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112-71-0

1-Bromotetradecane

CAS: 112-71-0

Molecular Formula: C14H29Br

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112-71-0 - Names and Identifiers

Name 1-Bromotetradecane
Synonyms 1-Bromtetradecan
Myristyl bromide
MYRISTYL BROMIDE
Bromotetradecane
BROMOTETRADECANE
Tetradecyl bromide
1-BROMOTETRADECANE
1-Bromotetradecane
TETRADECYL BROMIDE
1-tetradecylbromide
N-Tetradecyl Bromide
N-TETRADECYL BROMIDE
1-Tetradecyl bromide
CAS 112-71-0
EINECS 203-999-3
InChI InChI=1/C14H29Br/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h2-14H2,1H3

112-71-0 - Physico-chemical Properties

Molecular FormulaC14H29Br
Molar Mass277.28
Density0.932g/mLat 25°C(lit.)
Melting Point5-6°C(lit.)
Boling Point175-178°C20mm Hg(lit.)
Flash Point>230°F
Water Solubilityinsoluble
Solubility Chloroform
Vapor Presure0.00131mmHg at 25°C
AppearanceLiquid
ColorClear yellow
BRN1742640
Storage ConditionStore below +30°C.
StabilityStable. Incompatible with strong bases, strong oxidizing agents.
Refractive Indexn20/D 1.460(lit.)
Physical and Chemical Properties

density 0.93
melting point 5-6°C
boiling point 175-178°C (20 mmHg)
refractive index 1.459-1.461
flash point 149°C
water-soluble insoluble

UseFor Organic synthesis

112-71-0 - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk CodesR36/37/38 - Irritating to eyes, respiratory system and skin.
R22 - Harmful if swallowed
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 - Wear suitable protective clothing.
S24/25 - Avoid contact with skin and eyes.
WGK Germany3
TSCAYes
HS Code29033036

112-71-0 - 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)
Use organic synthesis intermediates.
for organic synthesis, can be used for the synthesis of medicine and other fine chemicals.
production method is obtained from the bromination of decanol. After the addition of decadiol was added to the reaction Pan, sulfuric acid was added dropwise with stirring, and stirring was continued for half an hour after the addition. Hydrobromic acid was then added and heated to 99-101 °c for 8H. After cooling to 30 ° C., the stirring was stopped and left for 12h, the upper oil was separated and adjusted to pH 8 with 10% sodium carbonate solution. The aqueous layer was separated, and the oil was washed twice with an equal volume of 50% ethanol. The washed oil was added with sodium carbonate, stirred intermittently, and dried for 24 hours. Filtered to obtain the finished product.
Last Update:2024-04-10 22:29:15
112-71-0
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