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| Hexadecyl trimethyl ammonium bromide Basic information |
| Hexadecyl trimethyl ammonium bromide Chemical Properties |
Melting point | 248-251 °C(lit.) | density | 1.1107 (rough estimate) | refractive index | 1.5260 (estimate) | Fp | 244 °C | storage temp. | Store below +30°C. | solubility | H2O: 50 mg/mL | form | powder | color | white | Odor | Odorless | PH Range | 5 - 7 | PH | 5.0-7.0 (25℃, 0.1M in H2O) | Water Solubility | 13 g/L (20 ºC) | Sensitive | Hygroscopic | λmax | λ: 260 nm Amax: 0.06 λ: 280 nm Amax: 0.05 | Merck | 14,2025 | BRN | 3598189 | Stability: | Stable. Incompatible with strong oxidizing agents. Protect from moisture. | InChIKey | LZZYPRNAOMGNLH-UHFFFAOYSA-M | CAS DataBase Reference | 57-09-0(CAS DataBase Reference) | EPA Substance Registry System | Cetyl trimethyl ammonium bromide (57-09-0) |
| Hexadecyl trimethyl ammonium bromide Usage And Synthesis |
Chemical Properties | White powder. Soluble in water, alcohol,
and chloroform. | Uses | Hexadecyltrimethylammonium Bromide (CTAB) is a cationic surfactant used as a template in the synthesis of Mesoporous γ-Fe2O3. | Uses | antiinfectant | Uses | cetrimonium bromide is a quaternary ammonium salt that can prevent the proliferation of bacteria, fungi, and yeast in cosmetic preparation, while also act as an emulsifying agent. | Uses | A cationic detergent used in the isolation of high molecular weight DNA. | Definition | ChEBI: The organic bromide salt that is the bromide salt of cetyltrimethylammonium; one of the components of the topical antiseptic cetrimide. | General Description | Hexadecyltrimethylammonium bromide is a titrant for the potentiometric titration of perchlorate with ionselective electrodes. | Biochem/physiol Actions | Hexadecyltrimethylammonium bromide also called cetyltrimethylammonium bromide (CTAB), is a cationic surfactant. CTAB is employed for extraction of DNA. CTAB method is efficient, cost and time effective for DNA extraction. CTAB is used as a shaping material and reducing agent for nanoparticle generation. | Purification Methods | Crystallise it from EtOH, EtOH/*benzene or from wet acetone after extracting twice with pet ether. Shake it with anhydrous diethyl ether, filter and dissolve it in a little hot MeOH. After cooling in the refrigerator, the precipitate is filtered off at room temperature and re-dissolved in MeOH. Anhydrous ether is added and, after warming to obtain a clear solution, it is cooled and the crystalline material is collected. [Dearden & Wooley J Phys Chem 91 2404 1987, Hakemi et al. J Am Chem Soc 91 120 1987, Beilstein 4 IV 819.] | References | [1] Liu, Tingting et al. “Hexadecyl trimethyl ammonium bromide assisted growth of NiCo2O4@reduced graphene oxide/ nickel foam nanoneedle arrays with enhanced performance for supercapacitor electrodes?.” RSC Advances 7 (2022): 4029–4041. |
| Hexadecyl trimethyl ammonium bromide Preparation Products And Raw materials |
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