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4-Amino-4-methyl-2-pentanone

CAS# 625-04-7

4-Amino-4-methyl-2-pentanone

2D Structure

Catalog No. BCN1772----Order now to get a substantial discount!

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4-Amino-4-methyl-2-pentanone: 5mg $69 In Stock
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Quality Control of 4-Amino-4-methyl-2-pentanone

3D structure

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4-Amino-4-methyl-2-pentanone

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Chemical Properties of 4-Amino-4-methyl-2-pentanone

Cas No. 625-04-7 SDF Download SDF
PubChem ID 69361 Appearance Powder
Formula C6H13NO M.Wt 115.17
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 4-amino-4-methylpentan-2-one
SMILES CC(=O)CC(C)(C)N
Standard InChIKey CQTRUFMMCCOKTA-UHFFFAOYSA-N
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Protocol of 4-Amino-4-methyl-2-pentanone

Structure Identification
Structural Chemistry, 2014, 25(3):707-714.

Transforming aspirin into novel molecular salts of salicylic acid.[Reference: WebLink]

Aspirin is one of the most widely used analgesic, antipyretic, and anti-inflammatory drugs. Herein we disclose a way to transform aspirin into novel multicomponent crystal forms of salicylic acid, also a long-known analgesic with anti-inflammatory properties, among others, covering a broad spectrum of applications, including skin care products.
METHODS AND RESULTS:
A salicylic acid:salicylate ammonium salt and a salicylate:2-methyl-4-oxopentan-2-aminium molecular salt are concomitantly formed in acetone/ammonia solutions, resulting from aspirin decomposition. Furthermore the 2-methyl-4-oxopentan-2-aminium cation results from a sequence of in situ reactions: (i) imine formation, in which acetone is known to undergo under basic pH conditions; (ii) nucleophilic attack of α-carbon of the deprotonated acetone to the imine yielding 4-amino-4-methylpentan-2-one(4-Amino-4-methyl-2-pentanone); and (iii) protonation of 4-amino-4-methylpentan-2-one. In the structures obtained for the novel multicomponent crystal forms, the strong charge-assisted N+–H···O/O− hydrogen bonds between the drug molecule and the co-former play a key function in the supramolecular arrangement. The typical R22(8)carboxylic···carboxylic homosynthon observed in salicylic acid was inhibited by the salt formation.
CONCLUSIONS:
These results are in agreement with the results of a careful survey on the Cambridge Structural Database.

4-Amino-4-methyl-2-pentanone Dilution Calculator

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4-Amino-4-methyl-2-pentanone Molarity Calculator

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Preparing Stock Solutions of 4-Amino-4-methyl-2-pentanone

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 8.6828 mL 43.4141 mL 86.8282 mL 173.6563 mL 217.0704 mL
5 mM 1.7366 mL 8.6828 mL 17.3656 mL 34.7313 mL 43.4141 mL
10 mM 0.8683 mL 4.3414 mL 8.6828 mL 17.3656 mL 21.707 mL
50 mM 0.1737 mL 0.8683 mL 1.7366 mL 3.4731 mL 4.3414 mL
100 mM 0.0868 mL 0.4341 mL 0.8683 mL 1.7366 mL 2.1707 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on 4-Amino-4-methyl-2-pentanone

Synthesis, crystal structure, and magnetic properties of oxime-bridged polynuclear Ni(II) and Cu(II) complexes.[Pubmed:15679406]

Inorg Chem. 2005 Feb 7;44(3):709-15.

Two new polynuclear complexes [Ni6(amox)6(mu6-O)(mu3-OH)2](Cl2).6H2O and [Cu3(amox)3(mu3-OH)(mu3-Cl)](ClO4).4H2O (amox- = anion of 4-Amino-4-methyl-2-pentanone oxime) have been synthesized and characterized structurally and magnetically. The Ni(II) complex contains a novel Chinese-lantern-like Ni6 cage centered by an oxo ion. It contains the nearest octahedral Ni(II)...Ni(II) separation (<2.8 A) and exhibits strong antiferromagnetic properties. The Cu(II) complex has a cyclic trinuclear copper(II) core bridged by both mu3-OH(-) and mu3-Cl(-) ions. The magnetic susceptibilities of both antiferromagnetic complexes were fitted by using approximate models.

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