Details
Manufacturer supply high quality DIMETHYL BRASSYLATE 1472-87-3 with ISO standards
- Molecular Formula: C15H28O4
- Molecular Weight: 272.385
- Appearance/Colour: Powder
- Vapor Pressure: 0.000208mmHg at 25°C
- Melting Point: 35-37 °C(lit.)
- Refractive Index: 1.443
- Boiling Point: 326.999 °C at 760 mmHg
- Flash Point: 140.751 °C
- PSA: 52.60000
- Density: 0.962 g/cm3
- LogP: 3.62350
DIMETHYL BRASSYLATE(Cas 1472-87-3) Usage
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General Description |
DIMETHYL BRASSYLATE is a synthetic fragrance ingredient commonly used in perfumes, personal care products, and household goods. It is classified as an ester and is created through the chemical reaction of brassic acid and methanol. DIMETHYL BRASSYLATE is known for its warm, sweet, and slightly floral scent, resembling that of a natural musk. It is often used to enhance the longevity and sillage of fragrances, as well as to impart a subtle, lingering aroma. However, |
InChI:InChI=1/C15H28O4/c1-18-14(16)12-10-8-6-4-3-5-7-9-11-13-15(17)19-2/h3-13H2,1-2H3
1472-87-3 Relevant articles
Chemical synthesis of diglucosyl diacylglycerols utilizing glycosyl donors with stereodirecting cyclic silyl protective groups
Takato, Koichi,Kurita, Motoki,Yagami, Nahoko,Tanaka, Hide-Nori,Ando, Hiromune,Imamura, Akihiro,Ishida, Hideharu
, (2019/08/01)
Chemical syntheses of the bacterial digl...
Six New Polyacetylenic Alcohols from the Marine Sponges Petrosia sp. and Halichondria sp.
Gabriel, Adeyemi Francis,Li, Zhen,Kusuda, Ryouhei,Tanaka, Chiaki,Miyamoto, Tomofumi
, p. 469 - 475 (2015/09/07)
Six new polyacetylenic alcohols, termed ...
Metal/bromide autoxidation of triglycerides for the preparation of FAMES to improve the cold-flow characteristics of biodiesel
Phung, Peter,Rowlands, William N.,Thiyakesan, Appadurai,Benndorf, Paul,Masters, Anthony F.,Maschmeyer, Thomas
, p. 162 - 168 (2014/07/07)
Triglyceride autoxidation using a homoge...
Biosynthesis of defensive coccinellidae alkaloids: Incorporation of fatty acids in adaline, coccinelline, and harmonine
Haulotte, Eveline,Laurent, Pascal,Braekman, Jean-Claude
experimental part, p. 1907 - 1912 (2012/05/31)
In this study, we report on in vitro inc...
1472-87-3 Process route
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-
67-56-1
methanol
-
-
112-39-0
hexadecanoic acid methyl ester
-
-
627-93-0
hexanedioic acid dimethyl ester
-
-
1732-10-1
Dimethyl azelate
-
-
1731-84-6
nonanoic acid methyl ester
-
-
110-42-9
Methyl decanoate
-
-
1731-86-8
methyl undecanoate
-
-
111-82-0
methyl n-dodecanoate
-
-
1731-88-0
methyl tridecanoate
-
-
124-10-7
methyl myristoate
-
-
1732-08-7
dimethyl 1,7-heptanedioate
-
-
1732-09-8
dimethyl subarate
-
-
106-79-6
dimethyl sebacate
-
-
4567-98-0
dimethyl undecanedioate
-
-
1731-79-9
dodecanedioic acid dimethyl ester
-
-
1472-87-3
dimethyl 1,11-undecanedicarboxylate
-
-
5024-21-5
dimethyl tetradecanedioate
-
-
36575-82-3
dimethyl pentadecanedioate
| Conditions | Yield |
|---|---|
|
With
cobalt(II) acetate; manganese(II) acetate; zirconium(IV) chloride; acetic acid; potassium bromide;
at 150 ℃;
for 2h;
under 30003 Torr;
Autoclave;
|
-
-
67-56-1
methanol
-
-
505-52-2
brassylic acid
-
-
1472-87-3
dimethyl 1,11-undecanedicarboxylate
| Conditions | Yield |
|---|---|
|
With
sulfuric acid;
for 5h;
Heating;
|
98%
|
|
With
sulfuric acid;
for 2h;
Reflux;
|
91%
|
|
With
thionyl chloride;
|
65%
|
|
With
sulfuric acid;
Heating;
|
|
|
With
thionyl chloride;
at 20 ℃;
for 6h;
|
|
|
With
thionyl chloride;
at 0 ℃;
for 15h;
Inert atmosphere;
Reflux;
|
1472-87-3 Upstream products
-
67-56-1
methanol
-
111-81-9
Methyl 10-undecenoate
-
64-19-7
acetic acid
-
1186-73-8
methanetricarboxylic acid trimethyl ester
1472-87-3 Downstream products
-
13362-52-2
1,13-tridecanediol
-
116754-58-6
13-bromo-1-tridecylalcohol
-
15541-01-2
hexacosane-1,26-diol
-
14502-46-6
ω-tridecyn-1-oic acid
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