4-Amino-4-methyl-2-pentanone | CAS:625-04-7

4-Amino-4-methyl-2-pentanone

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4-Amino-4-methyl-2-pentanone Description

Source:
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage:	Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C). Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
After receiving:	The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.

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.

Product Name	4-Amino-4-methyl-2-pentanone
Price:
CAS No.:	625-04-7
Catalog No.:	CFN00045
Molecular Formula:	C₆H₁₃NO
Molecular Weight:	115.17 g/mol
Purity:	>=98%
Type of Compound:	Alkaloids
Physical Desc.:	Powder
Source:
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download:	COA MSDS SDF
Similar structural:	Comparison (Web) (SDF)
Guestbook:

Size /Price /Stock	10 mM * 100 uL in DMSO / Inquiry / In-stock 10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries	Alkaloids Compound Library

	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

CFN00074	2-(Dimethylamino)ethanol	108-01-0	89.14	C₄H₁₁NO
CFN00022	2-(Dimethylamino)ethanesulfonic acid	637-95-6	153.2	C₄H₁₁NO₃S
CFN00034	2-Dimethylaminoethylphosphonic acid	14596-56-6	153.12	C₄H₁₂NO₃P
CFN00045	4-Amino-4-methyl-2-pentanone	625-04-7	115.17	C₆H₁₃NO
CFN00046	1-Amino-2-methylpropan-2-ol	2854-16-2	89.14	C₄H₁₁NO
CFN00047	2-(Dimethylaminomethyl)-2-propanol	14123-48-9	117.19	C₆H₁₅NO
CFN00066	3-(Carboxymethylamino)propanoic acid	505-72-6	147.13	C₅H₉NO₄
CFN00067	Choline sulphate	4858-96-2	183.23	C₅H₁₃NO₄S
CFN00071	Demanyl phosphate	6909-62-2	169.12	C₄H₁₂NO₄P
CFN00073	Diethanolamine	111-42-2	105.14	C₄H₁₁NO₂