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Hexan-1-ol

n-Hexanol

CAS: 111-27-3

Molecular Formula: C6H14O

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Hexan-1-ol - Names and Identifiers

Name n-Hexanol
Synonyms epal6
Epal 6
1-hexanol
n-Hexanol
Hexan-1-ol
Alcohol C-6
Amyl carbinol
Hexyl Alcohol
1-Hexylalcohol
caproylalcohol
n-Hexyl Alcohol
Caproyl alcohol
Caproic alcohol
Capronicalcohol
1-Hexyl alcohol
alcooln-hexylique
Natural Hexyl Alcohol
Hexyl Alcohol(Alcohol C-6)
CAS 111-27-3
EINECS 203-852-3
InChI InChI=1/C6H14O/c1-2-3-4-5-6-7/h7H,2-6H2,1H3

Hexan-1-ol - Physico-chemical Properties

Molecular FormulaC6H14O
Molar Mass102.17
Density0.814 g/mL at 25 °C (lit.)
Melting Point-52 °C (lit.)
Boling Point156-157 °C (lit.)
Flash Point140°F
JECFA Number91
Water Solubility6 g/L (25 ºC)
Solubility ethanol: soluble(lit.)
Vapor Presure1 mm Hg ( 25.6 °C)
Vapor Density4.5 (vs air)
AppearanceLiquid
ColorClear colorless
OdorSweet; mild.
Merck14,4697
BRN969167
pKa15.38±0.10(Predicted)
Storage Conditionno restrictions.
StabilityStable. Substances to be avoided include strong acids, strong oxidizing agents. Combustible.
Explosive Limit1.2-7.7%(V)
Refractive Indexn20/D 1.418(lit.)
Physical and Chemical PropertiesColorless liquid. Boiling point 157 ℃, the relative density of 0.819, and ethanol, propylene glycol, oil can be miscible with each other. There are light green tender branches and leaves of breath, micro-band wine, fruit and fat flavor. N-hexanol or a carboxylic acid ester thereof is present in trace amounts in citrus, berries, and the like. Tea and sesame leaf oil a variety of lavender oil, banana, apple, strawberry, violet leaf oil and other essential oils are also contained.
UseFor the production of surfactants, plasticizers, fatty alcohols, etc

Hexan-1-ol - Risk and Safety

Hazard SymbolsXn - Harmful
Harmful
Risk Codes22 - Harmful if swallowed
Safety Description24/25 - Avoid contact with skin and eyes.
UN IDsUN 2282 3/PG 3
WGK Germany1
RTECSMQ4025000
TSCAYes
HS Code29051900
Hazard Class3
Packing GroupIII
ToxicityLD50 oral in rat: 720mg/kg

Hexan-1-ol - Upstream Downstream Industry

Downstream Productsgamma-nonanoic lactone

Hexan-1-ol - Nature

Open Data Verified Data

with fruit aroma, a little green leaf breath. Soluble in water and a variety of organic solvents.

Last Update:2024-01-02 23:10:35

Hexan-1-ol - Preparation Method

Open Data Verified Data

obtained by acid reduction.

Last Update:2022-01-01 10:08:05

Hexan-1-ol - Use

Open Data Verified Data

is widely used in the preparation of flavors. Mainly used for the preparation of coconut and berry flavor. Usually, 0. 22~18mg/kg is used for food flavor. It is used as soap essence, detergent essence, perfume essence, cream essence, etc.

Last Update:2022-01-01 10:08:05

Hexan-1-ol - Safety

Open Data Verified Data

rat acute oral LD50 4.59-4. 87g/kg, rabbit percutaneous LD50 is 3. IML/kg and more than 5 g/kg. In the closed condition, the sample was applied to the skin of the rabbit for 1 day, and moderate irritation was observed. The Vaseline preparation with concentration of 1% was subjected to a two-day closed skin contact test on human body, and no irritation and sensitization were found.

Last Update:2022-01-01 10:08:06

Hexan-1-ol - Reference Information

FEMA2567 | HEXYL ALCOHOL
relative polarity 0.559
olfactory Threshold 0.006ppm
LogP1.8
NIST chemical information information provided by: webbook.nist.gov (external link)
EPA chemical substance information information provided by: ofmpeb.epa.gov (external link)
Use n-hexanol is used for flavor-based and formulation of essential oils (such as Geranium oil) as part of the head fragrance, and can also be used in trace amounts for Violet, osmanthus fragrans, Magnolia, ylang ylang type essence, to modify or increase the green and tender breath, can also be used in trace amounts of edible coconut formula, berries and all kinds of fruit flavor; Used as solvent and Analytical reagents, also used in the pharmaceutical industry for the preparation of preservatives and sleeping pills. The product is China's GB2760-86 provisions to allow the use of edible spices, mainly for the preparation of coconut and berry flavor; For the production of surfactants, plasticizers, fatty alcohols; Used as chromatographic analysis reagents, also used in organic synthesis, etc.
GB 2760-96 provides for the permitted use of flavorants. Commonly used in the essence base and the preparation of essential oils (such as leaf oil) as part of the head fragrance, can also be used in trace amounts of violet, osmanthus, Magnolia, ylang-ylang type essence, to modify or increase the green and tender breath, can also be used in trace amounts of coconut formula, berries and all kinds of fruit flavor.
gas chromatographic analysis standard. Lithium chloride was separated from potassium chloride and sodium chloride. Solvent.
content analysis 700 of freshly distilled pyridine is placed in a 1000 brown vial with a glass stopper, 11 5g of phthalic anhydride was added and shaken strongly until completely dissolved. Take 25.0 of this solution, put it into an appropriate heat-resistant, pressure-resistant bottle, tightly wrapped and fixed outside the bottle. Accurately weigh about 1 g of the sample with a weighing pipette, put it into a pressure bottle, and cover it. It was wrapped and fixed in a canvas bag, heated in a water bath at 98-100 ° C. For 3H, and the liquid level in the water bath was higher than that in the bottle. After removal, it was cooled to room temperature, and the stopper was carefully opened so that the contents were not lost. Add 0.5 ml of 50.0 mol/L sodium hydroxide solution to the bottle (note: This 50.0ml of 0.5 mol/L sodium hydroxide solution is not included in the final calculation), add 5 drops of 1% phenolphthalein pyridine solution, then titrate to pink end point with 0.5 mol/L sodium hydroxide solution and keep it unchanged for 15 s. A blank test was also performed. Each ml of 0.5mol/L sodium hydroxide solution is equivalent to 51.09 mg of hexanol (C6 H14O). Or according to the GT-10-4 gas chromatography non-polar column method.
toxicity GRAS(FEMA). LD50 720 mg/kg (rat, oral).
usage limit FEMA(mg/kg): Soft drink 6.6; Cold drink 26; Candy 21; Baked goods 18; pudding 0.22~0.28. Moderate limits (FDA § 172.515,2000).
production method is obtained by reduction of N-hexanoic acid.
industrially, it is generally obtained by reduction of acetic acid. In laboratory preparation, butyl magnesium bromide can be obtained by the reaction of butyl bromide with magnesium chip, and then reacted with ethylene oxide to obtain ethanol.
category flammable liquid
toxicity grade poisoning
Acute toxicity oral-rat LD50:720 mg/kg; Oral-mouse LD50:1950 mg/kg
stimulation data Skin-rabbits 10 mg/24 h mild; eye-rabbit 250 μg severe
flammability hazard characteristics flammable in open flame, high temperature, strong oxidant; combustion emissions
storage and transportation characteristics The package is complete, light and light unloading; The warehouse is ventilated, away from open flame, high temperature, separate from oxidant
fire extinguishing agent foam, dry powder, carbon dioxide, sand
spontaneous combustion temperature 559 ° F.
toxic substance data information provided by: pubchem.ncbi.nlm.nih.gov (external link)
Last Update:2024-04-09 20:52:54
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View History
Hexan-1-ol
联苯酚羧酸甲酯
Thiocyanic acid, 1,4-dihydro-4-imino-1-methyl-2-pyrimidinyl ester (9CI)
1-methylnicotinamide chloride
2-anilinoisonicotinonitrile
Ethylene glycol monethyl ether acetate
AKOS PAO-0343
Octacide 264
Α-D-吡喃葡萄糖酰氟
n-Butyldi(tert-butyl)phosphonium tetrafluoroborate
Downstream Products for Hexan-1-ol
gamma-nonanoic lactone
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