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Merck

21-1510

Sigma-Aldrich

茚三酮

SAJ special grade, ≥98.0%

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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About This Item

经验公式(希尔记法):
C9H6O4
CAS号:
分子量:
178.14
Beilstein:
1910963
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:

等級

SAJ special grade

化驗

≥98.0%

形狀

solid

存貨情形

available only in Japan

mp

250 °C (dec.) (lit.)

SMILES 字串

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

InChI 密鑰

FEMOMIGRRWSMCU-UHFFFAOYSA-N

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應用

可以用于检测氨基酸,多肽和蛋白质中的自由氨基基团。

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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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
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
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
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
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

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