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4-Isopropylbenzoic acid, 98%|589682|536-66-3

4-Isopropylbenzoic acid, 98%

Cat. No JK589682_25_G
J&K Chemical

Product Information

Product Name
4-Isopropylbenzoic acid, 98%
Brand Name
J&K
Product Number
589682
CAS
536-66-3
Molecular Formula
C10H12O2
Molecular Weight
164.20
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
Cuminic acid
PubChem CID
10820
IUPAC Name
4-propan-2-ylbenzoic acid
InChI Key
CKMXAIVXVKGGFM-UHFFFAOYSA-N
SMILES
CC(C)C1=CC=C(C=C1)C(=O)O

Properties

Melting Point
117-120

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H302
H312
H315
H319
H332
H335
Precautionary Statement
P270
P330
P501
P280
P321
P261
P271
P319
P405
P301+P317
P302+P352
P362+P364
P332+P317
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References

A rapid and efficient strategy for combinatorial repression of multiple genes in Escherichia coli
Publication Name: Microbial Cell Factories
Publication Date: 2025-03-28
DOI: 10.1186/s12934-025-02697-x

De novo design of ribosomally synthesized and post-translationally modified peptides
Publication Name: Nature Chemistry
Publication Date: 2025-01-07
DOI: 10.1038/s41557-024-01685-9

Programmable trans-splicing riboregulators for complex cellular logic computation
Publication Name: Nature Chemical Biology
Publication Date: 2025-01-02
DOI: 10.1038/s41589-024-01781-4

Fungal Phytopathogens as a Source of Metabolites for Agricultural Applications
Publication Name: Fungal Metabolites for Agricultural Applications
Publication Date: 2025
DOI: 10.1007/978-3-031-76587-2_13

Dynamic control of the plasmid copy number maintained without antibiotics in Escherichia coli
Publication Name: Journal of Biological Engineering
Publication Date: 2024-12-19
DOI: 10.1186/s13036-024-00460-1

4-Isopropylbenzoic acid, 98%

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