he company has advanced technology, as well as a large number of excellent R & D team, to provide customers from the grams to one hundred kilograms and tons of high-quality products, competitive prices and quality se T rvice Appearance:White or
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inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
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FOB Price: $139.0 / 210.0
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Min.Order:10 Kilogram
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inquiryN-NONADECANE CAS:629-92-5 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic intermediates,
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inquiryN-NONADECANE Chemical Properties Melting point 32 °C Boiling point 330 °C(lit.) density 0.786 g/mL at 25 °C(lit.) vapor density 9.27 (vs air) vapor pressure 1 mm Hg ( 133.2 °C) refractive index 1.4410 Fp 33
factory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
Hangzhou Huarong Pharm Co., Ltd.established since 2006 , has been actively developing specialty products for Finished Dosages, APIs, Intermediates, and Fine chemicals markets in North America, Europe, Korea, Japan, Mid-East and all over the World. Hu
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Type:Lab/Research institutions
inquiryShandong Mopai Biotechnology Co., LTD is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemicals. W
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Conditions | Yield |
---|---|
With hydrogen at 200℃; under 7500.75 Torr; for 24h; Microwave irradiation; | A 93% B n/a |
Conditions | Yield |
---|---|
With phosphorus pentachloride und erhitzen des Reaktionsprodukts mit Jodwasserstoffsaeure und Phosphor auf 240grad; | |
With hydrogenchloride; amalgamated zinc |
Conditions | Yield |
---|---|
With barium dihydroxide under 15 Torr; Destillation; |
cis-Octadecenoic acid
oenanthic acid
A
dodecane
B
icosane
C
n-nonadecane
D
(Z)-tricos-9-ene
Conditions | Yield |
---|---|
With sodium In methanol; n-heptane at 30 - 35℃; for 5h; electrolysis; Further byproducts given. Title compound not separated from byproducts; | A 21.6 % Chromat. B 0.4 % Chromat. C 3.7 % Chromat. D 39.5 % Chromat. |
2-Methyl-nonadecanenitrile
n-nonadecane
Conditions | Yield |
---|---|
With potassium; toluene; perhydrodibenzo-18-crown-6 Ambient temperature; Yield given; |
nonadeca-1,cis-3,cis-6,cis-9-tetraene
n-nonadecane
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal |
Conditions | Yield |
---|---|
under 15 Torr; |
Conditions | Yield |
---|---|
With air Oxidation; Formation of xenobiotics; Further byproducts given. Title compound not separated from byproducts; |
A
icosane
B
hepatdecane
C
n-nonadecane
D
adipic acid monomethyl ester
Conditions | Yield |
---|---|
With air at 1130℃; under 18001.4 Torr; Formation of xenobiotics; high pressure combustion; Further byproducts given. Title compound not separated from byproducts; |
n-nonadecane
Conditions | Yield |
---|---|
at 500℃; for 0.0277778h; Formation of xenobiotics; |
decalin
E
naphthalene
F
tetralin
G
octane
H
nonane
I
decane
J
dodecane
K
pentadecane
L
icosane
M
n-docosane
N
n-hexacosane
O
methane
P
n-heptane
Q
Tridecane
R
isotridecane
S
tetradecane
T
3-methyl-tridecane
U
2-methyltridecane
V
3-methyltetradecane
W
isopentadecane
X
3-methylpentadecane
Y
Hexadecane
Z
hepatdecane
[
3-methylhexadecane
\
2-Methyl hexadecane
]
octadecane
^
n-nonadecane
_
2-methyl-eicosane
`
n-tricosane
a
tetracosane
b
n-pentacosane
c
norpristane
Conditions | Yield |
---|---|
With Dimethyldisulphide; hydrogen; cobalt-molybdenum on alumina at 363℃; under 23252.3 Torr; for 120h; Product distribution / selectivity; |
(3Z,6Z)-3,6-Hexadecadienyl(triphenyl)phosphonium iodide
n-nonadecane
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) Na-Silazid 2: H2 / Pd/C View Scheme |
tetradeca-1,4-diyne
n-nonadecane
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: 1.) EtMgBr 2: 1.)CBr4/TPP; 2.)NaI 3: 52 percent 4: 1.) Na-Silazid 5: H2 / Pd/C View Scheme |
(3Z,6Z)-3,6-Hexadecadienyliodid
n-nonadecane
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 52 percent 2: 1.) Na-Silazid 3: H2 / Pd/C View Scheme |
3,6-Hexadecadiin-1-ol
n-nonadecane
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 1.)CBr4/TPP; 2.)NaI 2: 52 percent 3: 1.) Na-Silazid 4: H2 / Pd/C View Scheme |
benzopyrene
A
phthalic anhydride
B
pentadecane
C
2-(1-methylethyl)-1-pentene
D
Hexadecane
F
octadecane
G
n-nonadecane
H
heneicosane
R
butanoic vinyl anhydride
U
propyl benzoate
V
Di(2-ethylhexyl)phthalate
W
benzoic acid ethyl ester
X
2-isobutyl-3-methyl-pent-1-ene
Y
diisonoyl phthalate
Z
3-methylchrysene
Conditions | Yield |
---|---|
With oxygen; ozone In water |
Conditions | Yield |
---|---|
With hydrogen; Ni 55/5 P catalyst at 325℃; under 26618.1 - 104192 Torr; for 5h; Product distribution / selectivity; |
Conditions | Yield |
---|---|
With hydrogen; nickel/molybdenum on alumina at 325℃; under 78334.3 - 104192 Torr; Product distribution / selectivity; |
decane
A
pentadecane
B
icosane
C
n-docosane
D
Tridecane
E
tetradecane
F
Hexadecane
G
hepatdecane
H
octadecane
I
n-nonadecane
J
heneicosane
Conditions | Yield |
---|---|
With C22H41IrN2O2P2; Re2O7/Al2O3; 1,3,5-trimethyl-benzene at 175℃; for 168h; Inert atmosphere; |
Conditions | Yield |
---|---|
With 1% Pd/C Selcat Q6 In dodecane at 300℃; under 12751.3 Torr; for 2.5h; Inert atmosphere; | |
With photodecarboxylase from Chlorella variabilis NC64A In dimethyl sulfoxide at 37℃; for 14h; pH=8.5; Catalytic behavior; Irradiation; Sealed tube; Enzymatic reaction; |
Conditions | Yield |
---|---|
With hydrogen at 400℃; under 750.075 Torr; |
Conditions | Yield |
---|---|
With bis(1,5-cyclooctadiene)rhodium chloride; tris-(o-tolyl)phosphine at 177℃; for 16h; Schlenk technique; Inert atmosphere; | 82 %Spectr. |
Conditions | Yield |
---|---|
With hydrogen In n-heptane at 199.84℃; under 22502.3 Torr; Kinetics; Autoclave; |
BPA
A
n-nonadecane
B
4-isopropenylphenol
C
3-hydroxy-3-phenylpropanoic acid
Conditions | Yield |
---|---|
With Chaetomium strumarium G5I In acetonitrile at 35℃; for 6h; Reagent/catalyst; Time; |
BPA
A
Hexadecane
B
n-nonadecane
C
4-isopropenylphenol
D
3-hydroxy-3-phenylpropanoic acid
Conditions | Yield |
---|---|
With Thielavia arenaria HJ22 In acetonitrile at 35℃; for 12h; |
Conditions | Yield |
---|---|
In various solvent(s) |
n-nonadecane
(Z)-9-nonadecene
Conditions | Yield |
---|---|
With glutamic acid sodium salt; resting cells of a mutant; Rhodococcus sp. strain KSM-MT66 In phosphate buffer pH=7.0; Product distribution; Dehydrogenation; Microbiological reaction; |
hepatdecane
octadecane
n-nonadecane
A
2-methylheptane
B
3-methylheptane
C
Isobutane
D
methylbutane
E
2-Methylpentane
F
n-heptane
G
3-methyloctane
H
o-xylene
I
para-xylene
J
1,2,4-Trimethylbenzene
Conditions | Yield |
---|---|
With hydrogen; zeolite USY at 300℃; under 78334.3 - 104192 Torr; for 5h; Product distribution / selectivity; |
hepatdecane
octadecane
n-nonadecane
A
2-methylheptane
B
isodecane
C
ethanol
D
3-methylheptane
E
Isobutane
F
methylbutane
G
2-Methylpentane
H
n-heptane
I
3-methyloctane
J
Hexadecane
K
4-methylhexadecane
L
4-methylheptadecane
M
2-methylheptadecane
N
4-ethyltetradecane
Conditions | Yield |
---|---|
With hydrogen; Ni 55/5 P catalyst; mordenite zeolite at 300℃; under 78334.3 - 104192 Torr; for 5h; Product distribution / selectivity; | |
With hydrogen; zeolite Beta at 300℃; under 78334.3 - 104192 Torr; for 5h; Product distribution / selectivity; |
hepatdecane
octadecane
n-nonadecane
A
ethanol
B
Isobutane
C
methylbutane
D
2-Methylpentane
E
n-heptane
F
Tridecane
G
para-xylene
Conditions | Yield |
---|---|
With hydrogen; Ni 55/5 P catalyst; zeolite LZ-Y-84 at 300℃; under 78334.3 - 104192 Torr; for 5h; Product distribution / selectivity; |
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