Trimethylstearylammonium Chloride
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Trimethylstearylammonium Chloride
structure -
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CAS No:
112-03-8
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Formula:
C21H46ClN
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Chemical Name:
Trimethylstearylammonium Chloride
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Synonyms:
TC-8;Octadecy trimethyl ammonium chloride;stearyl trimethyl ammoium chloride;TRIMETHYLSTEARYLAMMONIUM CHLORIDE;Octadecyl Trimethyl Ammonia Chloride;N-Octadecyl-N,N,N-trimethylammonium chloride;TRIMETHYL-OCTADECADRENYLAMMONIUMCHLORIDE;Octadecyl Trimethyl Ammonium Chloride--1831
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CAS No:
Description
PelletsLargeCrystals
PelletsLargeCrystals
Stearyltrimethylammonium chloride is an organic molecular entity.
solid
Trimethylstearylammonium Chloride Basic Attributes
348.06
347.331879
3917847
203-929-1
CZ70647U92
TSCA listed
DTXSID1026902
White
29239000
Characteristics
λ: 225 nm Amax: ≤0.08λ: 260 nm Amax: ≤0.06λ: 280 nm Amax: ≤0.04λ: 340 nm Amax: ≤0.02
0
3.95810
PelletsLargeCrystals
0.91[at 20℃]
80°C
249℃[at 101 325 Pa]
Soluble in water 1.759 mg/L @ 25°C.
0Pa at 25℃
Non flammable
5.5-8.5 (20℃, 0.05% in H2O)
Inert atmosphere,Room Temperature
Safety Information
8
3
Xn
26-36/37/39-37/39-36/37
BT1750000
Xn
Stable. Incompatible with strong oxidizing agents.
P264, P270, P280, P301+P312, P302+P352, P312, P322, P330, P363, P501
20/21/22-36/37/38-21/22
UN1759
|Danger|H302 (91.37%): Harmful if swallowed [Warning Acute toxicity, oral]|P260, P264, P270, P273, P280, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P322, P330, P361, P363, P391, P405, and P501|Aggregated GHS information provided by 265 companies from 17 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|H302: Harmful if swallowed [Warning Acute toxicity, oral]|P260, P264, P270, P280, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P322, P330, P363, P405, and P501|Warning|P264, P270, P280, P301+P312, P302+P352, P312, P322, P330, P363, and P501
Trimethylstearylammonium Chloride Use and Manufacturing
Pass the octadecyl tertiary amine into the autoclave, add an appropriate amount of isopropanol and no reaction medium, and then add a small amount of sodium hydroxide as a catalyst. After replacing the air in the kettle with nitrogen, the temperature was raised to 50°C, and 1% (mass) excess of methyl chloride was introduced. Close the autoclave. React for 4h at 0.5 MPa. The reaction is over. After desalination, dilute with water to the required concentration. The discharging tank is the finished product.
Cationic surfactant, widely used in asphalt emulsification and waterproof coating emulsification, silicone oil emulsification, hair conditioner cosmetic emulsification and conditioning, fabric fiber soft antistatic, organic bentonite modification, protein flocculation and water treatment flocculation in biopharmaceutical industry, glass fiber softness Processing, anti-scorching agent for nylon parachute surface, as well as bactericide and disinfectant.
Surface active agents
Cleaning and furnishing care products
Emulsion (main components are high polymeric and cyclic silicones); forms a protective film to coat split ends; conditioning agent for rinses and shampoos; glazing agent for hair.
All other chemical product and preparation manufacturing|1-Octadecanaminium, N,N,N-trimethyl-, chloride (1:1): ACTIVE
Cosmetics -> Hair conditioning; Preservative
Computed Properties
Molecular Weight:348.0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:17
Exact Mass:347.3318782
Monoisotopic Mass:347.3318782
Heavy Atom Count:23
Complexity:204
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
Drug Function and Efficacy
Conditioning agent, reduces static electricity and improves manageability
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Trimethylstearylammonium Chloride
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