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Capronaldehyd

Hexanal

CAS: 66-25-1

Molecular Formula: C6H12O

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Capronaldehyd - Names and Identifiers

Name Hexanal
Synonyms Hexanal
butacetin
Hexaldehyde
Hexaldethde
Capronaldehyd
Caproaldehyde
Hexanal (Capro
Capronaldehyde
n-Hexyl aldehyde
Natural Hexaldethde
HEXANAL FOR SYNTHESIS 5 ML
Capronaldehyde~Hexaldehyde
HEXANAL FOR SYNTHESIS 250 ML
n-Hexylaldehyde 〔n-Capronaldehyde〕
Hexanal (stabilised) for synthesis
CapronaldehydeHexaldehydeHexyl Aldehyde
CAS 66-25-1
EINECS 200-624-5
InChI InChI=1/C6H12O/c1-2-3-4-5-6-7/h6H,2-5H2,1H3

Capronaldehyd - Physico-chemical Properties

Molecular FormulaC6H12O
Molar Mass100.16
Density0.816g/mLat 20°C
Melting Point-56 °C
Boling Point130-131°C(lit.)
Flash Point90°F
JECFA Number92
Water Solubility4.8 g/L (20 ºC)
Solubility 6g/l
Vapor Presure10 mm Hg ( 20 °C)
Vapor Density>1 (vs air)
AppearanceLiquid
ColorClear colorless to slightly yellow
OdorPungent.
Merck14,1760
BRN506198
PH4-5 (4.8g/l, H2O, 20℃)
Storage Condition2-8°C
StabilityStable. Flammable. Incompatible with oxidizing agents, strong bases, strong reducing agents.
SensitiveAir Sensitive
Refractive Indexn20/D 1.4035(lit.)
Physical and Chemical PropertiesAlmost colorless transparent liquid, raw oil and grass gas and apple aroma. Boiling point 131 ℃, flash point 32 ℃, Freezing Point ~ 56.3 ℃. Miscible in ethanol, propylene glycol and most non-volatile oil, difficult to dissolve in water. Natural products are found in apples, strawberries, tea, bitter orange, coffee and more than ten kinds of essential oils.
UseUsed as a reagent for gas chromatography analysis

Capronaldehyd - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk CodesR10 - Flammable
R36 - Irritating to the eyes
R36/37/38 - Irritating to eyes, respiratory system and skin.
Safety DescriptionS37/39 - Wear suitable gloves and eye/face protection
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S16 - Keep away from sources of ignition.
S9 - Keep container in a well-ventilated place.
UN IDsUN 1207 3/PG 3
WGK Germany1
RTECSMN7175000
FLUKA BRAND F CODES13
TSCAYes
HS Code2912 19 00
Hazard NoteIrritant
Hazard Class3
Packing GroupIII
ToxicityLD50 orally in rats: 4.89 g/kg (Smyth)

Capronaldehyd - Reference Information

FEMA2557 | HEXANAL
olfactory Threshold 0.00028ppm
NIST chemical information information provided by: webbook.nist.gov (external link)
EPA chemical substance information information provided by: ofmpeb.epa.gov (external link)
content analysis gas chromatography analysis was performed on a polar column as GT-10-4.
toxicity GRAS(FEMA). LD50 4890 mg/kg (rat, oral).
usage limit FEMA(mg/kg): soft drinks 1.3; Cold drinks 2.8; Candy 3.6; Baked goods 4.2; pudding 2.0~2.5; Gum
Use GB 2760-96 specifies temporary use of flavorants. Mainly used for the preparation of Apple and tomato flavor.
for the synthesis of fragrances and the preparation of caproic acid. It is also used as a gas chromatography reagent.
for Wittig and Aldol reactions. It is also used as a gas chromatography reagent.
production method is obtained by oxidation of N-hexanol. In laboratory preparation, 1-bromopentane can be reacted with magnesium and then with ethyl orthoformate to give diethanol acetal. It is then distilled together with sulfuric acid and the dissociated ortho-aldehyde is distilled off simultaneously with the hydrolysis.
obtained by the reaction of calcium hexanoate and formic acid.
category flammable liquid
toxicity grade low toxicity
Acute toxicity oral-rat LD50: 4890 mg/kg; Oral-mouse LD50: 8292 mg/kg
stimulation data Skin-rabbits 500 mg/24 h mild; eye-rabbit 100 mg/24 h mild
flammability hazard characteristics flammable in case of open flame, high temperature and oxidant; combustion-induced smoke
storage and transportation characteristics The warehouse is ventilated and dried at low temperature; It is stored separately from the oxidant
extinguishing agent dry powder, dry sand, carbon dioxide, foam, 1211 extinguishing agent
spontaneous combustion temperature 220°C
toxic substance data information provided by: pubchem.ncbi.nlm.nih.gov (external link)
Last Update:2024-06-11 12:30:02
Capronaldehyd
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Capronaldehyd
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