(S)-(−)-N-(Trifluoroacetyl)pyrrolidine-2-carbonyl chloride solution
(S)-(−)-N-(Trifluoroacetyl)pyrrolidine-2-carbonyl chloride solution (CAS: 36724-68-2; C7H7ClF3NO2; MW: 229.58) is a chiral acid halide. Supplied as a 0.1 M solution in methylene chloride, this compound is primarily utilised as a derivatizing agent. Its high optical purity (ee: 97%) makes it suitable for gas chromatographic analysis of chiral amines and alcohols, aiding in enantiomeric separation and quantification.
- IUPAC
- (S)-(−)-N-(Trifluoroacetyl)prolyl chloride solution,TPC

Chiral Derivatization Agent
This compound serves as a derivatizing agent for the gas chromatographic (GC) assay of chiral amines and alcohols. It reacts with these analytes to form derivatives that are more volatile and readily separated on a chiral GC column.
Asymmetric Synthesis
As a chiral building block, it can be employed in asymmetric synthesis to introduce stereochemistry into target molecules. Its trifluoroacetyl group can also serve as a protecting or activating group in synthetic pathways.
GC Analysis of Enantiomers
The high optical purity (ee: 97%) makes it particularly useful for the enantioselective analysis of chiral compounds by GC, enabling accurate determination of enantiomeric excess.
| Molecular weight | 229.58 |
|---|---|
| Empirical formula | C7H7ClF3NO2 |
| Density | 1.308 g/mL at 25 °C |
| Refractive index | n20/D 1.424 |
| Concentration | 0.1 M in methylene chloride |
| Optical purity | ee: 97% (GLC) |
| Storage temperature | 2-8°C |
| Application | Derivatizing agent for the GC assay of chiral amines and alcohols. |

Hazard statements
- H351Suspected of causing cancer
Precautionary statements
- P281Use personal protective equipment as required
| Protective equipment | Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter |
|---|---|
| Transport (UN / ADR) | UN 1593 6.1 / PGIII |
| Water hazard class (WGK, DE) | 2 |
| Hazard codes (EU) | Xn |
| Risk statements (R) | 40 |
| Safety statements (S) | 36/37 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is (S)-(−)-N-(Trifluoroacetyl)pyrrolidine-2-carbonyl chloride solution used for?
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(S)-(−)-N-(Trifluoroacetyl)pyrrolidine-2-carbonyl chloride solution is primarily used as a derivatizing agent for the gas chromatographic assay of chiral amines and alcohols, aiding in their enantiomeric separation and quantification.
What are the CAS number and chemical formula?
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The CAS number is 36724-68-2, and the molecular formula is C7H7ClF3NO2.
What grade and purity does Tech Serve Solutions supply?
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Tech Serve Solutions supplies this product with a reported optical purity of ee: 97% (GLC) and as a 0.1 M solution in methylene chloride. We do not represent this product as USP, BP, EP or other pharmacopoeial grades.
What are the safety and handling considerations?
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This compound is classified under GHS08 with a 'Warning' signal word, and carries the hazard statement H351 (Suspected of causing cancer). Appropriate personal protective equipment, including eyeshields, faceshields, gloves, and respiratory protection (e.g., multi-purpose combination respirator cartridge or AB EK type filter), is required. It is classified as WGK 2 in Germany and requires storage at 2-8°C.
How is this product shipped and exported?
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This chemical is shipped and exported under UN 1593, hazard class 6.1, packing group III.
How can I request a sample or quote?
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To request a sample or a quote for (S)-(−)-N-(Trifluoroacetyl)pyrrolidine-2-carbonyl chloride solution, please contact our sales department via the website or your dedicated account manager.
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