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Sigma-Aldrich

1,2-Dichloropropane

99%

Sinónimos:

Propylene dichloride

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About This Item

Fórmula lineal:
CH3CHClCH2Cl
Número de CAS:
78-87-5
Peso molecular:
112.99
Beilstein/REAXYS Number:
1718880
EC Number:
201-152-2
MDL number:
MFCD00000868
UNSPSC Code:
12352100
PubChem Substance ID:
329769241
NACRES:
NA.22

vapor density

3.89 (vs air)

vapor pressure

40 mmHg ( 19.4 °C)

assay

99%

form

liquid

autoignition temp.

1035 °F

expl. lim.

14.5 %

refractive index

n20/D 1.439 (lit.)
n20/D 1.439

bp

95-96 °C (lit.)

mp

−100 °C (lit.)

density

1.156 g/mL at 25 °C (lit.)

SMILES string

CC(Cl)CCl

InChI

1S/C3H6Cl2/c1-3(5)2-4/h3H,2H2,1H3

InChI key

KNKRKFALVUDBJE-UHFFFAOYSA-N

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Categorías relacionadas

Application

1,2-Dichloropropane can be used as a building block to synthesize:
  •  2-Ylidene-1,3-dithiolane derivatives via one-pot reaction with carbon disulfide and active methylene compounds in the presence of sodium ethylate.      
  • β-Chloropropylsulfurs by controllable dechloro-coupling reaction with thiols.      
  • Thiazolidine and 1,3-thiazinane derivatives via [3+2] and [3+3] annulation reaction with β-ketothioamides in the presence of phosphonium ylide as a catalyst.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 1B - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

59.0 °F - closed cup

flash_point_c

15.0 °C - closed cup

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
BCCM4590
BCCM0625
BCCM5152
BCCK0482
BCBZ4348

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Synthesis of some 2-ylidene-1, 3-dithiolanes
Lipin KV, et al.
Russ. J. Org. Chem., 53(1), 147-149 (2017)
Monish Arbaz Ansari et al.
Organic & biomolecular chemistry, 17(41), 9151-9162 (2019-10-09)
Phosphonium ylides are being reported here as a catalyst for the formation of thiazolidines and 1,3-thiazinanes from β-ketothioamides (which act as a three atom N, C, and S synthon) with dihaloalkanes via [3 + 2] and [3 + 3] annulations
Divergent Electrolysis for the Controllable Coupling of Thiols with 1, 2-Dichloroethane: a Mild Approach to Sulfide and Sulfoxide
Ling F, et al.
Green Chemistry (2022)
Kirsti M Ritalahti et al.
Applied and environmental microbiology, 70(7), 4088-4095 (2004-07-09)
1,2-Dichloropropane (1,2-D), a widespread groundwater contaminant, can be reductively dechlorinated to propene by anaerobic bacteria. To shed light on the populations involved in the detoxification process, a comprehensive 16S rRNA gene-based bacterial community analysis of two enrichment cultures derived from
A Trevisan et al.
Archives of toxicology, 66(9), 641-645 (1992-01-01)
Sex- and age-related nephrotoxicity due to 1,2-dichloropropane was studied in vitro by means of renal cortical slices obtained from Wistar rats. Reduced glutathione content, organic anion accumulation (p-aminohippurate), and release of malondialdehyde (to measure the extent of lipid peroxidation), aspartate
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