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Merck
CN

721123

2-甲基-2-丁醇

anhydrous, ≥99%

别名:

tert-Amyl alcohol, 叔戊醇

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关于此项目

线性分子式:
CH3CH2C(CH3)2OH
化学文摘社编号:
分子量:
88.15
UNSPSC Code:
12352001
NACRES:
NA.21
PubChem Substance ID:
EC Number:
200-908-9
Beilstein/REAXYS Number:
1361351
MDL number:
Grade:
anhydrous
Assay:
≥99%
Bp:
102 °C (lit.)
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产品名称

2-甲基-2-丁醇, anhydrous, ≥99%

InChI

1S/C5H12O/c1-4-5(2,3)6/h6H,4H2,1-3H3

InChI key

MSXVEPNJUHWQHW-UHFFFAOYSA-N

SMILES string

CCC(C)(C)O

grade

anhydrous

vapor density

3 (vs air)

assay

≥99%

form

liquid

autoignition temp.

819 °F

expl. lim.

9 %

impurities

≤0.003% water (Karl Fischer, all unit sizes greater than 100 mL)
≤0.005% water (100 mL pkg)

evapn. residue

≤0.0005%

refractive index

n20/D 1.405 (lit.)

pH

6.0 (20 °C, 118 g/L)

bp

102 °C (lit.)

mp

−12 °C (lit.)

density

0.805 g/mL at 25 °C (lit.)

Quality Level

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Application

叔戊醇作为有机溶剂 化学中间体 可用于汽油燃料添加剂 、食品香精 、医药 过氧酯、油墨成分和橡胶生产中的稳定剂。

signalword

Danger

Hazard Classifications

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

target_organs

Central nervous system, Respiratory system

存储类别

3 - Flammable liquids

wgk

WGK 1

flash_point_f

68.9 °F - closed cup

flash_point_c

20.5 °C - closed cup

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Chen, C.-X., Wu, Q.
Enz. Microbiol. Technol., 42, 601-601 (2008)
Torsten Weil et al.
Organic letters, 10(8), 1513-1516 (2008-03-28)
We present a mild and efficient method for the completely regioselective alcoholysis of styrene oxides utilizing a cooperative Brønsted acid-type organocatalytic system comprised of mandelic acid (1 mol %) and N,N'-bis-[3,5-bis-(trifluoromethyl)phenyl]-thiourea (1 mol %). Various styrene oxides are readily transformed
Teai, T.; Claude-Lafontaine, A. et al.
J. Essent. Oil Res., 13, 314-314 (2001)
Funk, R.L.; Daily, W.J.; Parvez, D.M.
The Journal of Organic Chemistry, 53, 4143-4143 (1998)
Jiang-Ning Hu et al.
Journal of agricultural and food chemistry, 56(22), 10988-10993 (2008-11-06)
In the lipase (Novozyme 435)-catalyzed synthesis of ginsenoside Rb1 esters, different acyl donors were found to affect not only the degree of conversion but also the regioselectivity. The reaction of acyl donors with short carbon chain was more effective, showing

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