Isopropyl bromoacetate
Isopropyl bromoacetate (CAS: 29921-57-1) is an organic ester compound with a molecular weight of 181.03 g/mol. It functions as a versatile building block in organic synthesis, particularly within the realm of esters and carbonyl compounds. This chemical is utilized in the preparation of more complex molecules, contributing to advancements in chemical research and development.

Organic Synthesis Intermediate
Isopropyl bromoacetate serves as a key intermediate in various organic synthesis pathways. Its reactive bromoacetate moiety facilitates nucleophilic substitution reactions, enabling the formation of diverse carbon-carbon and carbon-heteroatom bonds.
Synthesis of Biaryl Sulphonamide Derivatives
This compound has been documented for its use in the synthesis of specific biaryl sulphonamide derivatives. These complex structures can find applications in medicinal chemistry research.
Building Block for Specialty Chemicals
As a member of the C2 to C5 organic building blocks category, isopropyl bromoacetate is valuable for constructing smaller organic molecules that are further elaborated into fine chemicals and research reagents.
| Molecular weight | 181.03 |
|---|---|
| Linear formula | BrCH2CO2CH(CH3)2 |
| Assay | 99% |
| Boiling point | 59-61 °C/10 mmHg(lit.) |
| Density | 1.399 g/mL at 25 °C(lit.) |
| Refractive index | n20/D 1.444(lit.) |
| Application | Isopropyl bromoacetate has been used in the synthesis of biaryl sulphonamide derivatives1. |

Hazard statements
- H314Causes severe skin burns and eye damage
Precautionary statements
- P280Wear protective gloves, clothing and eye/face protection
- P305IF IN EYES
- P310Immediately call a POISON CENTER or doctor
| Protective equipment | Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter |
|---|---|
| Flash point | 113 °C / 235.4 °F |
| Transport (UN / ADR) | UN 3265 8 / PGII |
| Water hazard class (WGK, DE) | 3 |
| Hazard codes (EU) | C |
| Risk statements (R) | 34 |
| Safety statements (S) | 26-36/37/39-45 |
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 Isopropyl bromoacetate used for?
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Isopropyl bromoacetate is used as an intermediate in organic synthesis, including the preparation of biaryl sulphonamide derivatives and other specialty chemicals.
What are the CAS number and chemical formula for Isopropyl bromoacetate?
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The CAS number for Isopropyl bromoacetate is 29921-57-1. Its linear formula is BrCH2CO2CH(CH3)2.
What grade and purity does Tech Serve Solutions supply?
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Tech Serve Solutions supplies Isopropyl bromoacetate with a purity of 99% (assay). We do not represent this product as USP, BP, or EP grade.
How should Isopropyl bromoacetate be handled safely?
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Isopropyl bromoacetate is classified as Danger, with hazard statement H314 (Causes severe skin burns and eye damage). Appropriate personal protective equipment including gloves, goggles, and faceshields must be worn. In case of inadequate ventilation, a full-face respirator is recommended. Handle with extreme caution.
Is Isopropyl bromoacetate a controlled substance?
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The provided data does not indicate that Isopropyl bromoacetate is a controlled substance.
How is Isopropyl bromoacetate packed, shipped, and exported?
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Isopropyl bromoacetate is packed in accordance with UN 3265, Class 8, Packing Group II regulations for safe transport. TSS exports fine chemicals globally.
How can I request a sample or quote for Isopropyl bromoacetate?
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To request a sample or quote for Isopropyl bromoacetate, please contact our sales department through the TSS website or by telephone.
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