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10035-10-6 - Hydrogen bromide, 33% w/w (45% w/v) soln. in acetic acid - Hydrobromic acid acetic acid solution - A14475 - Alfa Aesar

A14475 Hydrogen bromide, 33% w/w (45% w/v) soln. in acetic acid

Numéro CAS
10035-10-6
Synonymes
Hydrobromic acid acetic acid solution

Dimensions Prix ($) Quantité Disponibilité
100ml 29,97
500ml 102,60
2500ml 398,70
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Hydrogen bromide, 33% w/w (45% w/v) soln. in acetic acid

MDL
MFCD00011323
EINECS
233-113-0

Propriétés chimiques

Formule
BrH
Poids formulaire
80.92
Point d'éclair
65°(149°F)
Densité
1.40
Solubilité
Miscible with water, alcohol and organic solvents.

Applications

Hydrobromic acid is an indispensable raw material for organic intermediates, inorganic pharmaceuticals, photosensitive materials, dyes and medicines. It is also used in the production of bromine compounds. It is used as an important agent in the industrial processes of isomerization, polymerization, hydration and dehydration and esterification reactions. It plays an essential role for the extraction of mercury from the cinnebar ore.

Notes

Air and light sensitive. Incompatible with strong bases, strong oxidizing agents, ammonia, ozone, fluorine, potassium permanganate, amines, alcohols and metals.

Références bibliographiques

Preferred reagent for the non-hydrogenolytic cleavage of the N-benzyloxycarbonyl (Cbz, Z) group in peptide synthesis: J. Org. Chem., 17, 1564 (1952). For peptide reagents, see Appendix 6.

Used in combination with Paraformaldehyde, A11313, or 1,3,5-Trioxane, A15639, for the bromomethylation of aromatics: J. Org. Chem., 58, 1262 (1993); Synlett, 55 (1989). For N-bromomethylation of phthalimide and other imides, see: Synlett, 933 (1994).

For use in the bromoacetoxylation of (S)-(+)-1,2-Propanediol, B21773, as an example of the conversion of chiral vic-diols to epoxides with retention of configuration, see: J. Chem. Soc., Perkin 1, 1214 (1973); Org. Synth. Coll., 7, 356 (1990).

Cai, X.; Li, Y.; Yue, D.; Yi, Q.; Li, S.; Shi, D.; Gu, Z. Reversible PEGylation and Schiff-base linked imidazole modification of polylysine for high-performance gene delivery. J. Mater. Chem. B 2015, 3 (8), 1507-1517.

Wang, Q. M.; Gao, Z.; Liu, S.; Fan, B.; Kang, L.; Huang, W.; Jin, M. Hybrid polymeric micelles based on bioactive polypeptides as pH-responsive delivery systems against melanoma. Biomaterials 2014, 35 (25), 7008-7021.

Mentions de danger et de prudence du SGH

Mentions de danger (UE): H314-H335-H227

Causes severe skin burns and eye damage. May cause respiratory irritation. Combustible liquid.

Mentions de prudence: P210-P260-P261-P280-P303+P361+P353-P305+P351+P338-P301+P330+P331-P304+P340-P405-P501a

Keep away from heat/sparks/open flames/hot surfaces. - No smoking. Do not breathe dust/fume/gas/mist/vapours/spray. Avoid breathing dust/fume/gas/mist/vapours/spray. Wear protective gloves/protective clothing/eye protection/face protection. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.

Autres références

Merck
14,4778
Beilstein
3587158
Classe de danger
8
Groupe d'emballage
II
Code tarifaire harmonisé
2811.19
TSCA
Yes
RTECS
MW3850000

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