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Acetylcholine chloride, 98+%
CAS: 60-31-1 | C7H16ClNO2 | 181.66 g/mol
$112.62 - $319.52
Chemical Identifiers
| CAS | 60-31-1 |
|---|---|
| Molecular Formula | C7H16ClNO2 |
| Molecular Weight (g/mol) | 181.66 |
| MDL Number | MFCD00011698 |
| InChI Key | JUGOREOARAHOCO-UHFFFAOYSA-M |
| Synonym | acetylcholine chloride, miochol, acecoline, chloroacetylcholine, arterocoline, acecholin, ovisot, ach chloride, azetylcholinchlorid, 2-acetyloxy-n,n,n-trimethylethanaminium chloride |
| PubChem CID | 6060 |
| ChEBI | CHEBI:2417 |
| IUPAC Name | 2-acetyloxyethyl(trimethyl)azanium;chloride |
| SMILES | CC(=O)OCC[N+](C)(C)C.[Cl-] |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAL0216814
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Thermo Scientific Chemicals
L0216814 |
25 g |
Each for $112.62
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AAL0216822
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Thermo Scientific Chemicals
L0216822 |
100 g |
Each for $319.52
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Description
Acetylcholine chloride acts as an endogenous neurotransmitter at cholinergic synapses. The compound has been shown to have ophthalmological uses and can be broken down quickly by choliesterases. Acetylcholine influences many basic cells functions, such as mitosis, cells differentiation, cytoskeletal organization, and cell to cell contact, among other functions. It reduces mortality and plasma proinflammatory cytokines in mice with experimentally-induced sepsis.The cholinergicanti-infl ammatory mechanism is probably mediated by interaction of acetylcholine with α7n cholinoreceptor on monocytes, macrophages, and neutrophils, which decreases the levels of proinflammatory cytokines such as TNF-α, IL-1β, and IL-6.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
ApplicationsAcetylcholine chloride acts as an endogenous neurotransmitter at cholinergic synapses. The compound has been shown to have ophthalmological uses and can be broken down quickly by choliesterases. Acetylcholine influences many basic cells functions, such as mitosis, cells differentiation, cytoskeletal organization, and cell to cell contact, among other functions. It reduces mortality and plasma proinflammatory cytokines in mice with experimentally-induced sepsis.The cholinergicanti-infl ammatory mechanism is probably mediated by interaction of acetylcholine with α7n cholinoreceptor on monocytes, macrophages, and neutrophils, which decreases the levels of proinflammatory cytokines such as TNF-α, IL-1β, and IL-6.
Solubility
Soluble in water (600 g/L at 20°C), alcohol, DMSO (36 mg/ml at 25°C), and ethanol (36 mg/ml at 25°C). Insoluble in ether.
Notes
Store away from moisture. Store under dry inert gas. Incompatible with heat,oxidizing agents.
Chemical Identifiers
| 60-31-1 | |
| 181.66 | |
| JUGOREOARAHOCO-UHFFFAOYSA-M | |
| 6060 | |
| 2-acetyloxyethyl(trimethyl)azanium;chloride |
| C7H16ClNO2 | |
| MFCD00011698 | |
| acetylcholine chloride, miochol, acecoline, chloroacetylcholine, arterocoline, acecholin, ovisot, ach chloride, azetylcholinchlorid, 2-acetyloxy-n,n,n-trimethylethanaminium chloride | |
| CHEBI:2417 | |
| CC(=O)OCC[N+](C)(C)C.[Cl-] |
Specifications
| 60-31-1 | |
| C7H16ClNO2 | |
| 25 g | |
| Very Hygroscopic | |
| acetylcholine chloride, miochol, acecoline, chloroacetylcholine, arterocoline, acecholin, ovisot, ach chloride, azetylcholinchlorid, 2-acetyloxy-n,n,n-trimethylethanaminium chloride | |
| JUGOREOARAHOCO-UHFFFAOYSA-M | |
| 2-acetyloxyethyl(trimethyl)azanium;chloride | |
| 6060 | |
| 181.66 | |
| Acetylcholine chloride |
| 149°C to 152°C | |
| MFCD00011698 | |
| 3571875 | |
| 14,87 | |
| Soluble in water (600g/L at 20°C),alcohol,DMSO (36mg/ml at 25°C),and ethanol (36mg/ml at 25°C). Insoluble in ether. | |
| CC(=O)OCC[N+](C)(C)C.[Cl-] | |
| 181.66 | |
| CHEBI:2417 | |
| ≥98% |
Safety and Handling
GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
H315-H319-H335
EINECSNumber : 200-468-8
RTECSNumber : FZ9800000
TSCA : Yes
Recommended Storage : Keep cold; Store under Argon
RUO – Research Use Only