s-Tribromopropane
1,2,3-Tribromopropane
CAS: 96-11-7
Molecular Formula: C3H5Br3
s-Tribromopropane - Names and Identifiers
s-Tribromopropane - Physico-chemical Properties
| Molecular Formula | C3H5Br3 |
| Molar Mass | 280.78 |
| Density | 2.398g/mLat 25°C(lit.) |
| Melting Point | 16-17°C(lit.) |
| Boling Point | 220°C(lit.) |
| Flash Point | 200°F |
| Solubility | H2O: insoluble |
| Vapor Presure | 0.167mmHg at 25°C |
| Merck | 14,9614 |
| BRN | 1732082 |
| Storage Condition | Store below +30°C. |
| Refractive Index | n20/D 1.584(lit.) |
| Physical and Chemical Properties | Boiling Point: 220 Melting Point: 16 - 17 density: 2.398 |
s-Tribromopropane - Risk and Safety
| Hazard Symbols | Xn - Harmful |
| Risk Codes | R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. R36/37/38 - Irritating to eyes, respiratory system and skin. R40 - Limited evidence of a carcinogenic effect R68 - Possible risk of irreversible effects |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S27 - Take off immediately all contaminated clothing. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
| UN IDs | 2810 |
| WGK Germany | 3 |
| RTECS | TZ8300000 |
| TSCA | Yes |
| HS Code | 2903 39 19 |
| Hazard Class | 6.1(b) |
| Packing Group | II |
s-Tribromopropane - Reference Information
| NIST chemical information | information provided by: webbook.nist.gov (external link) |
| EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
| production method | 1. Preparation Method: In the reaction bottle equipped with stirrer, reflux condenser (equipped with calcium chloride drying tube), dropping funnel, thermometer, add allyl bromide (2)182g(1.5mol), ML of dried carbon tetrachloride. The ice-salt bath was cooled to -5 ° C., and 255g(1.6mol) of dry bromine was added dropwise through a dropping funnel. The dropping acceleration was controlled so that the reaction solution rose to 0 ° C., and the addition was completed for about 1.5h. Slowly up to room temperature and continue to stir the reaction for 30min. The solvent was distilled under reduced pressure, and then a fraction of 92 to 93 ° C./1.33KPA was collected to obtain 400g of 1,2, 3-tribromopropane (1) as an almost colorless liquid in a yield of 95%. Note: (1) The allyl bromide is preferably treated before use, and the treatment method is as follows: first, dry with anhydrous calcium chloride, and then carry out distillation, and collect the fraction of 69~72 °c. [1] |
Last Update：2024-04-10 22:29:15
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View History
s-Tribromopropane
3-Isothiazolecarboxamide, 4-amino-5-[[4-(phenylmethyl)-1-piperazinyl]carbonyl]-
(R)-2-((S)-1-(4-(trifluoromethyl)phenethyl)-6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)-N-methyl-2-phenylacetamide hydrochloride
ZINC00258953
ethyl 2-(2-hydroxyphenylamino)acetate
Glycyrrhetinic acid
ethyl 1-(aMinoMethyl)
356783-27-2
(1S,4S)-2-benzyl-2,5-diazabicyclo[2.2.1]heptane-2HCl
3-(2-chlorophenyl)-3-oxo-2-(phenylhydrazono)propanenitrile
3-Isothiazolecarboxamide, 4-amino-5-[[4-(phenylmethyl)-1-piperazinyl]carbonyl]-
(R)-2-((S)-1-(4-(trifluoromethyl)phenethyl)-6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)-N-methyl-2-phenylacetamide hydrochloride
ZINC00258953
ethyl 2-(2-hydroxyphenylamino)acetate
Glycyrrhetinic acid
ethyl 1-(aMinoMethyl)
356783-27-2
(1S,4S)-2-benzyl-2,5-diazabicyclo[2.2.1]heptane-2HCl
3-(2-chlorophenyl)-3-oxo-2-(phenylhydrazono)propanenitrile