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資料

N0507

ニンヒドリン溶液

Name: ニンヒドリン 溶液
Brand: SIGMA

0.2% in ethanol

別名:

Ninhydrin solution

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すべての画像(1)

About This Item

実験式（ヒル表記法）:

C₉H₆O₄

CAS番号:

485-47-2

分子量:

178.14

MDL番号:

MFCD00003791

UNSPSCコード:

12352100

PubChem Substance ID:

329818441

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Sigma-Aldrich

N1286

ニンヒドリンスプレー試薬

Sigma-Aldrich

N7285

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Supelco

1.06705

Ninhydrin spray solution

Sigma-Aldrich

151173

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Sigma-Aldrich

N4876

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Supelco

44578

ドラーゲンドルフ試薬

Supelco

17975

Ninhydrin reagent according to Stahl

Supelco

1.06762

Ninhydrin

Supelco

1.02035

Dragendorff′s reagent spray solution

Sigma-Aldrich

M1942

モリブデンブルースプレー試薬

形状

liquid

品質水準

200

濃度

0.2% in ethanol

保管温度

2-8°C

SMILES記法

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 Key

FEMOMIGRRWSMCU-UHFFFAOYSA-N

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アプリケーション

amino acids, amines and amino sugars.

以下による置換

製品番号

詳細

価格

N1286

ニンヒドリンスプレー試薬

試験成績書（COA）

製品のロット番号・バッチ番号を入力して、試験成績書（COA）を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。

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文書ライブラリで、最近購入した製品の文書を検索できます。

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Electrostatic control of photoisomerization pathways in proteins.

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

A viscoelastic chitosan-modified three-dimensional porous poly(L-lactide-co-ε-caprolactone) scaffold for cartilage tissue engineering.

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

The development of novel ninhydrin analogues.

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

Locally released small (non-protein) ninhydrin-reacting molecules underlie developmental differences of cultured medullary versus spinal dorsal horn neurons.

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

Applications of the ninhydrin reaction for analysis of amino acids, peptides, and proteins to agricultural and biomedical sciences.

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

資料

ニンヒドリン溶液