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Merck
CN

W510254

2-丁醇

99%

别名:

(±)-2-丁醇, 仲丁醇

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关于此项目

线性分子式:
CH3CH2CH(OH)CH3
化学文摘社编号:
分子量:
74.12
UNSPSC Code:
12164502
Flavis number:
2.121
PubChem Substance ID:
EC Number:
201-158-5
Beilstein/REAXYS Number:
773649
MDL number:
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biological source

synthetic

vapor density

2.6 (vs air)

vapor pressure

12.5 mmHg ( 20 °C)

assay

99%

autoignition temp.

761 °F

expl. lim.

9.8 %

refractive index

n20/D 1.397 (lit.)

bp

98 °C (lit.)

mp

−115 °C (lit.)

density

0.808 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

SMILES string

CCC(C)O

InChI

1S/C4H10O/c1-3-4(2)5/h4-5H,3H2,1-2H3

InChI key

BTANRVKWQNVYAZ-UHFFFAOYSA-N

Other Notes

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pictograms

FlameExclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - STOT SE 3

target_organs

Central nervous system, Respiratory system

存储类别

3 - Flammable liquids

wgk

WGK 1

flash_point_f

80.6 °F - closed cup

flash_point_c

27 °C - closed cup

ppe

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

法规信息

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Lot/Batch Number

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Stefan Hofbauer et al.
Archives of biochemistry and biophysics, 574, 36-48 (2015-01-21)
Chlorite dismutase-like proteins are structurally closely related to functional chlorite dismutases which are heme b-dependent oxidoreductases capable of reducing chlorite to chloride with simultaneous production of dioxygen. Chlorite dismutase-like proteins are incapable of performing this reaction and their biological role
Prabha Dwivedi et al.
Analytical chemistry, 78(24), 8200-8206 (2006-12-15)
This article introduces the concept of chiral ion mobility spectrometry (CIMS) and presents examples demonstrating the gas-phase separation of enantiomers of a wide range of racemates including pharmaceuticals, amino acids, and carbohydrates. CIMS is similar to traditional ion mobility spectrometry
Robert Brosnan et al.
Anesthesia and analgesia, 103(1), 86-91 (2006-06-23)
Chirality has been proposed as a means for distinguishing relevant from irrelevant molecular targets of action, but the sensitivity and specificity of this test is unknown for volatile anesthetics. We applied enantiomers of two chiral anesthetic alcohols (2-butanol and 2-pentanol)