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Ninhydrin - Analytical Reagent, high purity , CAS No.485-47-2

  • AR
Item Number
N105629
Grouped product items
SKUSizeAvailabilityPrice Qty
N105629-1g
1g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$9.90
N105629-5g
5g
In stock
$11.90
N105629-25g
25g
In stock
$33.90
N105629-100g
100g
In stock
$119.90
N105629-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$469.90
View related series
Carbonyl compound ketone

Basic Description

SynonymsNINHYDRIN|485-47-2|Ninhydrine|1,2,3-Indantrione monohydrate|Ninhydrin hydrate|2,2-Dihydroxy-1H-indene-1,3(2H)-dione|2,2-Dihydroxy-1,3-indandione|1H-Indene-1,3(2H)-dione, 2,2-dihydroxy-|2,2-Dihydroxyindane-1,3-dione|Triketohydrindene hydrate|2,2-dihydroxyi
Specifications & PurityAR
Biochemical and Physiological MechanismsNinhydrin reacts with primary and secondary amines producing a blue or purple reaction product (diketohydrindylidene-diketohydrindamine). Ninhydrin is commonly used for the development of fingermarks on porous surfaces and is often used in comparison with
Storage TempStore at 2-8°C
Shipped InWet ice
GradeAR
Note10g,1g卖完停产,不再备货
Product Description

Used in the detection and assay of peptides, amino acids, amines, and amino sugars yielding highly fluorescent ternary compounds with aldehydes and primary amines. Reaction with sarcosine or proline gives azomethine ylides.

Application:

It can be used for the detection of peptides, amino acids, amino acids and amino sugars, and can produce strong fluorescent ternary compounds with aldehydes and primary amines. Reacts with sarcosine or proline to form methylimine Ylide. Ninhydrin (ninhydrin hydrate) can be used as a reagent for the determination of amino acids and peptides by photometry and colorimetry. It can also be used to prepare ninhydrin reagents by mixing ninhydrin with hydroninhydrin (reduced form of ninhydrin) in dimethyl sulfoxide. This reagent can be used for the manual ninhydrin method to quantify amino acids. It can be used to detect free amino groups in amino acids, peptides and proteins.

Associated Targets

EHMT2 Tchem Histone-lysine N-methyltransferase EHMT2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NR3C1 Tclin Glucocorticoid receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

EHMT1 Tchem Histone-lysine N-methyltransferase EHMT1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

RORC Tchem Nuclear receptor ROR-gamma 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TSHR Tclin Thyrotropin receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

RECQL Tbio ATP-dependent DNA helicase Q1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ALOX12 Tchem Arachidonate 12-lipoxygenase, 12S-type 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

L3MBTL1 Tchem Lethal(3)malignant brain tumor-like protein 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ALOX15B Tchem Arachidonate 15-lipoxygenase B 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CASP1 Tchem Caspase-1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA1 Tclin Carbonic anhydrase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA2 Tclin Carbonic anhydrase 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA4 Tclin Carbonic anhydrase 4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA9 Tclin Carbonic anhydrase 9 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA7 Tclin Carbonic anhydrase 7 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

BACE1 Tchem Beta-secretase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

AR Tclin Androgen receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ALDH1A1 Tchem Retinal dehydrogenase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TP53 Tchem Cellular tumor antigen p53 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NFE2L2 Tchem Nuclear factor erythroid 2-related factor 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

IDO1 Tchem Indoleamine 2,3-dioxygenase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAPK1 Tchem Mitogen-activated protein kinase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 2,2-dihydroxyindene-1,3-dione
INCHI 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
Canonical SMILES C1=CC=C2C(=C1)C(=O)C(C2=O)(O)O
Isomeric SMILES C1=CC=C2C(=C1)C(=O)C(C2=O)(O)O
WGK Germany 3
RTECS NK5425000
PubChem CID 10236
Molecular Weight 178.14
Beilstein 1910963
Reaxy-Rn 1910963

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

33 results found

Lot NumberCertificate TypeDateItem
F2417302Certificate of AnalysisJun 21, 2024 N105629
F2417301Certificate of AnalysisJun 21, 2024 N105629
F2417300Certificate of AnalysisJun 21, 2024 N105629
F2417286Certificate of AnalysisJun 21, 2024 N105629
E2410320Certificate of AnalysisMay 13, 2024 N105629
E2410319Certificate of AnalysisMay 13, 2024 N105629
E2410251Certificate of AnalysisMay 13, 2024 N105629
E2410252Certificate of AnalysisMay 13, 2024 N105629
E2410253Certificate of AnalysisMay 13, 2024 N105629
E2410254Certificate of AnalysisMay 13, 2024 N105629
E2410316Certificate of AnalysisMay 13, 2024 N105629
E2410317Certificate of AnalysisMay 13, 2024 N105629
E2410318Certificate of AnalysisMay 13, 2024 N105629
L2318059Certificate of AnalysisDec 26, 2023 N105629
G2304994Certificate of AnalysisJul 19, 2023 N105629
K2323061Certificate of AnalysisJul 19, 2023 N105629
G23041004Certificate of AnalysisJul 19, 2023 N105629
G2304991Certificate of AnalysisJul 19, 2023 N105629
G23041003Certificate of AnalysisJul 19, 2023 N105629
G2304999Certificate of AnalysisJul 19, 2023 N105629
G23041002Certificate of AnalysisJul 19, 2023 N105629
F2320045Certificate of AnalysisJul 05, 2023 N105629
E2305525Certificate of AnalysisMay 15, 2023 N105629
E2305517Certificate of AnalysisMay 15, 2023 N105629
B2318155Certificate of AnalysisFeb 23, 2023 N105629
B2318201Certificate of AnalysisFeb 23, 2023 N105629
B2318163Certificate of AnalysisFeb 23, 2023 N105629
B2318157Certificate of AnalysisFeb 23, 2023 N105629
B2318156Certificate of AnalysisFeb 23, 2023 N105629
J22111282Certificate of AnalysisOct 13, 2022 N105629
J22111285Certificate of AnalysisOct 13, 2022 N105629
J22111303Certificate of AnalysisOct 13, 2022 N105629
J22111313Certificate of AnalysisOct 13, 2022 N105629

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Chemical and Physical Properties

SolubilitySoluble in water
SensitivityLight Sensitive
Melt Point(°C)250°C

Safety and Hazards(GHS)

Pictogram(s) GHS07
Signal Warning
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H302:Harmful if swallowed

Precautionary Statements

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P270:Do not eat, drink or smoke when using this product.

P337+P313:IF eye irritation persists: Get medical advice/attention.

P332+P313:IF SKIN irritation occurs: Get medical advice/attention.

P330:Rinse mouth.

P301+P312:IF SWALLOWED: call a POISON CENTER/doctor/... IF you feel unwell.

WGK Germany 3
RTECS NK5425000
Reaxy-Rn 1910963
Merck Index 6554

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