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trans-2-Hexen-1-ol structure

trans-2-Hexen-1-ol

  • CAS:928-95-0
  • MW:100.15888
  • MF:C6H12O
 
1. Names and Identifiers
1.1 Name
trans-2-Hexen-1-ol
1.2 Synonyms
(2E)-2-Hexen-1-ol; (2E)-Heptenal; (2E)-Hex-2-en-1-ol; (e)-2-heptena; (E)-2-Hexen-1-ol; (E)-2-HEXENOL; (E)-2-hexenol,(E)-2-hexen-1-ol; (E)-2-Hexensaeure-methylester; (E)-hept-2-en-1-al; (E)-hex-2-en-1-ol; (E)-hex-2-enol; 1-Hydroxy-2-trans-hexene; 2-hexen-1-al; 2-Hexen-1-ol, (2E)-; 2-Hexen-1-ol, trans-; 2-hexen-1-one; 2-hexenaldehyde; 2-hexenyl alcohol; 2-trans-heptenal; 4-01-00-02138; EINECS 213-191-2; hept-(E)-2-enal; Hept-2(E)-enal; Hex-2-en-1-ol; HEXEN-1-OL,TRANS-2-(SG); HEXENOL TRANS-2; methyl (2E)-hex-2-enoate; methyl ester of trans-2-hexenoic acid; Methyl trans-2-hexenoate; MFCD00002927; T2 HEXENOL; TRANS 2-HEXENOL; Trans-2-Hexen-1-01; TRANS-2-HEXEN-1-OL FOR SYNTHESIS; TRANS-2-HEXEN-1-OL WITH GC; trans-2-Hexencarbonsaeuremethylester; trans-2-hexene-1-ol; trans-2-hexenoic acid methyl ester; trans-2-Hexenol; Trans-2-Hexenol(); trans-2-Hexenyl alcohol; trans-methyl 2-hexenoate; UNII-BVP79C4821;
1.3 CAS No.
928-95-0
1.4 CID
5318042
1.5 EINECS
213-191-2
1.6 Molecular Formula
C6H12O
1.7 Inchi
InChI=1S/C6H12O/c1-2-3-4-5-6-7/h4-5,7H,2-3,6H2,1H3/b5-4+
1.8 InChkey
ZCHHRLHTBGRGOT-SNAWJCMRSA-N
1.9 Canonical Smiles
CCCC=CCO
1.10 Isomers Smiles
CCC/C=C/CO
2. Properties
2.1 Appearance
Clear colorless Liquid
2.2 Storage
Ambient temperatures.
2.3 Chemical Properties
colourless liquid
2.4 Color/Form
Clear colorless
2.5 pKa
14.45±0.10(Predicted)
2.6 Water Solubility
Slightly soluble in water
2.7 Stability
Stable. Flammable. Incompatible with strong oxidizing agents, strong acids.
2.8 StorageTemp
2-8°C
3. Use and Manufacturing
3.1 Description

colourless liquid (E)-2-Hexen-1-ol occurs in many fruits and has a fruity, green odor, which is sweeter than that of the isomeric (Z)-3- hexen-1-ol and is, therefore, preferred in aroma compositions.

3.2 Methods of Manufacturing
Use Pd-CaCO3 to catalytically reduce 3-hexyn-1-ol to obtain a cis and trans mixture, which is then obtained by fractional distillation. It is obtained by reducing 2, 4-hexadienoic acid with sodium metal and ethanol.
4. Safety and Handling
4.1 Report

Reported in EPA TSCA Inventory.

4.2 Safety

Moderately toxic by ingestion. Mildly toxic by skin contact. A skin irritant. Flammable liquid when exposed to heat, sparks, or flame. When heated to decomposition it emits acrid smoke and fumes. See also ALCOHOL, DENATURED; ALCOHOLS, C6-12; ALCOHOLS, C9-11; ALCOHOLS, C12-13, ETHOXYLATED; ALCOHOLS, C12-15, ETHOXYLATED; ALCOHOLS, C12-16, ETHOXYLATED; ALCOHOLS, C14-15, ETHOXYLATED; ALCOHOLS, C16-18, ETHOXYLATED; ALCOHOLS, C8-10, ETHOXYLATED PROPOXYLATED; ALCOHOLS, C12-15, ETHOXYLATED PROPOXYLATED; ALCOHOLS, N.O.S..
Hazard Codes: IrritantXi
Risk Statements:10-36/37/38 
R10:Flammable. 
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements:26-36 
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. 
S36:Wear suitable protective clothing.
HazardClass:3

4.3 Toxicity
1.    

skn-rbt 500 mg/24H

    FCTXAV    Food and Cosmetics Toxicology. 12 (1974),911.
2.    

orl-rat LD50:3500 mg/kg

    FCTXAV    Food and Cosmetics Toxicology. 12 (1974),911.
3.    

skn-rbt LD50:4500 mg/kg

    FCTXAV    Food and Cosmetics Toxicology. 12 (1974),911.
5. MSDS

2.Hazard identification

2.1 Classification of the substance or mixture

Flammable liquids, Category 3

Skin sensitization, Category 1B

Eye irritation, Category 2

2.2 GHS label elements, including precautionary statements

Pictogram(s)
Signal word

Warning

Hazard statement(s)

H226 Flammable liquid and vapour

H317 May cause an allergic skin reaction

H319 Causes serious eye irritation

Precautionary statement(s)
Prevention

P210 Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking.

P233 Keep container tightly closed.

P240 Ground and bond container and receiving equipment.

P241 Use explosion-proof [electrical/ventilating/lighting/...] equipment.

P242 Use non-sparking tools.

P243 Take action to prevent static discharges.

P280 Wear protective gloves/protective clothing/eye protection/face protection.

P261 Avoid breathing dust/fume/gas/mist/vapours/spray.

P272 Contaminated work clothing should not be allowed out of the workplace.

P264 Wash ... thoroughly after handling.

Response

P303+P361+P353 IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water [or shower].

P370+P378 In case of fire: Use ... to extinguish.

P302+P352 IF ON SKIN: Wash with plenty of water/...

P333+P313 If skin irritation or rash occurs: Get medical advice/attention.

P321 Specific treatment (see ... on this label).

P362+P364 Take off contaminated clothing and wash it before reuse.

P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.

P337+P313 If eye irritation persists: Get medical advice/attention.

Storage

P403+P235 Store in a well-ventilated place. Keep cool.

Disposal

P501 Dispose of contents/container to ...

2.3 Other hazards which do not result in classification

none

6. NMR Spectrum
13C NMR : in CDCl3  
1H NMR : 90 MHz in CDCl3  
IR : CCl4 solution  
IR : liquid film  
Raman : 4880 A,200 M,liquid  
Mass  
7. Synthesis Route
928-95-0Total: 38 Synthesis Route
 
505-57-7
505-57-7 2 Suppliers
 
928-95-0
928-95-0 70 Suppliers
 
764-60-3
764-60-3 27 Suppliers
 
928-95-0
928-95-0 70 Suppliers
8. Precursor and Product
precursor:
product:
9. Computed Properties
10.Other Information
BRN
1719709
Chemical Properties
colourless liquid
Chemical Properties
(E)-2-Hexen-1-ol occurs in many fruits and has a fruity, green odor, which is sweeter than that of the isomeric (Z)-3- hexen-1-ol and is, therefore, preferred in aroma compositions.
Uses
trans-2-Hexen-1-ol was used to evaluate the quality of protected designation of virgin olive oils by headspace solid-phase microextraction-gas chromatography using flame ionization detection and multivariate analysis. It was also used in encapsulation of vanadium catalysts in inorganic and hybrid matrices using sol-gel method.
Storage Conditions
Use Pd-CaCO3 to catalytically reduce 3-hexyn-1-ol to obtain a cis and trans mixture, which is then obtained by fractional distillation. It is obtained by reducing 2, 4-hexadienoic acid with sodium metal and ethanol.
11. Toltal 62 Suppliers View more
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12. Related Questions
How to prepare trans-2-Hexen-1-ol and assess its toxicity?Introduction trans-2-Hexen-1-ol, referred to as 2-hexenol, is a fresh A component of the raspberry aroma, this substance has been detected in Valencian orange juice and apples and is found in nature i..
What are the applications of trans-2-Hexen-1-ol?Overview[1] trans-2-Hexen-1-ol is a volatile component found in tea. It was first discovered in tea leaves in 1966. This colorless liquid is slightly soluble in water and soluble in organic solvents s..
13. Realated Product Infomation
 
 
 
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