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| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 5 mL | Please contact Customer Service for Availability | CZK 3,060.00 | |
| 25 mL | Please contact Customer Service for Availability | CZK 6,490.00 |
About This Item
Linear Formula:
CH3(CH2)5OH
CAS Number:
Molecular Weight:
102.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-852-3
Beilstein/REAXYS Number:
969167
MDL number:
Assay:
≥99.5% (GC)
vapor density
4.5 (vs air)
Quality Segment
vapor pressure
1 mmHg ( 25.6 °C)
product line
ReagentPlus®
assay
≥99.5% (GC)
autoignition temp.
559 °F
refractive index
n20/D 1.418
bp
156-157 °C (lit.)
mp
−52 °C (lit.)
density
0.814 g/mL at 25 °C (lit.)
functional group
hydroxyl
SMILES string
CCCCCCO
InChI
1S/C6H14O/c1-2-3-4-5-6-7/h7H,2-6H2,1H3
InChI key
ZSIAUFGUXNUGDI-UHFFFAOYSA-N
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
140.0 °F - closed cup
flash_point_c
60 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Caimeng Zhang et al.
Food chemistry, 333, 127469-127469 (2020-07-17)
The dominant volatile off-flavor compounds of pea and soy milk were investigated by gas chromatography-olfactometry-mass spectrometry (GC-O-MS), sensory evaluation, and odor-activity values (OAVs), which led to the identification of their differences. We identified 11 aroma compounds as important odorants with
Leandro Dias Araujo et al.
Food research international (Ottawa, Ont.), 98, 79-86 (2017-06-15)
Elemental sulfur is a fungicide traditionally used to control Powdery Mildew in the production of grapes. The presence of sulfur residues in grape juice has been associated with increased production of hydrogen sulfide during fermentation, which could take part in
Justin T Mohr et al.
Journal of medicinal chemistry, 48(12), 4172-4176 (2005-06-10)
The polyhydroxyalkanes 1,6,11,16-hexadecanetetraol (1) and 2,7,12,17-octadecanetetraol (2) were synthesized utilizing the thiophene ring as a scaffold to affix the hydroxyalkyl chains by lithiation of the acidic alpha-hydrogens and subsequent desulfurization. Both compounds exhibited significant anesthetic potency, individually and in additivity
Global Trade Item Number
| SKU | GTIN |
|---|---|
| CDS019959-100MG | 04061828951857 |
| 52828-25ML | 04061837015519 |
| 52828-5ML | 04061837015526 |

