gu et al.
Journal of tissue engineering and regenerative medicine, 6(2), 163-168 (2011-03-04)
This paper describes a clinical case study in which a chitosan/polyglycolic acid nerve guidance conduit (chitosan-PGA NGC) was utilized to repair a 30 mm long median nerve defect in the right distal forearm of a 55 year-old male patient. Thirty-six
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