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489603

Sigma-Aldrich

Hexadecane-d34

98 atom % D

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5 G
₹2,838.00
25 G
₹6,864.00

₹2,838.00


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5 G
₹2,838.00
25 G
₹6,864.00

About This Item

Linear Formula:
CD3(CD2)14CD3
CAS Number:
Molecular Weight:
260.65
MDL number:
UNSPSC Code:
12352002
PubChem Substance ID:
NACRES:
NA.12

₹2,838.00


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isotopic purity

98 atom % D

Quality Level

form

liquid

refractive index

n20/D 1.434 (lit.)

bp

287 °C (lit.)

mp

18 °C (lit.)

density

0.887 g/mL at 25 °C

mass shift

M+34

SMILES string

[2H]C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])[2H]

InChI

1S/C16H34/c1-3-5-7-9-11-13-15-16-14-12-10-8-6-4-2/h3-16H2,1-2H3/i1D3,2D3,3D2,4D2,5D2,6D2,7D2,8D2,9D2,10D2,11D2,12D2,13D2,14D2,15D2,16D2

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This Item
485799493198613681
isotopic purity

98 atom % D

isotopic purity

99 atom % 13C

isotopic purity

98 atom % D

isotopic purity

≥98 atom % D

mass shift

M+34

mass shift

M+2

mass shift

M+32

mass shift

M+33

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

form

liquid

form

-

form

-

form

solid

mp

18 °C (lit.)

mp

18 °C (lit.)

mp

8-10 °C (lit.)

mp

54-56 °C (lit.)

refractive index

n20/D 1.434 (lit.)

refractive index

n20/D 1.434 (lit.)

refractive index

n20/D 1.432 (lit.)

refractive index

-

Packaging

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

Pictograms

Health hazard

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Asp. Tox. 1

Supplementary Hazards

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

275.0 °F - closed cup

Flash Point(C)

135 °C - closed cup


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Synthesis of novel halopyridinylboronic acids and esters. Part 2: 2, 4, or 5-Halopyridin-3-yl-boronic acids and esters.
Bouillon A, et al.
Tetrahedron, 58(17), 3323-3328 (2002)
Synthesis of the first thieno-d-carboline: Fluorescence studies in solution and in lipid vesicles.
Queiroz MJRP, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 181(2), 290-296 (2006)
Alexandre Bouillon et al.
The Journal of organic chemistry, 68(26), 10178-10180 (2003-12-20)
Regioselective and univocal Suzuki cross-coupling reactions performed on halopyridinyl boronic acids provide a flexible and versatile route to a multigram scale synthesis of 2,2'-dichloro-3,4'-bipyridine 14, which allows couplings with excess pyridin-3-yl boronic acid to give a new and efficient two-step
Use of hydrogen bonds to control molecular aggregation. behavior of dipyridones and pyridone-pyrimidones designed to form cyclic triplexes.
Boucher E, et al.
The Journal of Organic Chemistry, 60(5), 1408-1412 (1995)
Maria-João R P Queiroz et al.
Bioorganic & medicinal chemistry, 14(20), 6827-6831 (2006-07-18)
ortho-Chlorodiarylamines in the 2,3,7-trimethylbenzo[b]thiophene series were prepared in high yields (70-85%) by C-N palladium-catalyzed cross-coupling using P(t-Bu)(3) as ligand and NaOt-Bu as base. A palladium-assisted C-C intramolecular cyclization of the coupling products gave thienocarbazoles and the dechlorinated diarylamines. Studies of

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