Detail of > 106-94-5
- MSDS Download

- CAS Number:
- 106-94-5
- Name:
1-Bromopropane
- Formula:
- C3H7Br
- Molecular Structure:

- Synonyms:
- 1-Propyl bromide;Ascusol MC;Drysolv;Leksol;Propyl bromide;n-Propyl bromide;
- Molecular Weight:
- 123.01
- EINECS:
- 203-445-0
- Density:
- 1.348 g/cm3
- Melting Point:
- -110 °C
- Boiling Point:
- 71.7 °C at 760 mmHg
- Flash Point:
- 25.6 °C
- Solubility:
- 2.5 g/L (20 °C) in water
- Appearance:
- Colorless transparent liquid
- Hazard Symbols:
F,
T- Risk Codes:
- 60-11-36/37/38-48/20-63-67
- Safety:
- 53-45Details
- Transport Information:
- UN 2344 3/PG 2
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Reference
- Distribution and excretion of alkyl bromides from the body
- Distribution and excretion of alkyl bromides from the body. Kosenko, A. M.; Salyaev, V. N. (Yarosl. Med. Inst., Yaroslavl, USSR). Farmakol. Toksikol. Nov. Prod. Khim. Sint., Mater. Resp. Konf., 3rd, Meeting Date 1974, 174-5. Edited by: Kuz'mitskii, B. B. Beloruss. Med. O-vo. Farmakol. Toksikol.: Minsk, USSR. (Russian) 1975. CODEN: 35ALA9. DOCUMENT TYPE: Conference CA Section: 4 (Toxicology) Gas-liq. chromatog. showed that EtBr [74-96-4], PrBr [106-94-5], BuBr [109-65-9], iso-BuBr [78-77-3], and isoamyl bromide [107-82-4] administered orally to rats at LD50 were deposited mainy in the brain, liver, and perirenal cellular system and excreted primarily by the lungs.
- Study of the haloalkylation of poly(4-vinylpyridine)
- Study of the haloalkylation of poly(4-vinylpyridine). Korshak, V. V.; Zubakova, L. B.; Zhovnirovskaya, A. B.; Kuz'menko, N. E. (Mosk. Khim.-Tekhnol. Inst. im. Mendeleeva, Moscow, USSR). Vysokomol. Soedin., Ser. B, 19(6), 428-30 (Russian) 1977. CODEN: VYSBAI. DOCUMENT TYPE: Journal CA Section: 35 (Synthetic High Polymers) Poly(4-vinylpyridine) (I) [25232-41-1] was prepd. by continuous polymn. in aq. H2SO4 and neutralization of the resulting salt with NaOH. Alkylation of I with EtBr [74-96-4], EtI [75-03-6], oe PrBr [106-94-5] gave the corresponding quaternary polymers of degree of substitution 28-48% in 35-68% yields. The degrees of substitution and the yields of quaternary polymers decreased on passing from EtBr to PrBr and from EtI to EtBr. The optimum conditions for prepn. of I and for its alkylation were given.
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