Cas no 13031-62-4 (4-Aminobutyramide Hydrochloride)
4-Aminobutyramide Hydrochloride Chemical and Physical Properties
Names and Identifiers
-
- 4-Aminobutanamide hydrochloride
- 4-Aminobutyramide Hydrochloride
- Butanamide, 4-amino-,hydrochloride (1:1)
- 4-Amino-Butanamide Hydrochloride
- 4-Aminobutyramide HCl
- 4-aminobutyramide monohydrochloride
- 4-aminobutyric acid amide hydrochloride
- EINECS 235-895-9
- Gabamide Hydrochloride
- Gabamide Hydrochlorid
- 4-Aminobutanamide Monohydrochloride
- ButanaMide, 4-aMino-, Monohydrochloride
- AMY15220
- SY174709
- EN300-39439
- 4-aminobutanamidehydrochloride
- Gabaminde hydrochloride
- J-005789
- FT-0661642
- C72206
- MVEPJLNIXKEKMI-UHFFFAOYSA-N
- Butanamide, 4-amino-, hydrochloride (1:1)
- 4-AMINOBUTANAMIDE HCL
- Z398513418
- CBB62LLN98
- AS-64833
- CS-0103894
- MFCD00792526
- 13031-62-4
- NS00085182
- AKOS016008821
- 4-aminobutanamide;hydrochloride
- DTXSID60156451
- SCHEMBL856415
- 4-Aminobutanamide Monohydrochloride; Gabamide Hydrochloride;
- BUTANAMIDE, 4-AMINO- (9CI) HYDROCHLORIDE
- 4-AMINOBUTYRAMIDE, HYDROCHLORIDE
-
- MDL: MFCD00792526
- Inchi: 1S/C4H10N2O.ClH/c5-3-1-2-4(6)7;/h1-3,5H2,(H2,6,7);1H
- InChI Key: MVEPJLNIXKEKMI-UHFFFAOYSA-N
- SMILES: Cl.O=C(CCCN)N
Computed Properties
- Exact Mass: 138.05600
- Monoisotopic Mass: 138.056
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 8
- Rotatable Bond Count: 3
- Complexity: 62.7
- Covalently-Bonded Unit Count: 2
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 69.1A^2
Experimental Properties
- Boiling Point: 300.8°Cat760mmHg
- Flash Point: 135.7°C
- PSA: 69.11000
- LogP: 1.41320
4-Aminobutyramide Hydrochloride Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-IK216-100mg |
4-Aminobutyramide Hydrochloride |
13031-62-4 | 95+% | 100mg |
541CNY | 2021-05-07 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-IK216-250mg |
4-Aminobutyramide Hydrochloride |
13031-62-4 | 95+% | 250mg |
1294CNY | 2021-05-07 | |
| TRC | A603001-25mg |
4-Aminobutyramide Hydrochloride |
13031-62-4 | 25mg |
$ 138.00 | 2023-04-19 | ||
| TRC | A603001-50mg |
4-Aminobutyramide Hydrochloride |
13031-62-4 | 50mg |
$ 187.00 | 2023-09-08 | ||
| TRC | A603001-100mg |
4-Aminobutyramide Hydrochloride |
13031-62-4 | 100mg |
$ 351.00 | 2023-04-19 | ||
| TRC | A603001-250mg |
4-Aminobutyramide Hydrochloride |
13031-62-4 | 250mg |
$ 850.00 | 2023-04-19 | ||
| TRC | A603001-500mg |
4-Aminobutyramide Hydrochloride |
13031-62-4 | 500mg |
$ 1453.00 | 2023-04-19 | ||
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | G276002-50mg |
Gabamide Hydrochloride (4-aminobutanamide hydrochloride) |
13031-62-4 | 50mg |
¥1,380.00 | 2021-05-26 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-IK216-50mg |
4-Aminobutyramide Hydrochloride |
13031-62-4 | 95+% | 50mg |
324.0CNY | 2021-07-10 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-IK216-200mg |
4-Aminobutyramide Hydrochloride |
13031-62-4 | 95+% | 200mg |
961.0CNY | 2021-07-10 |
4-Aminobutyramide Hydrochloride Related Literature
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Norihito Fukui,Keisuke Fujimoto,Hideki Yorimitsu,Atsuhiro Osuka Dalton Trans., 2017,46, 13322-13341
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Chung-Sung Yang,Mong-Shian Shih,Fang-Yi Chang New J. Chem., 2006,30, 729-735
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Thi Thu Tram Nguyen,Thanh Binh Nguyen Org. Biomol. Chem., 2021,19, 6015-6020
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J. Matthew Kurley,Phillip W. Halstenberg,Abbey McAlister,Stephen Raiman,Richard T. Mayes RSC Adv., 2019,9, 25602-25608
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Shaun D. Wong,Edward I. Solomon Dalton Trans., 2014,43, 17567-17577
Additional information on 4-Aminobutyramide Hydrochloride
4-Aminobutyramide Hydrochloride: A Comprehensive Overview
4-Aminobutyramide Hydrochloride, also known by its CAS number CAS No. 13031-62-4, is a compound that has garnered significant attention in the fields of pharmacology and biochemistry. This compound, which belongs to the class of amino acid derivatives, has been extensively studied for its potential applications in drug development and therapeutic interventions. Recent advancements in research have shed light on its unique properties and mechanisms of action, making it a subject of interest for both academia and industry.
The chemical structure of 4-Aminobutyramide Hydrochloride comprises a butyramide backbone with an amino group attached at the fourth carbon position. This structural arrangement imparts distinctive chemical properties, including its ability to interact with various biological systems. Researchers have explored its role in modulating cellular signaling pathways, particularly those involving neurotransmitters and neuromodulators. These findings have implications for treating conditions such as neurological disorders and metabolic diseases.
One of the most promising areas of research involving 4-Aminobutyramide Hydrochloride is its potential as a precursor to gamma-aminobutyric acid (GABA). GABA is a key inhibitory neurotransmitter in the central nervous system, playing a crucial role in regulating neuronal activity. Studies have demonstrated that this compound can be metabolized into GABA under specific physiological conditions, suggesting its utility in managing conditions associated with GABA deficiency, such as anxiety and epilepsy.
In addition to its neuropharmacological applications, 4-Aminobutyramide Hydrochloride has also been investigated for its metabolic effects. Recent studies indicate that it may influence energy metabolism by interacting with enzymes involved in lipid synthesis and degradation. This property has led to explorations into its potential as an adjunct therapy for obesity and related metabolic disorders.
The synthesis of 4-Aminobutyramide Hydrochloride involves a multi-step chemical process that ensures high purity and stability. Researchers have optimized synthetic protocols to enhance yield and minimize byproducts, making it more accessible for large-scale production. The compound's stability under various storage conditions further adds to its suitability for pharmaceutical applications.
From a regulatory standpoint, 4-Aminobutyramide Hydrochloride has undergone rigorous safety assessments to evaluate its toxicity profile. Preclinical studies suggest that it exhibits low toxicity at therapeutic doses, with minimal adverse effects observed in animal models. These findings are encouraging for its progression into clinical trials.
In conclusion, 4-Aminobutyramide Hydrochloride, CAS No. 13031-62-4, represents a versatile compound with diverse applications in medicine and pharmacology. Its ability to influence neurotransmitter systems and metabolic pathways positions it as a valuable tool in addressing a range of health conditions. As research continues to uncover new insights into its mechanisms and therapeutic potential, this compound is poised to play a significant role in future drug development efforts.
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