1-Chloropentane

[ Density]:
0.9±0.1 g/cm3

[ Boiling Point ]:
107.2±3.0 °C at 760 mmHg

[ Melting Point ]:
-60 °C

[ Molecular Formula ]:
C₅H₁₁Cl

[ Molecular Weight ]:
106.594

[ Flash Point ]:
11.1±0.0 °C

[ Exact Mass ]:
106.054932

[ LogP ]:
3.10

[ Vapour Pressure ]:
32.0±0.2 mmHg at 25°C

[ Index of Refraction ]:
1.406

[ Water Solubility ]:
practically insoluble

Click to get detail MSDS

[ Symbol ]:

GHS02, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H225-H302 + H312 + H332

[ Precautionary Statements ]:
P210-P280

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
F:Flammable;Xn:Harmful;

[ Risk Phrases ]:
R11;R20/21/22

[ Safety Phrases ]:
S9-S29

[ RIDADR ]:
UN 1107 3/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
II

[ Hazard Class ]:
3

[ HS Code ]:
2903199000

Precursor

DownStream

[ HS Code ]: 2903199000

[ Summary ]:
2903199000 other saturated chlorinated derivatives of acyclic hydrocarbons。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%

QSPR modeling of octanol/water partition coefficient for vitamins by optimal descriptors calculated with SMILES.

Eur. J. Med. Chem. 43 , 714-40, (2008)

Simplified molecular input line entry system (SMILES) has been utilized in constructing quantitative structure-property relationships (QSPR) for octanol/water partition coefficient of vitamins and org...

Stereo-isomerism controls surface reactivity: 1-chloropentane-pairs on Si(100)-2×1.

Chem. Commun. (Camb.) 47(44) , 12101-3, (2011)

Chloropentane forms asymmetric ('A') and symmetric ('S') pairs on Si(100)-2×1, differing in the direction of curvature of one pentane tail. Surprisingly this renders the rate of thermal reaction of 'A...

Kinetic study on reactions between polymer chain-ends. Coupling reactions of living polystyrene with chloro-ended polystyrene. Okamoto A, et al.

Eur. Polymer J. 18(6) , 545-48, (1982)

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