Cas no 301-02-0 (Oleamide)
Oleamide Chemical and Physical Properties
Names and Identifiers
-
- Oleamide
- SLEEPAMIDE
- ODA
- OLEYRAMIDE
- OLEYLAMIDE
- (9Z)-9-Octadecenamide
- (Z)-9-Octadecenamide
- 9-Octadecenamide,(Z)-
- cis-90010-Octadecenamide
- Adogen 73
- AMD-O
- Amide O
- Armid O
- cis-9,10-Octadecenoamide
- cis-9,10-Octadecenoamide cis-9-Octadecenamide Oleic acid amide
- cis-9-octadecenamide
- OctadecyldiMethyltriMethoxysilylpropylaMMoniuMchlorideinMe
- OLEAMID
- Oleic acid amide
- oleicacidamide-heptaglycolether
- Plastic additive 20
- Slip-eze
- Oleamide R
- cis-9-Octadecenoamide
- Oleyl amide
- Crodamide O
- Armoslip CP
- Crodamide OR
- (9Z)-octadec-9-enamide
- 9-Octadecenamide, (Z)-
- 9-Octadecenamide
- (Z)-octadec-9-enamide
- ELAIDOYLAMIDE
- 9Z-octadecenamide
- 9,10-octadecenamide
- Unislip 1759
- 9-Octadecenamide, (9Z)-
- Kemamide O
- Petrac Slip-Eze
- Diamide O 200
- 14C-labeled oleamide
- 9,10-octadecenoamide
- HSD
- (9Z)-octadecenamide
- (Z)-Octadec-9-enoic acid amide
- Oleamide,70%
- 2,2'-Dibromobiphenyl
-
- MDL： MFCD00053638
- Inchi： 1S/C18H35NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h9-10H,2-8,11-17H2,1H3,(H2,19,20)/b10-9-
- InChI Key： FATBGEAMYMYZAF-KTKRTIGZSA-N
- SMILES： O=C(C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C(/[H])=C(/[H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H])N([H])[H]
Computed Properties
- Exact Mass: 281.27200
- Monoisotopic Mass: 281.271865
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 20
- Rotatable Bond Count: 15
- Complexity: 236
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 1
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 43.1
- XLogP3: 7.464
Experimental Properties
- Color/Form: This product is white powder or flake.
- Density: 0.8790
- Melting Point: 65.0 to 75.0 deg-C
- Boiling Point: 433.3 °C at 760 mmHg
- Flash Point: 215.9 °C
- Refractive Index: 1.468
- PSA: 43.09000
- LogP: 6.20950
- Solubility: Insoluble in water, soluble in ether and ethanol.
Oleamide Security Information
-
Symbol:
- Signal Word：Warning
- Hazard Statement： H315,H317,H319,H335
- Warning Statement： P261,P280,P305+P351+P338
- Hazardous Material transportation number：NONH for all modes of transport
- WGK Germany：1
- Hazard Category Code： 36/37/38-43
- Safety Instruction： S26-S36
- RTECS：RG2230000
-
Hazardous Material Identification：
- Storage Condition：Please store the product under the recommended conditions in the Certificate of Analysis.
- Safety Term：S26;S36
- Risk Phrases：R36/37/38
Oleamide Customs Data
- HS CODE：2924199090
- Customs Data：
China Customs Code:
2924199090Overview:
2924199090. Other acyclic amides(Including acyclic carbamates)(Including its derivatives and salts). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%
Declaration elements:
Product Name, component content, use to, packing
Summary:
2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
Oleamide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Fluorochem | M02209-1g |
cis-9,10-Octadecanamide |
301-02-0 | 65% | 1g |
￡10.00 | 2021-07-01 | |
| Fluorochem | M02209-25g |
cis-9,10-Octadecanamide |
301-02-0 | 65% | 25g |
￡17.00 | 2022-02-28 | |
| Fluorochem | M02209-500g |
cis-9,10-Octadecanamide |
301-02-0 | 65% | 500g |
￡53.00 | 2022-02-28 | |
| SHANG HAI XIANG HUI YI YAO Technology Co., Ltd. | CB04011-25g |
Oleamide |
301-02-0 | 97% | 25g |
53.00 | 2021-07-09 | |
| TRC | O255000-50mg |
Oleamide |
301-02-0 | 50mg |
80.00 | 2021-07-22 | ||
| TRC | O255000-100mg |
Oleamide |
301-02-0 | 100mg |
100.00 | 2021-07-22 | ||
| TRC | O255000-250mg |
Oleamide |
301-02-0 | 250mg |
145.00 | 2021-07-22 | ||
| TRC | O255000-500mg |
Oleamide |
301-02-0 | 500mg |
295.00 | 2021-07-22 | ||
| TRC | O255000-1g |
Oleamide |
301-02-0 | 1g |
435.00 | 2021-07-22 | ||
| TRC | O255000-2.5g |
Oleamide |
301-02-0 | 2.5g |
565.00 | 2021-07-22 |
Oleamide Suppliers
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Oleamide Related Literature
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Saayak Halder,Nathaniel J. Macatangay,Breanna L. Zerfas,Andres F. Salazar-Chaparro,Darci J. Trader RSC Med. Chem. 2022 13 1077
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Wenfeng Zhang,Haitao Wang,Boxue Chen,Xianghong Bi,Swaminathan Venkatesan,Qiquan Qiao,Shangfeng Yang J. Mater. Chem. 2012 22 24067
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Zejun Yu,Dong Li,Shengbing Zhai,Hang Xu,Hao Liu,Mingzhang Ao,Chunfang Zhao,Wenwen Jin,Longjiang Yu Food Funct. 2021 12 9211
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Wenbin Niu,Suli Wu,Shufen Zhang J. Mater. Chem. 2010 20 9113
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Melany P. Puglisi,Jennifer M. Sneed,Koty H. Sharp,Raphael Ritson-Williams,Valerie J. Paul Nat. Prod. Rep. 2014 31 1510
Additional information on Oleamide
Professional Introduction to Oleamide (CAS No. 301-02-0)
Oleamide, with the chemical formula C9H17NO2 and the CAS number 301-02-0, is a significant compound in the field of chemical and pharmaceutical research. This linear amide derived from oleic acid has garnered considerable attention due to its diverse applications and potential therapeutic benefits. In recent years, advancements in biochemical studies have highlighted the multifaceted roles of Oleamide in various biological processes, making it a subject of intense interest among researchers.
The molecular structure of Oleamide consists of a saturated hydrocarbon chain with an amide functional group, which contributes to its unique chemical properties. This structure allows it to interact with biological targets in multiple ways, making it a versatile compound for drug development. The long hydrocarbon tail enhances its solubility in lipids, facilitating its penetration into cellular membranes, which is crucial for many pharmacological applications.
Recent studies have demonstrated the potential of Oleamide as an endocannabinoid receptor modulator. Endocannabinoids play a pivotal role in regulating pain perception, mood, and appetite. Research indicates that Oleamide can interact with CB1 and CB2 receptors, potentially offering therapeutic benefits in managing chronic pain conditions. This interaction has sparked interest in developing novel analgesics that leverage the properties of Oleamide.
In addition to its role as a cannabinoid receptor modulator, Oleamide has been explored for its effects on neurotransmitter systems. Preclinical studies suggest that it may influence the release and reuptake of serotonin and dopamine, which are key neurotransmitters involved in mood regulation and cognitive functions. These findings open up possibilities for using Oleamide in the treatment of depression and anxiety disorders.
The compound's anti-inflammatory properties have also been a focus of recent research. Chronic inflammation is associated with various diseases, including arthritis and metabolic syndrome. Studies have shown that Oleamide can suppress inflammatory pathways by inhibiting key enzymes such as COX-2 and NF-κB. This makes it a promising candidate for developing anti-inflammatory drugs with fewer side effects compared to traditional NSAIDs.
Beyond its pharmacological applications, Oleamide has found utility in industrial applications as well. Its lubricating properties make it suitable for use in cosmetic formulations and as an additive in skincare products. The ability of Oleamide to enhance skin penetration has also been exploited in transdermal drug delivery systems, improving the efficacy of topical medications.
The synthesis of Oleamide typically involves the reaction between oleic acid or its derivatives with ammonia or ammonium hydroxide under controlled conditions. Advances in synthetic chemistry have enabled more efficient and scalable production methods, making it more accessible for research and commercial purposes. The purity and quality of synthesized Oleamide are critical for ensuring its efficacy in biological assays and pharmaceutical formulations.
The safety profile of Oleamide has been extensively evaluated through toxicological studies. These studies have shown that it exhibits low toxicity at therapeutic doses, making it a relatively safe compound for human use. However, as with any chemical substance, proper handling and storage are essential to prevent any potential adverse effects.
In conclusion, Oleamide (CAS No. 301-02-0) is a multifunctional compound with significant potential in both pharmaceutical and industrial applications. Its ability to modulate endocannabinoid receptors, influence neurotransmitter systems, and exhibit anti-inflammatory properties makes it a valuable candidate for developing new drugs targeting various diseases. Furthermore, its utility in cosmetic formulations highlights its versatility beyond the pharmaceutical domain. As research continues to uncover new applications of this compound, its importance is expected to grow further.
