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Merck
CN

150045

2,4-Dimethyl-3-pentanol

99%

Synonym(s):

Diisopropylcarbinol

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About This Item

Linear Formula:
(CH3)2CHCH(OH)CH(CH3)2
CAS Number:
600-36-2
Molecular Weight:
116.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24849002
EC Number:
209-993-7
Beilstein/REAXYS Number:
1731593
MDL number:
MFCD00008921
Assay:
99%

Key Documents

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Product Name

2,4-Dimethyl-3-pentanol, 99%

InChI key

BAYAKMPRFGNNFW-UHFFFAOYSA-N

InChI

1S/C7H16O/c1-5(2)7(8)6(3)4/h5-8H,1-4H3

SMILES string

CC(C)C(O)C(C)C

assay

99%

refractive index

n20/D 1.425 (lit.)

bp

139-140 °C (lit.)

density

0.829 g/mL at 25 °C (lit.)

functional group

hydroxyl

Quality Level

100

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Application

2,4-Dimethyl-3-pentanol was used as a proton source in the diastereoselective coupling with 2-substituted acrylate derivatives. It was used in the polymerization of 1,1′-(1,3-phenylene) diethanol (1,3-diol) and diisopropyl adipate.

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

98.6 °F - closed cup

flash_point_c

37 °C - closed cup

ppe

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

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
06115JA
05324AY
19010TA
12021CQ
10628EQ

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Bart A C van As et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 13(29), 8325-8332 (2007-07-31)
The well-known dynamic kinetic resolution of secondary alcohols and esters was extended to secondary diols and diesters to afford chiral polyesters. This process is an example of iterative tandem catalysis (ITC), a polymerization method where the concurrent action of two
Hegui Gong et al.
Organic letters, 11(4), 879-882 (2009-01-28)
A mild, stereoselective method for the Ni-catalyzed synthesis of alpha-C-alkylglycosides is reported. This approach entails the reductive coupling of glycosyl bromides with activated alkenes at room temperature, with low alkene loading as an important feature. Diastereoselective coupling with 2-substituted acrylate
Liping Wang et al.
Pesticide biochemistry and physiology, 139, 46-52 (2017-06-10)
Camptothecin (CPT), a quinolone alkaloid extracted from Camptotheca acuminata Decne, exhibits potential insecticidal activities against various insect species. Our previous studies have showed that CPT induced apoptosis in Spodoptera exigua Hübner cell line and inhibited the relaxation activity of topoisomerase

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