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270679

1-Butanol

suitable for HPLC, 99.8%

Synonym(s):

n-Butanol, Butyl alcohol

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About This Item

Linear Formula:
CH3(CH2)3OH
CAS Number:
71-36-3
Molecular Weight:
74.12
EC Number:
200-751-6
UNSPSC Code:
12190000
PubChem Substance ID:
329752962
Beilstein/REAXYS Number:
969148
MDL number:
MFCD00002964
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vapor density

2.55 (vs air)

vapor pressure

5 (4 mmHg) at 20 °C hPa

assay

99.8%

form

liquid

autoignition temp.

649 °F

purified by

glass distillation

expl. lim.

11.2 %

technique(s)

HPLC: suitable

impurities

<0.030% water

evapn. residue

<0.0005%

color

colorless

refractive index

n20/D 1.399 (lit.)

bp

116-118 °C (lit.), 117.7 °C

mp

−90 °C (lit.)

density

0.81 g/mL at 25 °C (lit.)

λ

H2O reference

UV absorption

λ: 215 nm Amax: 1.00, λ: 220 nm Amax: 0.50, λ: 240 nm Amax: 0.10, λ: 260 nm Amax: 0.04, λ: 280-400 nm Amax: 0.01

SMILES string

CCCCO

InChI

1S/C4H10O/c1-2-3-4-5/h5H,2-4H2,1H3

InChI key

LRHPLDYGYMQRHN-UHFFFAOYSA-N

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signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Central nervous system, Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

95.0 °F - Pensky-Martens closed cup

flash_point_c

35 °C - Pensky-Martens closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
03915LV
00629CX
05818KW
U14821
03045KC

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Prasenjit Seal et al.
The journal of physical chemistry. A, 117(2), 275-282 (2012-12-19)
In the present work, we study the H atom abstraction reactions by hydroxyl radical at all five sites of 1-butanol. Multistructural variational transition state theory (MS-VTST) was employed to estimate the five thermal rate constants. MS-VTST utilizes a multifaceted dividing
A L Gainer et al.
Clinica chimica acta; international journal of clinical chemistry, 123(1-2), 11-17 (1982-08-04)
Neutrophils were isolated in good yield from fresh whole blood and their alkaline phosphatase was solubilized. Inhibitor studies using L-phenylalanylglycylglycine, L-phenylalanine and L-homoarginine revealed a distinct pattern of inhibition for each of the crude or purified preparations of the human
Joel G Davis et al.
Nature, 491(7425), 582-585 (2012-11-23)
Hydrophobic hydration is considered to have a key role in biological processes ranging from membrane formation to protein folding and ligand binding. Historically, hydrophobic hydration shells were thought to resemble solid clathrate hydrates, with solutes surrounded by polyhedral cages composed
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