| Identification | More | [Name]
Decanal | [CAS]
112-31-2 | [Synonyms]
1-DECANAL
ALDEHYDE C-10
CAPRALDEHYDE
CAPRIC ALDEHYDE
CAPRINALDEHYDE
DECANAL
DECANALDEHYDE
DECYL ALDEHYDE
FEMA 2362
N-C10 ALDEHYDE
N-CAPRINALDEHYDE
N-DECANAL
N-DECYL ALDEHYDE
1-Decyl aldehyde
1-decylaldehyde
1-nonanecarbaldehyde
C-10 Aldehyde
c-10aldehyde
Caprinaldehyd
Caprinic aldehyde | [EINECS(EC#)]
203-957-4 | [Molecular Formula]
C10H20O | [MDL Number]
MFCD00007031 | [Molecular Weight]
156.27 | [MOL File]
112-31-2.mol |
| Chemical Properties | Back Directory | [Appearance]
colourless liquid, an important component of citrus | [Melting point ]
7 °C
| [Boiling point ]
207-209 °C (lit.) | [density ]
0.83 g/mL at 25 °C(lit.)
| [vapor density ]
>1 (vs air)
| [vapor pressure ]
~0.15 mm Hg ( 20 °C)
| [FEMA ]
2362 | [refractive index ]
n20/D 1.428(lit.)
| [Fp ]
186 °F
| [storage temp. ]
2-8°C
| [solubility ]
Acetonitrile (Slightly), Chloroform (Sparingly), Methanol (Slightly) | [form ]
liquid
| [color ]
clear, colorless
| [Odor]
pleasant smell | [Stability:]
Stable. Flammable. Incompatible with strong oxidizing agents. | [biological source]
synthetic | [Odor Threshold]
0.0004ppm | [Odor Type]
aldehydic | [Water Solubility ]
INSOLUBLE | [Thermal Conductivity]
0.144 W/(m·K) at 25 ℃ | [Sensitive ]
Air Sensitive | [JECFA Number]
104 | [BRN ]
1362530 | [Henry's Law Constant]
6.3×10-3 mol/(m3Pa) at 25℃, Brockbank (2013) | [Dielectric constant]
8.1（Ambient） | [Major Application]
cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care | [Cosmetics Ingredients Functions]
FRAGRANCE | [InChI]
1S/C10H20O/c1-2-3-4-5-6-7-8-9-10-11/h10H,2-9H2,1H3 | [InChIKey]
KSMVZQYAVGTKIV-UHFFFAOYSA-N | [SMILES]
[H]C(=O)CCCCCCCCC | [LogP]
3.8 at 35℃ | [CAS DataBase Reference]
112-31-2(CAS DataBase Reference) | [NIST Chemistry Reference]
Decanal(112-31-2) | [EPA Substance Registry System]
112-31-2(EPA Substance) |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H319 | [Precautionary statements ]
P264-P280-P305+P351+P338-P337+P313 | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [RIDADR ]
3082 | [WGK Germany ]
2
| [RTECS ]
HD6000000
| [F ]
8-10-23 | [Autoignition Temperature]
200 °C | [Hazard Note ]
Irritant | [TSCA ]
Yes | [REACH Registrations]
Active | [HazardClass ]
9 | [PackingGroup ]
III | [HS Code ]
29121900 | [Storage Class]
10 - Combustible liquids | [Hazard Classifications]
Aquatic Chronic 3
Eye Irrit. 2 | [Safety Profile]
: Moderately toxic by
ingestion. A severe skin irritant. See also 1
DECANAL. When heated to
decomposition it emits acrid smoke and
fumes. | [Hazardous Substances Data]
112-31-2(Hazardous Substances Data) | [Toxicity]
LD50 orally in Rabbit: 3096 mg/kg LD50 dermal Rabbit 4183 mg/kg |
| Hazard Information | Back Directory | [General Description]
Colorless to light yellow liquid with a pleasant odor. Floats on water. Freezing point in 64°F. | [Reactivity Profile]
DECALDEHYDE(112-31-2) is an aldehyde. Aldehydes are frequently involved in self-condensation or polymerization reactions. These reactions are exothermic; they are often catalyzed by acid. Aldehydes are readily oxidized to give carboxylic acids. Flammable and/or toxic gases are generated by the combination of aldehydes with azo, diazo compounds, dithiocarbamates, nitrides, and strong reducing agents. Aldehydes can react with air to give first peroxo acids, and ultimately carboxylic acids. These autoxidation reactions are activated by light, catalyzed by salts of transition metals, and are autocatalytic (catalyzed by the products of the reaction). The addition of stabilizers (antioxidants) to shipments of aldehydes retards autoxidation. | [Air & Water Reactions]
Insoluble in water. | [Health Hazard]
On direct contact can produce eye and skin irritation; low general toxicity. | [Chemical Properties]
colourless liquid, an important component of citrus | [Chemical Properties]
Decanal has a penetrating, sweet, waxy, floral, citrus, pronounced fatty odor that develops a floral character on dilution
and fatty, citrus-like taste. | [Chemical Properties]
Decanal is a component
of many essential oils (e.g., neroli oil) and various citrus peel oils. It is a colorless
liquid with a strong odor, reminiscent of orange peel, which changes to a fresh
citrus odor when diluted. Decanal is used in low concentrations in blossom fragrances
(especially | [Occurrence]
Among the aliphatic aldehydes, it has the largest natural occurrence in a variety of essential oils and extraction
products: lemongrass, lavender, Taiwan citronella, sweet orange, mandarin, grapefruit, orris, coriander, Acacia farnesiana Willd.,
lemon (from different sources), bitter orange, petitgrain bergamot, petitgrain lime, lime and Bulgarian clary sage. Also reported
found in citrus peel oils and juices, apple, apricots, avocado, guava, strawberry, baked potato, tomato, rice, ginger, mozarella cheese,
other cheeses, butter, milk, lean fish, cooked chicken, beef, pork, beer, tea, cocoa, roasted peanuts, pecans, soybeans, coconut oil,
coriander seed and leaf and corn oil. | [Uses]
Decanal is used in fragrances and flavoring and it is an important component in citrus along with octanal, citral, and sinensal. It is also used in Air Care Products, Laundry and Dishwashing Products, Personal Care Products. | [Definition]
ChEBI: A fatty aldehyde formally arising from reduction of the carboxy group of capric acid (decanoic acid). | [Preparation]
Industrially prepared by oxidation of n-decanol or by reduction of the corresponding acid. | [Aroma threshold values]
Detection: 0.1 to 6 ppb; recognition: 9 ppb; aroma characteristics at 1.0%; sweet clean orange, citrus-like,
waxy and aldehydic, woody, candy-like with a floral and cilantro stem nuance. | [Taste threshold values]
Taste characteristics at 10 ppm in 5% sugar and 0.1% CA. Sweet citrus body, orange, waxy and slightly
woody with a cilantro stem and geranium floral nuance. | [Synthesis Reference(s)]
The Journal of Organic Chemistry, 32, p. 2356, 1967 DOI: 10.1021/jo01282a605
Tetrahedron Letters, 31, p. 4825, 1990 DOI: 10.1016/S0040-4039(00)97742-6 | [Flammability and Explosibility]
Nonflammable | [Chemical Reactivity]
Reactivity with Water No reaction; Reactivity with Common Materials: No reaction; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent. | [Metabolism]
See monograph on aldehyde C-8|. | [storage]
Store at -20°C |
|
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J & K SCIENTIFIC LTD.
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18210857532 18210857532 |
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https://www.jkchemical.com |
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Alfa Aesar
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http://chemicals.thermofisher.cn |
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Energy Chemical
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400-0056266 |
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www.energy-chemical.com |
| Company Name: |
jiliang chemicals
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21-62165282 |
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http://www.jiliangchem.com |
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Maya High Purity Chemicals
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+86 (573) 82222445 (0)18006601000 452520369 |
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Spectrum Chemical Manufacturing Corp.
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021-021-021-67601398-809-809-809 15221380277 |
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www.spectrumchemical.com/oa_html/index.jsp?minisite=10020&respid=22372&language=us |
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