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Triethyl Benzyl Ammonium Chloride

Triethyl Benzyl Ammonium Chloride

CAS Number: 56-37-1

Molecular Formula: C13H22N.Cl

Ammonium Compounds (Quaternary)Specialty & Advanced IntermediateToll Manufacturing Phase Transfer CatalystPolymerization Processes TEBACAlkylation Reactions TEBACBenzyltriethylammonium Chloride 99% PurityTEBAC CAS 56-37-1 Supplier

About Triethyl Benzyl Ammonium Chloride

Triethylbenzylammonium Chloride (TEBAC) (CAS 56-37-1) is a premier quaternary ammonium salt that functions as a highly efficient Phase Transfer Catalyst (PTC). TEBAC serves as a vital molecular bridge in biphasic reaction systems, enabling the transport of ionic reagents from an aqueous phase into an organic phase wher...

Synonyms

  • benzyl triethylammonium chloride
  • benzyltriethylammonium
  • Benzyltriethylammonium chloride
  • 56-37-1
  • Benzyl triethylammonium chloride
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Triethyl Benzyl Ammonium Chloride Specifications

CAS Number
56-37-1
Molecular Formula
C13H22N.Cl
Molecular Weight
227.77348
IUPAC Name
benzyl(triethyl)azanium;chloride
Canonical SMILES
CC[N+](CC)(CC)CC1=CC=CC=C1.[Cl-]
InChI Key
HTZCNXWZYVXIMZ-UHFFFAOYSA-M
InChI
1S/C13H22N.ClH/c1-4-14(5-2,6-3)12-13-10-8-7-9-11-13;/h7-11H,4-6,12H2,1-3H3;1H/q+1;/p-1
PubChem CID
66133
EINECS Number
200-270-1
HSN No
292390
Molecular Weight
227.77348
Density
1.08 g/mL at 25°C
Refractive index
n20/D 1.479
Flash Point
>100°C
Appearance
White to off-white crystalline powder
Melting Point
182°C - 186°C (Decomposes)
GHS Hazard Statements
H302 (82.7%): Harmful if swallowed H315 (19.7%): Causes skin irritation H317 (79.2%): May cause an allergic skin reaction H319 (19.2%): Causes serious eye irritation H335 (18.1%): May cause respiratory irritation H412 (78.9%): Harmful to aquatic life with long lasting effects
Precautionary Statement Codes Precautionary Statement Codes
P261, P264, P264+P265, P270, P271, P272, P273, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P333+P317, P337+P317, P362+P364, P403+P233, P405, and P501

API Synthesis

Catalyst in the synthesis of diverse drug classes, particularly in the formation of ethers, esters, and nitriles where reactant solubility is a barrier

Phase Transfer Alkylation

Enables N-alkylation and O-alkylation of sensitive pharmaceutical intermediates without the need for expensive, anhydrous solvents

Reaction Optimization

Reduces reaction times and byproduct formation, leading to cleaner API profiles and easier downstream purification

Herbicide & Pesticide Production

Catalyst in the manufacture of pyrethroid insecticides and various systemic herbicides

Environmental Compliance

Facilitates reactions in aqueous media, reducing the reliance on volatile organic compounds (VOCs) and aligning with sustainable agricultural manufacturing

Powder Coatings

Curing agent and accelerator for epoxy-powder coatings and thermosetting resins

Metallurgical Processing

Within the Metallurgy Chemicals framework, it is utilised in specialised extraction processes and as a surface-active agent in plating baths

Detail 1

Store in a cool, dry area (15-25°C)

Detail 2

Keep containers tightly closed

Detail 3

Highly Hygroscopic, absorbs moisture from the air, which can cause caking and reduce its catalytic potency

Detail 4

Avoid dust inhalation and contact with skin or eyes

  1. benzyl triethylammonium chloride
  2. benzyltriethylammonium
  3. Benzyltriethylammonium chloride
  4. 56-37-1
  5. Benzyl triethylammonium chloride

Triethyl Benzyl Ammonium Chloride FAQs

Minimum Order Quantity

25 kg (evaluation) · 1 MT (commercial)

Lead Time

3 – 5 weeks estimated

Delivery Terms

FOB*

Packaging

20 L pails, 200 L HDPE drums, 1000 L IBC

US Availability

US Facility Inventory

Documentation

US SDS · COA · TDS · Specification sheet

US Regulatory & Quality Information

TSCA status*

US SDS / HazCom*

GHS classification*

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DOT shipping classification*

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California Prop 65*

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