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ACETYLCHOLINE IODIDE

CAS No.
2260-50-6
Chemical Name:
ACETYLCHOLINE IODIDE
Synonyms
ACH;CEK2;JTK4;CD333;HSFGFR3EX;acetylcolina;CD333 antigen;acetyl-choliniodide;Acetylholine iodide;Acetycholine iodide
CBNumber:
CB4131593
Molecular Formula:
C7H16INO2
Molecular Weight:
273.11
MDL Number:
MFCD00011815
MOL File:
2260-50-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-24 12:01:10
Product description Number Pack Size Price
FGFR3 (K650E), active, GST tagged human PRECISIO®, recombinant, expressed in baculovirus infected Sf9 cells, ≥70% (SDS-PAGE), buffered aqueous glycerol solution SRP5301 10 μg $430
Anti-FGFR3 antibody produced in rabbit affinity isolated antibody SAB4500888 100 μg $560
Anti-FGFR3 antibody produced in rabbit affinity isolated antibody SAB3501041 100μG $569
FGFR3 (397-end), active, GST tagged human PRECISIO? Kinase, recombinant, expressed in baculovirus infected Sf9 cells, ≥70% (SDS-PAGE), buffered aqueous glycerol solution F7930 10μg $576
Acetylcholine iodide ≥97% A7000 5g $68
More product size

ACETYLCHOLINE IODIDE Properties

Melting point 161-164 °C
Density 1.4816 (estimate)
storage temp. -20°C
solubility Soluble in DMSO
form Crystalline Powder
color White
biological source rabbit
Water Solubility almost transparency
Sensitive Light Sensitive & Hygroscopic
Specific Activity 95-129nmol/min·mg
BRN 3571339
InChI 1S/C7H16NO2.HI/c1-7(9)10-6-5-8(2,3)4;/h5-6H2,1-4H3;1H/q+1;/p-1
InChIKey SMBBQHHYSLHDHF-UHFFFAOYSA-M
SMILES [I-].CC(=O)OCC[N+](C)(C)C
CAS DataBase Reference 2260-50-6(CAS DataBase Reference)
FDA UNII 7ZCP12S7HQ
EPA Substance Registry System Ethanaminium, 2-(acetyloxy)-N,N,N-trimethyl-, iodide (2260-50-6)
UNSPSC Code 51111800
NACRES NA.41

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
target organs Respiratory system
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
RTECS  KH3300000
8-9
TSCA  TSCA listed
HS Code  29239000
Storage Class 11 - Combustible Solids
Hazard Classifications Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
NFPA 704
1
2 1

ACETYLCHOLINE IODIDE price More Price(32)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SRP5301 FGFR3 (K650E), active, GST tagged human PRECISIO®, recombinant, expressed in baculovirus infected Sf9 cells, ≥70% (SDS-PAGE), buffered aqueous glycerol solution 10 μg $430 2026-04-30 Buy
Sigma-Aldrich SAB4500888 Anti-FGFR3 antibody produced in rabbit affinity isolated antibody 100 μg $560 2026-04-30 Buy
Sigma-Aldrich SAB3501041 Anti-FGFR3 antibody produced in rabbit affinity isolated antibody 100μG $569 2026-04-30 Buy
Sigma-Aldrich F7930 FGFR3 (397-end), active, GST tagged human PRECISIO? Kinase, recombinant, expressed in baculovirus infected Sf9 cells, ≥70% (SDS-PAGE), buffered aqueous glycerol solution 2260-50-6 10μg $576 2026-04-30 Buy
Sigma-Aldrich A7000 Acetylcholine iodide ≥97% 2260-50-6 5g $68 2026-04-30 Buy
Product number Packaging Price Buy
SRP5301 10 μg $430 Buy
SAB4500888 100 μg $560 Buy
SAB3501041 100μG $569 Buy
F7930 10μg $576 Buy
A7000 5g $68 Buy

ACETYLCHOLINE IODIDE Chemical Properties,Uses,Production

Chemical Properties

WHITE CRYSTALLINE POWDER

Uses

Acetylcholine is an endogenous neurotransmitter at cholinergic synapses that amplifies action potential of the sarcolemma thereby inducing muscle contractions. Acetylcholine iodide is used as an acetylcholine receptor agonist to identify, characterize and differentiate among types of cholinergic receptors. Acetylcholine iodide is used as a substrate to identify and characterize natural and mutated acetylcholinesterase(s).

Biochem/physiol Actions

Endogenous neurotransmitter at cholinergic synapses; amplifies action potential of the sarcolemma thereby inducing muscle contractions.

Synthesis

3,5-DIHYDROXY-4-ACETYLTOLUENE

1634-34-0

CHOLINE IODIDE

17773-10-3

ACETYLCHOLINE IODIDE

2260-50-6

General procedure for the synthesis of 2-acetoxy-N,N,N-trimethylethane-1-ammonium iodide from 3,5-dihydroxy-4-acetyltoluene and (2-hydroxyethyl)trimethylammonium iodide: 3 moles of 3,5-dihydroxy-4-acetyltoluene and 5 moles of (2-hydroxyethyl)trimethylammonium iodide were added to a reaction vessel with controlled stirring at a speed of 130 rpm, and the temperature was raised to 65 °C. The temperature was increased to 65 °C. The temperature was maintained with continuous stirring until the reactants were completely dissolved. Subsequently, the reaction mixture was allowed to stand for 120 minutes. The temperature of the solution was lowered to 15 °C to promote crystal precipitation, followed by filtration. The crystals were washed with 85% cyclohexane solution, followed by washing again with 90% toluene solution. Finally, dehydration was carried out using anhydrous potassium carbonate as dehydrating agent to afford 761.67 g of 2-acetoxy-N,N,N-trimethylethane-1-ammonium iodide in 93% yield.

in vivo

Acetylcholine iodide (3 μg; i.v.) increases the electrical potential difference in the proximal colon of rats[2].
Acetylcholine iodide (25 mg/kg; subcutaneous injection; twice a day; 15 days) induces mammary ductal growth in some virgin rats[3].
Acetylcholine iodide (25 mg/kg; subcutaneous injection; twice a day; 5 days) induces lobular-acinar growth and secretion in the mammary glands of virgin rats pretreated with estrogen[3].

Animal Model:Female albino rats (Carworth, weighing 175 - 200 g, age unspecified) for studying mammary growth and lactation induction; Female albino rats (Carworth, postparturient, litter removed on 4th day after parturition) for studying maintenance of mammary structure and secretion[3].
Dosage:25 mg/kg, 50 mg/kg (dissolved in an unspecified solvent for subcutaneous injection)
Administration:Subcutaneous injection, twice daily for 15 days (for induction in virgin rats), twice daily for 5 days after 10 days of estradiol pretreatment (for induction in estrogen-primed virgin rats), twice daily for 10 days (for maintenance in lactating rats after litter removal)
Result:Induced duct growth in some cases without estradiol priming, and lobule-alveolar growth and secretion with estradiol priming in virgin rats.
Retarded mammary involution and maintained lactation in lactating rats after litter removal.

IC 50

Human Endogenous Metabolite

References

[1] Patent: CN108250089, 2018, A. Location in patent: Paragraph 0011; 0013; 0015

ACETYLCHOLINE IODIDE Preparation Products And Raw materials

Global( 194)Suppliers
Supplier Tel Email Country ProdList Advantage
career henan chemical co
+86-0371-86658258 +8613203830695 factory@coreychem.com China 29794 58
TargetMol Chemicals Inc.
+1-781-999-5354; +17819995354 marketing@targetmol.com United States 32467 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +8618949823763 sales@tnjchem.com China 34563 58
Dayang Chem (Hangzhou) Co.,Ltd.
+86-0571-88938639 +8617705817739 info@dycnchem.com China 52705 58
TargetMol Chemicals Inc.
+1-781-999-5354; support@targetmol.com United States 39040 58
PT CHEM GROUP LIMITED
+86-85511178; peter68@ptchemgroup.com China 35425 58
GIHI CHEMICALS CO.,LIMITED
+86-571-86217390; +8618058761490 info@gihichemicals.com China 49967 58
SUZHOU SENFEIDA CHEMICAL CO.,LTD
+86-0512-83500002 +8618662433356 3899766280@qq.com China 26362 58
Shanghai Acmec Biochemical Technology Co., Ltd.
+86-18621343501; +undefined18621343501 product@acmec-e.com China 33324 58
Aladdin Scientific
tp@aladdinsci.com United States 57505 58

View Lastest Price from ACETYLCHOLINE IODIDE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Acetylcholine iodide pictures 2026-04-23 Acetylcholine iodide
2260-50-6
US $41.00-93.00 / mg 99.86% 10g TargetMol Chemicals Inc.
ACETYLCHOLINE IODIDE pictures 2020-02-14 ACETYLCHOLINE IODIDE
2260-50-6
US $7.00 / KG 1KG 99% 100kg Career Henan Chemical Co
N-(2-HYDROXYETHYL)TRIMETHYLAMMONIUM IODIDE ACETATE ACH ACETYLCHOLINE IODIDE 2-(acetyloxy)-n,n,n-trimethyl-ethanamiuiodide Acetylcholine iodide;(2-Acetoxyethyl)-trimethyammoniumiodide ACETYLCHOLINE IODIDE CRYSTALLINE O-AcetylcholineIodide 2-(ACETYLOXY)-N,N,N-TRIMETHYLETHANAMINIUM IODIDE 2-ACETOXYETHYLTRIMETHYLAMMONIUM IODIDE Acetylcholine iodide,99% 2-(Dimethylamino)ethyl acetate methiodide Acetylchloineiodide 2-acetoxy-N,N,N-triMethylethanaMiniuM iodide Anti-FGFR3 (C-terminal) antibody produced in rabbit 2-acetyloxyethyl(trimethyl)azanium,iodide 2-(acetyloxy)-n,n,n-trimethylethanamiumiodide acetyl-choliniodide acetylcolina Anti-FGFR3 antibody produced in rabbit CEK2 FGFR3 (397-end), active, GST tagged human HSFGFR3EX JTK4 FGFR3 (K650E), active, GST tagged human Acetylholine iodide choline,iodide,acetate(ester) cholineacetate(ester),iodide (2-Hydroxyethyl)-trimethylammonium iodide acetate Acetycholine iodide (2-Acetoxyethyl)-trimethyammoniumiodide AcetylcholineIodide> ACETYLCHOLINE IODIDE FOR SYNTHESIS Acetylcholine iodide, GR 99% Acetylcholine Iodide extrapure, 99% 2-Acetoxy-N,N,N-trimethylethan-1-aminium iodide Acetyl Choline Iodide 99% AR Acetylcholine iodide, 10 mM in DMSO CD333 antigen CD333 2260-50-6 CH3CO2CH2CH2NCH33I CH33NICH2CH2OCOCH3 C7H16INO2 C7H16NO2I Quaternary Ammonium Compounds Ammonium Iodides (Quaternary) Phase Transfer Catalysts Synthetic Reagents Ammonium Salts Substrates Ammonium Iodides (Quaternary) Quaternary Ammonium Compounds