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1-Hexadecylamine,CAS:143-27-1
Cas No: 143-27-1
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Hexadecylamine
Cas No: 143-27-1
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1-Hexadecylamine TOP1 supplier
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Factory price Cosmetic PALMITAMINE 143-27-1 Manufacturer
Cas No: 143-27-1
USD $ 0.1-0.1 / Gram 1 Gram 100 Metric Ton/Year Xi'an Xszo Chem Co., Ltd. Contact Supplier
Factory Supply Hexadecylamine
Cas No: 143-27-1
No Data 1 1 Ality Chemical Corporation Contact Supplier
1-hexadecanamine hydrofluoride
Cas No: 143-27-1
No Data 10 Milligram Amadis Chemical Co., Ltd. Contact Supplier
Palmitylamine
Cas No: 143-27-1
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143-27-1 1-Hexadecylamine
Cas No: 143-27-1
USD $ 1000.0-1000.0 / Kilogram 1 Kilogram 1 Metric Ton/Day Henan Tianfu Chemical Co., Ltd. Contact Supplier
1-HexadecylaminemasssupplyfactorysalesHighquality99%CASNO143-27-1ISO9001:2015REACHverifiedproducer
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USD $ 1.0-2.0 / Metric Ton 1 Metric Ton 2 Metric Ton/Day Hubei Jusheng Technology Co., Ltd., Contact Supplier
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143-27-1 Usage

General Description

A white waxy solid with an ammonia-like odor. Insoluble in water and less dense than water. Hence floats on water. Contact may irritate skin, eyes and mucous membranes. May be toxic by ingestion, inhalation or skin absorption. Used to make other chemicals.

Reactivity Profile

HEXADECANAMINE neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.

Health Hazard

TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Uses

Dental caries prophylactic.

Air & Water Reactions

Insoluble in water.

Purification Methods

Crystallise the base from thiophene-free *benzene and dry under vacuum over P2O5. Store away from CO2 [Beilstein 4 IV 818.]

Fire Hazard

Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Some are oxidizers and may ignite combustibles (wood, paper, oil, clothing, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated.

Chemical Properties

white low melting crystalline mass or chunks
InChI:InChI=1/C16H35N.C2H4O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17;1-2(3)4/h2-17H2,1H3;1H3,(H,3,4)

143-27-1 Well-known Company Product Price

Brand (Code)Product description CAS number Packaging Price Detail
Alfa Aesar (B22459)  1-Hexadecylamine, tech. 90%, remainder mainly 1-octadecylamine    143-27-1 25g 261.0CNY Detail
Alfa Aesar (B22459)  1-Hexadecylamine, tech. 90%, remainder mainly 1-octadecylamine    143-27-1 250g 363.0CNY Detail
Alfa Aesar (B22459)  1-Hexadecylamine, tech. 90%, remainder mainly 1-octadecylamine    143-27-1 1000g 1160.0CNY Detail

143-27-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Hexadecylamine

1.2 Other means of identification

Product number -
Other names palmitylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Lubricants and lubricant additives
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:143-27-1 SDS

143-27-1Synthetic route

N-Boc-hexadecylamine
876360-84-8

N-Boc-hexadecylamine

hexadecylamine
143-27-1

hexadecylamine

Conditions
ConditionsYield
With 3-butyl-l-methyl-1H-imidazol-3-iumtrifloroacetate In 1,4-dioxane; water at 80℃; for 1.5h;96%
cetyl azide
66143-67-7

cetyl azide

hexadecylamine
143-27-1

hexadecylamine

Conditions
ConditionsYield
With tellurium; water at 275℃; for 4h;91%
1-Hexadecanol
36653-82-4

1-Hexadecanol

hexadecylamine
143-27-1

hexadecylamine

Conditions
ConditionsYield
With aluminum oxide; ammonia at 380 - 400℃; under 88260.9 - 95616 Torr;
1-Chlorohexadecan
4860-03-1

1-Chlorohexadecan

A

hexadecylamine
143-27-1

hexadecylamine

B

dihexadecylamine
16724-63-3

dihexadecylamine

Conditions
ConditionsYield
With ethanol; ammonia at 170℃;
palmitonitrile
629-79-8

palmitonitrile

hexadecylamine
143-27-1

hexadecylamine

Conditions
ConditionsYield
With ethanol; hydrogen; sodium at 120℃; under 14710.2 Torr;
With sodium hydroxide; nickel at 70℃; Hydrogenation;
With kieselguhr; ammonia; nickel at 135℃; Hydrogenation;
N-hexadecyl-phthalimide
61020-43-7

N-hexadecyl-phthalimide

hexadecylamine
143-27-1

hexadecylamine

Conditions
ConditionsYield
With sodium hydroxide; ethanol
With ethanol; hydrazine hydrate anschliessendes Kochen mit konz. HCl;
hexadecanyl bromide
112-82-3

hexadecanyl bromide

hexadecylamine
143-27-1

hexadecylamine

Conditions
ConditionsYield
With ammonia at 50℃;
Palmitamide
629-54-9

Palmitamide

hexadecylamine
143-27-1

hexadecylamine

Conditions
ConditionsYield
With lithium aluminium tetrahydride; diethyl ether
With lithium aluminium tetrahydride In tetrahydrofuran for 1h;
1-iodohexadecane
544-77-4

1-iodohexadecane

hexadecylamine
143-27-1

hexadecylamine

Conditions
ConditionsYield
With ammonia In ethanol; benzene
Yield given. Multistep reaction;
Multi-step reaction with 2 steps
2: ethanol; NaOH
View Scheme
palmitohydroxamic acid
17698-04-3

palmitohydroxamic acid

hexadecylamine
143-27-1

hexadecylamine

Conditions
ConditionsYield
With lithium aluminium tetrahydride In tetrahydrofuran Heating;
Naphthalene-1,8-dicarboxylic acid 1-hexadecylamide 8-phenylamide
104944-87-8

Naphthalene-1,8-dicarboxylic acid 1-hexadecylamide 8-phenylamide

A

hexadecylamine
143-27-1

hexadecylamine

B

2-phenylbenzo[de]isoquinoline-1,3-dione
6914-98-3

2-phenylbenzo[de]isoquinoline-1,3-dione

C

2-Hexadecyl-benzo[de]isoquinoline-1,3-dione
74240-30-5

2-Hexadecyl-benzo[de]isoquinoline-1,3-dione

D

aniline
62-53-3

aniline

Conditions
ConditionsYield
at 270℃; for 0.333333h;
C16H35N(1+)*C12H4N4(1-)

C16H35N(1+)*C12H4N4(1-)

A

hexadecylamine
143-27-1

hexadecylamine

B

7,7',8,8'-tetracyanoquinodimethane
1518-16-7

7,7',8,8'-tetracyanoquinodimethane

Conditions
ConditionsYield
In dichloromethane at 25℃; Rate constant;
ethanol
64-17-5

ethanol

palmitonitrile
629-79-8

palmitonitrile

sodium

sodium

hexadecylamine
143-27-1

hexadecylamine

ethanol
64-17-5

ethanol

1-Chlorohexadecan
4860-03-1

1-Chlorohexadecan

ammonia
7664-41-7

ammonia

A

hexadecylamine
143-27-1

hexadecylamine

B

dihexadecylamine
16724-63-3

dihexadecylamine

Conditions
ConditionsYield
at 170℃;
1-aminooctadecane
124-30-1

1-aminooctadecane

hexadecylamine
143-27-1

hexadecylamine

Conditions
ConditionsYield
With cetyltrimethylammonim bromide at 269.84℃; Inert atmosphere;
n-hexadecanoyl chloride
112-67-4

n-hexadecanoyl chloride

hexadecylamine
143-27-1

hexadecylamine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: ammonia / dichloromethane
2: lithium aluminium tetrahydride / tetrahydrofuran / 1 h
View Scheme
1-hexadecylcarboxylic acid
57-10-3

1-hexadecylcarboxylic acid

hexadecylamine
143-27-1

hexadecylamine

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: oxalyl dichloride / benzene / 3 h
2: ammonia / dichloromethane
3: lithium aluminium tetrahydride / tetrahydrofuran / 1 h
View Scheme
With D-glucose; pyridoxal 5'-phosphate; glucose dehydrogenase (CDX-901) from Codexis; NADP; isopropylamine; magnesium chloride In n-heptane; dimethyl sulfoxide at 30℃; for 20h; pH=8; Green chemistry; Enzymatic reaction;
glyceroltripalmitate
555-44-2

glyceroltripalmitate

A

hexadecylamine
143-27-1

hexadecylamine

B

dihexadecylamine
16724-63-3

dihexadecylamine

Conditions
ConditionsYield
With ammonium hydroxide; hydrogen at 220℃; under 41254.1 Torr; for 36h; Autoclave;A 54 %Chromat.
B 19 %Chromat.
hexadecylamine
143-27-1

hexadecylamine

bromocyane
506-68-3

bromocyane

hexadecyl cyanamide
97226-87-4

hexadecyl cyanamide

Conditions
ConditionsYield
100%
N,N-dimethylacetamide dimethyl acetal
18871-66-4

N,N-dimethylacetamide dimethyl acetal

hexadecylamine
143-27-1

hexadecylamine

N'-hexadecyl-N,N-dimethylacetamidine

N'-hexadecyl-N,N-dimethylacetamidine

Conditions
ConditionsYield
at 60℃; for 0.166667 - 0.333333h; Product distribution / selectivity;100%
hexadecylamine
143-27-1

hexadecylamine

4-hydroxy-benzaldehyde
123-08-0

4-hydroxy-benzaldehyde

C23H39NO
1246401-83-1

C23H39NO

Conditions
ConditionsYield
at 20℃; for 12h;100%
In toluene
With acetic acid In ethanol for 3h; Reflux;
hexadecylamine
143-27-1

hexadecylamine

meta-hydroxybenzaldehyde
100-83-4

meta-hydroxybenzaldehyde

C23H39NO
1246401-87-5

C23H39NO

Conditions
ConditionsYield
at 20℃; for 12h;100%
hexadecylamine
143-27-1

hexadecylamine

2-Bromoacetyl bromide
598-21-0

2-Bromoacetyl bromide

2-bromo-N-hexadecylethanamide
1138445-61-0

2-bromo-N-hexadecylethanamide

Conditions
ConditionsYield
With potassium carbonate In dichloromethane; water at 5 - 20℃; for 4h;100%
With potassium carbonate In dichloromethane; water at 0 - 20℃; for 16h;99%
hexadecylamine
143-27-1

hexadecylamine

(S)-methyl 3-(tert-butoxy)-2-((R)-2-((tert-butoxycarbonyl)amino)-3-((2-hydroxyethyl)thio)propanamido)propanoate
1346422-43-2

(S)-methyl 3-(tert-butoxy)-2-((R)-2-((tert-butoxycarbonyl)amino)-3-((2-hydroxyethyl)thio)propanamido)propanoate

(2S,5R)-methyl 5-amino-2-(hydroxymethyl)-4,11-dioxo-10-oxa-7-thia-3,12-diazaoctacosan-1-oate

(2S,5R)-methyl 5-amino-2-(hydroxymethyl)-4,11-dioxo-10-oxa-7-thia-3,12-diazaoctacosan-1-oate

Conditions
ConditionsYield
Stage #1: (S)-methyl 3-(tert-butoxy)-2-((R)-2-((tert-butoxycarbonyl)amino)-3-((2-hydroxyethyl)thio)propanamido)propanoate With trifluoroacetic acid
Stage #2: hexadecylamine
100%
hexadecylamine
143-27-1

hexadecylamine

(7-(carboxymethyl)-1,3,6,8-tetraoxo-3,6,7,8-tetrahydro-1H-benzo[lmn][3,8]phenanthrolin-2-yl)-acetic acid
5880-06-8

(7-(carboxymethyl)-1,3,6,8-tetraoxo-3,6,7,8-tetrahydro-1H-benzo[lmn][3,8]phenanthrolin-2-yl)-acetic acid

C18H10N2O8*2C16H35N

C18H10N2O8*2C16H35N

Conditions
ConditionsYield
In methanol at 20℃;100%
hexadecylamine
143-27-1

hexadecylamine

(R)-1-(tert-butoxycarbonyl)pyrrolidine-3-carboxylic acid
72925-16-7

(R)-1-(tert-butoxycarbonyl)pyrrolidine-3-carboxylic acid

tert-butyl (R)-3-(hexadecylcarbamoyl)pyrrolidine-1-carboxylate

tert-butyl (R)-3-(hexadecylcarbamoyl)pyrrolidine-1-carboxylate

Conditions
ConditionsYield
With 2,6-dimethylpyridine; 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 3.5h;100%
With 2,6-dimethylpyridine; 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 3.5h;100%
hexadecylamine
143-27-1

hexadecylamine

palladium palmitate

palladium palmitate

bis(hexadecylamine)palladium(II) palmitate

bis(hexadecylamine)palladium(II) palmitate

Conditions
ConditionsYield
In dichloromethane at 40℃; for 2h;100%
hexadecylamine
143-27-1

hexadecylamine

palladium diacetate
3375-31-3

palladium diacetate

bis(hexadecylamine)palladium(II) acetate

bis(hexadecylamine)palladium(II) acetate

Conditions
ConditionsYield
In dichloromethane at 40℃; for 2h;100%
hexadecylamine
143-27-1

hexadecylamine

acrylonitrile
107-13-1

acrylonitrile

N-hexadecyl-bis(2-cyanoethyl)amine
1555-63-1

N-hexadecyl-bis(2-cyanoethyl)amine

Conditions
ConditionsYield
In methanol at 45℃; for 16h;99%
N,N-dimethylacetamide dimethyl acetal
18871-66-4

N,N-dimethylacetamide dimethyl acetal

hexadecylamine
143-27-1

hexadecylamine

N'-hexadecyl-N,N-dimethylacetimidamide

N'-hexadecyl-N,N-dimethylacetimidamide

Conditions
ConditionsYield
With dimethyl amine In tetrahydrofuran at 20℃; for 18.25h; Darkness; chemoselective reaction;99%
With dimethyl amine In tetrahydrofuran for 18h; Darkness;99%
at 70℃; for 1h;
hexadecylamine
143-27-1

hexadecylamine

1-cyano-cyclopropanecarboxylic acid
6914-79-0

1-cyano-cyclopropanecarboxylic acid

1-cyano-N-hexadecylcyclopropanecarboxamide
1266666-37-8

1-cyano-N-hexadecylcyclopropanecarboxamide

Conditions
ConditionsYield
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 4h; Inert atmosphere;99%
hexadecylamine
143-27-1

hexadecylamine

ethyl 1,5-diphenyl-1H-pyrazole-3-carboxylate
17355-75-8

ethyl 1,5-diphenyl-1H-pyrazole-3-carboxylate

C32H45N3O
1428261-49-7

C32H45N3O

Conditions
ConditionsYield
Stage #1: hexadecylamine With trimethylaluminum In n-heptane; dichloromethane at 20℃; for 1h; Inert atmosphere;
Stage #2: ethyl 1,5-diphenyl-1H-pyrazole-3-carboxylate In n-heptane; dichloromethane Reflux;
Stage #3: With hydrogenchloride In n-heptane; dichloromethane; water at 40℃; for 0.5h;
99%
2-methyl-4-oxo-3,1-benzoxazine
525-76-8

2-methyl-4-oxo-3,1-benzoxazine

hexadecylamine
143-27-1

hexadecylamine

3-hexadecyl-2-methylquinazolin-4(3H)-one

3-hexadecyl-2-methylquinazolin-4(3H)-one

Conditions
ConditionsYield
Stage #1: 2-methyl-4-oxo-3,1-benzoxazine In ethanol at 20℃; for 0.0833333h;
Stage #2: hexadecylamine In ethanol at 100℃; for 6h;
98.1%
hexadecylamine
143-27-1

hexadecylamine

stearic acid
57-11-4

stearic acid

N-hexadecyl srearamide
81126-74-1

N-hexadecyl srearamide

Conditions
ConditionsYield
With nano sulfated-TiO2 at 115℃; under 760.051 Torr; for 2.5h; Neat (no solvent);98%
hexadecylamine
143-27-1

hexadecylamine

18α-glycyrrhizic acid

18α-glycyrrhizic acid

C42H62O16*C16H35N

C42H62O16*C16H35N

Conditions
ConditionsYield
In methanol Reflux;98%
hexadecylamine
143-27-1

hexadecylamine

propionic acid
802294-64-0

propionic acid

N-hexadecylpropanamide
59453-61-1

N-hexadecylpropanamide

Conditions
ConditionsYield
With magnesium In toluene at 160℃; for 2h;98%
Stage #1: hexadecylamine; propionic acid In methanol; water at 20℃;
Stage #2: With N-tosylimidazole In N,N-dimethyl-formamide at 100℃; for 1h;
Stage #3: With triethylamine In N,N-dimethyl-formamide at 100℃; for 6h;
hexadecylamine
143-27-1

hexadecylamine

acrylic acid methyl ester
292638-85-8

acrylic acid methyl ester

N-hexadecyl-β-aminopropionic acid methyl ester

N-hexadecyl-β-aminopropionic acid methyl ester

Conditions
ConditionsYield
at 60℃; for 6.5h; Michael Addition;98%
In methanol at 35℃; for 8h; Reflux;
hexadecylamine
143-27-1

hexadecylamine

C11H14O6

C11H14O6

(3aS,4R,7S,8S,8aR)-N-hexadecyl-2,2-dimethyl-6-oxohexahydro-4,7-methano[1,3]-dioxolo[4–c]oxepin-8-carboxamide

(3aS,4R,7S,8S,8aR)-N-hexadecyl-2,2-dimethyl-6-oxohexahydro-4,7-methano[1,3]-dioxolo[4–c]oxepin-8-carboxamide

Conditions
ConditionsYield
Stage #1: C11H14O6 With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 0.25h; Inert atmosphere;
Stage #2: hexadecylamine In dichloromethane; N,N-dimethyl-formamide at 20℃; for 2h; Inert atmosphere;
98%
succinic acid anhydride
108-30-5

succinic acid anhydride

hexadecylamine
143-27-1

hexadecylamine

4-(hexadecylamino)-4-oxobutanoic acid
3384-46-1

4-(hexadecylamino)-4-oxobutanoic acid

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃; for 3h; Inert atmosphere;98%
In tetrahydrofuran at 40℃;
hexadecylamine
143-27-1

hexadecylamine

3,4-dimethoxy-3-cyclobutene-1,2-dione
5222-73-1

3,4-dimethoxy-3-cyclobutene-1,2-dione

C36H68N2O2
1428906-20-0

C36H68N2O2

Conditions
ConditionsYield
In methanol at 20℃; Inert atmosphere;97.5%
hexadecylamine
143-27-1

hexadecylamine

dihexadecylamine
16724-63-3

dihexadecylamine

Conditions
ConditionsYield
With Co2Rh2/C In toluene at 180℃; under 760.051 Torr; for 18h; Autoclave; Inert atmosphere;97%
In aluminum nickel; water; benzene73%
With nickel at 200℃;
hexadecylamine
143-27-1

hexadecylamine

2,4-bis(3,5-di-tert-butyl-4-hydroxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide
58851-58-4

2,4-bis(3,5-di-tert-butyl-4-hydroxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide

Diacetone D-glucose
2595-05-3

Diacetone D-glucose

C26H41O7PS2*C16H35N

C26H41O7PS2*C16H35N

Conditions
ConditionsYield
Stage #1: 2,4-bis(3,5-di-tert-butyl-4-hydroxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide; Diacetone D-glucose In benzene at 20℃; for 1h; Inert atmosphere;
Stage #2: hexadecylamine In benzene at 20℃; for 1h; Inert atmosphere;
97%
hexadecylamine
143-27-1

hexadecylamine

benzaldehyde
100-52-7

benzaldehyde

N-(phenylmethylene)-1-hexadecanamine
47377-65-1

N-(phenylmethylene)-1-hexadecanamine

Conditions
ConditionsYield
With 3 A molecular sieve In dichloromethane at 40℃; for 6h; Condensation;96%
In toluene for 2h; Heating;
3,6-bis-(3,5-dimethyl-pyrazol-1-yl)-1,2,4,5-tetrazine
30169-25-6

3,6-bis-(3,5-dimethyl-pyrazol-1-yl)-1,2,4,5-tetrazine

hexadecylamine
143-27-1

hexadecylamine

A

3,5-dimethyl-1H-pyrazole
67-51-6

3,5-dimethyl-1H-pyrazole

B

[6-(3,5-dimethyl-pyrazol-1-yl)-[1,2,4,5]tetrazin-3-yl]-hexadecyl-amine

[6-(3,5-dimethyl-pyrazol-1-yl)-[1,2,4,5]tetrazin-3-yl]-hexadecyl-amine

Conditions
ConditionsYield
In acetonitrile at 20 - 25℃; Substitution;A n/a
B 96%
potassium hexafluorophosphate
17084-13-8

potassium hexafluorophosphate

hexadecylamine
143-27-1

hexadecylamine

(η6-chlorobenzene)(η5-pentamethylcyclopentadienyl)iron hexafluorophosphate

(η6-chlorobenzene)(η5-pentamethylcyclopentadienyl)iron hexafluorophosphate

(η6-hexadecylaminobenzene)(η5-pentamethylcyclopentadienyl)iron hexafluorophosphate

(η6-hexadecylaminobenzene)(η5-pentamethylcyclopentadienyl)iron hexafluorophosphate

Conditions
ConditionsYield
In dichloromethane; water the Fe-complex was stirred with the amine in CH2Cl2 under Ar at room temp. for 24 h, then a satd. aq. soln. of KPF4 was added;; the org. layer was separated, dried with MgSO4, concd. and pptd. by mixing with hexane; the crude prod. was recrystd. from MeOH/hexane 1:1; IR and (1)H-NMR spectroscopy;;96%
hexadecylamine
143-27-1

hexadecylamine

2-Nitrobenzenesulfonyl chloride
1694-92-4

2-Nitrobenzenesulfonyl chloride

2-nitro-N-hexadecylbenzenesulfonamide
198971-44-7

2-nitro-N-hexadecylbenzenesulfonamide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 23℃; for 1.25h; Large scale reaction;96%
tetradec-1-en-1-ylsuccinic anhydride
76386-10-2

tetradec-1-en-1-ylsuccinic anhydride

hexadecylamine
143-27-1

hexadecylamine

C34H65NO3

C34H65NO3

Conditions
ConditionsYield
With pyridine at 80℃; for 3h;96%

143-27-1Related news

1-Hexadecylamine (cas 143-27-1) as both reducing agent and stabilizer to synthesize Au and Ag nanoparticles and their SERS application09/29/2019

1-Hexadecylamine (HDA)-capped Au and Ag nanoparticles (NPs) have been successfully prepared by a one-pot solution growth method. The HDA is used as both reducing agent and stabilizer in the synthetic process is favorable for investigating the capping mechanism of Au and Ag NPs’ surface. The gro...detailed

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