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Merck
CN

19190

2-丁炔-1,4-二醇

purum, ≥98.0% (GC), slightly brown

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线性分子式:
HOCH2C≡CCH2OH
化学文摘社编号:
分子量:
86.09
EC Number:
203-788-6
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1071237
MDL number:
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vapor pressure

<0.1 mmHg ( 55 °C)

grade

purum

assay

≥98.0% (GC)

color

slightly brown

bp

238 °C (lit.)

mp

53-58 °C

SMILES string

OCC#CCO

InChI

1S/C4H6O2/c5-3-1-2-4-6/h5-6H,3-4H2

InChI key

DLDJFQGPPSQZKI-UHFFFAOYSA-N

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signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1 - STOT RE 2

存储类别

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 2

flash_point_f

305.6 °F - closed cup

flash_point_c

152 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

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Małgorzata Kupczewska-Dobecka et al.
Medycyna pracy, 60(5), 347-357 (2009-12-17)
Derived No Effect Level (DNEL(inh)) has been set for occupational exposure to but-2-yno-1,4-diol according to REACH principles. Maximum allowable concentration (MAC) and DNEL(inh) have been compared. Experimental data from two inhalation studies on rats and three oral studies have been
Allergic contact dermatitis from 2-butin-1,4-diol.
V Blaschke et al.
Allergy, 56(3), 264-265 (2001-03-17)
R A Jedrychowski et al.
Journal of applied toxicology : JAT, 12(2), 117-122 (1992-04-01)
2-Butyne-1,4-diol was given to male and female Wistar Imp:DAK rats by oral gavage for 28 consecutive days in daily doses of 1, 10 or 50 mg kg-1 day-1. After 28 days all animals were necropsied. Blood samples were obtained and
Douglass F Taber et al.
The Journal of organic chemistry, 73(4), 1605-1607 (2008-01-17)
The conversion of 2-butyn-1,4-diol to (Z)-2,4-diiodobut-2-en-1-ol proceeded efficiently using in situ generated trimethylsilyl iodide. Coupling with Grignard reagents and other nucleophiles delivered (2Z)-2-iodo allylic alcohols. The geometry of the products was established by nOe.
Guy M Bernard et al.
Solid state nuclear magnetic resonance, 21(1-2), 86-104 (2002-04-13)
The alkynyl carbon chemical shift (CS) tensors for 2-butyne-1,4-diol are reported, based on analyses of the carbon-13 NMR spectra of stationary-powder and slow magic-angle spinning (MAS) samples for which the alkynyl carbon nuclei are enriched in 13C. NMR spectra of

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