2-Chloropropane supplier

Name
Isopropyl chloride
EINECS 200-858-8
CAS No. 75-29-6
Article Data189
CAS DataBase
Density 0.874 g/cm³
Solubility 3.1 g/L (20 °C) in water
Melting Point -118 °C
Formula C₃H₇Cl
Boiling Point 37.254 °C at 760 mmHg
Molecular Weight 78.5416
Flash Point -35 °C
Transport Information UN 2456 3/PG 1
Appearance colorless liquid with pleasant smells
Safety 9-29
Risk Codes 12-36/37-20/21/22-11
Molecular Structure
Hazard Symbols F+, Xi, Xn, F
Synonyms 2-Propyl chloride;Chlorodimethylmethane;Isoprid;Isopropyl chloride;Propane, 2-chloro-;Narcosop;R 280da;
PSA 0.00000
LogP 1.63360

Synthetic route

: 67-63-0
isopropyl alcohol

: 75-29-6
isopropyl chloride

Conditions

Conditions	Yield
With indium(III) chloride; dimethylmonochlorosilane; benzil In dichloromethane at 20℃; for 6h;	100%
With priphenylchlorophosphonium phosphorodichloridate at 20℃; Arbuzov reaction;	84%
With hydrogenchloride at 120℃; under 7500.75 Torr; Flow reactor;	54%

: 74-93-1
methylthiol

: 1912-24-9
6-chloro-N-ethyl-N'-isopropyl-1,3,5-triazine-2,4-diamine

A: 75-29-6
isopropyl chloride

B: 834-12-8
ametryn

Conditions

Conditions	Yield
With ZSM-5 In isopropyl alcohol at 90 - 110℃; under 3675.37 - 5850.59 Torr; for 1h; Temperature; Pressure; Reagent/catalyst; Sealed tube;	A 70.91 g B 99.9%

...Expand

: isopropyl o-(N-methylcarbamoyl)phenyl sulphoxide

A: 2527-66-4
2-methyl-1,2-benzisothiazole-3(2H)-one

B: 75-29-6
isopropyl chloride

Conditions

Conditions	Yield
With thionyl chloride In tetrachloromethane for 2h; Heating;	A 99% B n/a

: 143885-03-4
isopropyloxy(diphenyl)-λ6-sulfanenitrile

A: 75-29-6
isopropyl chloride

B: 22731-83-5
S,S-diphenylsulphoximine

Conditions

Conditions	Yield
With hydrogenchloride In [D3]acetonitrile at 20℃; for 0.25h;	A 99% B n/a

: 110-86-1
pyridine

: Cl2Pt(C(OiPr)(Me))2

A: 75-29-6
isopropyl chloride

B: 1395411-06-9
cis-Cl(py)Pt(COMe)[C(OiPr)(Me)]

C: 67-63-0
isopropyl alcohol

Conditions

Conditions	Yield
In tetrahydrofuran-d8 at 55℃; for 21h;	A n/a B 98% C n/a

...Expand

: 187737-37-7
propene

: 75-29-6
isopropyl chloride

Conditions

Conditions	Yield
With hydrogenchloride; chromium; silica gel at 140℃; Product distribution; Rate constant; oth. temperature, oth. catalysts, E(activ.);	95%
With hydrogenchloride; aluminium oxide, chlorided at 40 - 60℃; under 759.826 - 1519.65 Torr; for 200h;	94%
With hydrogenchloride; aluminium oxide, fluorided for 200h;	94%

: 56-23-5
tetrachloromethane

: 80937-33-3
oxygen

: 1071-39-2
diisopropylmercury

A: 74-98-6
propane

B: 75-29-6
isopropyl chloride

C: 67-66-3
chloroform

D: 30615-19-1
isopropylmercury(II) chloride

E: mercury

Conditions

Conditions	Yield
In neat (no solvent) 20°C, 96 h; further products;	A 4% B 48% C 30% D 95% E 5%

...Expand

: 108-20-3
di-isopropyl ether

: 75-29-6
isopropyl chloride

Conditions

Conditions	Yield
With tin(IV) chloride In dichloromethane at 110℃; for 60h; sealed tube; Inert atmosphere;	95%
With titanium tetrachloride In dichloromethane at 150℃; for 60h;

: 67-63-0
isopropyl alcohol

A: 1809-20-7
diisopropyl hydrogenphosphonate

B: 75-29-6
isopropyl chloride

Conditions

Conditions	Yield
With phosphorus trichloride at 0 - 50℃; for 50h;	A 94% B n/a

: 187737-37-7
propene

A: 557-98-2
2-chloropropene

B: 26198-63-0, 78-87-5
1,2-Dichloropropane

C: 542-75-6
E/Z-1,3-Dichloropropene

D: 75-29-6
isopropyl chloride

E: 590-21-6
propenyl chloride

F: 107-05-1
3-chloroprop-1-ene

Conditions

Conditions	Yield
With aluminum oxide; copper dichloride; dibenzoyl peroxide at 489.9℃; for 0.000555556h; Product distribution; Mechanism; also other temperatures (503 K - 753 K) and initiators (chloral dioxyperoxide);	A 0.7% B 3.3% C 0.8% D 1.8% E 0.9% F 91.4%

...Expand

: 56-23-5
tetrachloromethane

: 1071-39-2
diisopropylmercury

A: mercury(I) chloride

B: 75-29-6
isopropyl chloride

C: 67-66-3
chloroform

D: 30615-19-1
isopropylmercury(II) chloride

E: mercury

Conditions

Conditions	Yield
In neat (no solvent) 130°C, 10 h; further products;	A 3% B 51% C 50% D 91% E 3%

...Expand

: 116-17-6
triisopropyl phosphite

: 40510-88-1
1-acetoxy-2-chloromethoxyethane

A: 75-29-6
isopropyl chloride

B: 162612-58-0
diisopropyl <(2-acetoxyethoxy)methyl>phosphonate

Conditions

Conditions	Yield
at 110℃; for 3h; Inert atmosphere;	A n/a B 90%

...Expand

: 1,4-diisopropylcyclohexa-2,5-diene-1,4-dicarboxylic acid

A: 75-29-6
isopropyl chloride

B: 536-66-3
4-Isopropylbenzoic acid

Conditions

Conditions	Yield
With chlorosulfonic acid In dichloromethane at 0℃;	A n/a B 84%

: 67-63-0
isopropyl alcohol

A: 75-29-6
isopropyl chloride

B: 691-96-3
diisopropyl phosphite

Conditions

Conditions	Yield
With zinc(II) phosphide; oxygen; copper dichloride at 50℃; under 750.06 Torr; Title compound not separated from byproducts;	A n/a B 82.3%
With zinc(II) phosphide; oxygen; copper dichloride at 50℃; Kinetics;

: 67-63-0
isopropyl alcohol

A: 1499-17-8
o-phenylene chlorophosphate

B: 75-29-6
isopropyl chloride

Conditions

Conditions	Yield
With CPT	A n/a B 74%

: 74-98-6
propane

: 75-29-6
isopropyl chloride

Conditions

Conditions	Yield
With dichloromethane; antimony pentafluoride at -78 - 20℃; Product distribution; Mechanism; other alkanes and cycloalkanes; methylene bromide;	69%
With dichloromethane; antimony pentafluoride 1.) -78 deg C, 2 h, 2.) RT, 24 h;	69%
In various solvent(s) at -158.1℃; Kinetics; Irradiation;

: 79-30-1
isobutyryl chloride

A: 513-37-1
2-methylprop-1-enyl chloride

B: 75-29-6
isopropyl chloride

Conditions

Conditions	Yield
With pyrographite at -196.16℃; under 1E-05 - 0.0001 Torr;	A 66% B 34%

: 2176-62-7
2,3,4,5,6-pentachloropyridine

: 116-17-6
triisopropyl phosphite

A: 75-29-6
isopropyl chloride

B: 87361-54-4
2,3,5,6-Tetrachlor-4-pyridylphosphonsaeure-diisopropylester

Conditions

Conditions	Yield
at 130℃; for 16h;	A n/a B 60%

...Expand

: 116-17-6
triisopropyl phosphite

: 57182-16-8
2,2,2-trichloro-N-methylacetimidoyl chloride

A: 75-29-6
isopropyl chloride

B: 70795-54-9
C15H31Cl2NO6P2

Conditions

Conditions	Yield
In toluene for 2h; Heating;	A n/a B 56%

...Expand

: 116-17-6
triisopropyl phosphite

: 57182-25-9
N-ethyl-2,2,2-trichloro-acetimidoyl chloride

A: 75-29-6
isopropyl chloride

B: 70795-58-3
{2,2-Dichloro-1-[(diisopropoxy-phosphoryl)-ethyl-amino]-vinyl}-phosphonic acid diisopropyl ester

Conditions

Conditions	Yield
In toluene for 2h; Heating;	A n/a B 51%

...Expand

: 187737-37-7
propene

: 75-09-2
dichloromethane

A: 75-29-6
isopropyl chloride

B: 1190-22-3
1,3-dichlorobutane

C: 616-19-3
1,3-dichloro-2-methylpropane

Conditions

Conditions	Yield
With RhCl(PPh3)3 at 200℃; for 3h;	A 50% B 23% C 15%

...Expand

: 187737-37-7
propene

: 67-66-3
chloroform

A: 75-29-6
isopropyl chloride

B: 66675-32-9
1,1,2-trichloro-butane

C: 62108-65-0
1,1,3-trichloro-2-methyl-propane

Conditions

Conditions	Yield
With RhCl(PPh3)3 at 200℃; for 3h;	A 46% B 20% C 12%

...Expand

: C9H21ClO3P(1+)*C2Cl2N(1-)

A: 75-29-6
isopropyl chloride

B: triisopropyl (trichlorovinyl)phosphorimidate

Conditions

Conditions	Yield
at 170℃; under 0.03 Torr;	A 20% B 31%
at 165 - 170℃; under 0.03 Torr; Product distribution;

: 594-20-7
2,2-dichloropropane

A: 563-79-1
2,3-Dimethyl-2-butene

B: 557-98-2
2-chloropropene

C: 75-29-6
isopropyl chloride

Conditions

Conditions	Yield
With iron pentacarbonyl at 140℃; for 3h; Product distribution; various reaction conditions;	A 8% B 5% C 16%

...Expand

: 71-23-8
propan-1-ol

A: 540-54-5
1-Chloropropane

B: 75-29-6
isopropyl chloride

Conditions

Conditions	Yield
With hydrogenchloride; aluminum oxide at 420℃;

: 75-30-9
2-iodo-propane

: 75-29-6
isopropyl chloride

Conditions

Conditions	Yield
With mercury dichloride

: 56-23-5
tetrachloromethane

: 74-98-6
propane

: 110-05-4
di-tert-butyl peroxide

: 75-29-6
isopropyl chloride

Conditions

Conditions	Yield
at 140℃;

...Expand

: 56-23-5
tetrachloromethane

: 74-98-6
propane

: 110-05-4
di-tert-butyl peroxide

A: 75-29-6
isopropyl chloride

B: 67-66-3
chloroform

Conditions

Conditions	Yield
at 138℃;

...Expand

: 56-23-5
tetrachloromethane

: 3437-84-1
isobutyroyl peroxide

A: 75-29-6
isopropyl chloride

B: 67-72-1
hexachloroethane

...Expand

: 98070-46-3
trichlorophosphoranylidene-carbamic acid isopropyl ester

A: 870-30-4
isocyanatophosphonic dichloride

B: 75-29-6
isopropyl chloride

Conditions

Conditions	Yield
Zersetzt;

: 75-29-6
isopropyl chloride

: 1000993-74-7
1-(4-isopropyl-5-methyl-2-furyl)propan-1-one

Conditions

Conditions	Yield
Stage #1: 5-methyl-2-propionylfuran; aluminum (III) chloride at 0 - 30℃; for 0.5h; Stage #2: isopropyl chloride at 0 - 10℃;	100%

: 1020552-35-5, 59461-43-7, 103364-89-2
(1R,4S,8R,11S)-(1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane)nickel(I)

: 75-29-6
isopropyl chloride

: 103258-96-4
(1R,4S,8R,11S)-(1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane)(2-propyl)nickel(II)

Conditions

Conditions	Yield
In water Kinetics; reaction of R,S,R,S-Ni(tmc)(1+) with 2-PrCl at 25°C under Cr(2+)-scrubbed Ar;	100%

: 75-29-6
isopropyl chloride

: 1051899-64-9
N2-(3,5-dimorpholinophenyl)-N2-(4-methoxybenzyl)-N4-(3-methoxyphenyl)pyrimidine-2,4-diamine

: 1051899-65-0
N2-(3,5-dimorpholinophenyl)-N4-isopropyl-N2-(4-methoxybenzyl)-N4-(3-methoxyphenyl)pyrimidine-2,4-diamine

Conditions

Conditions	Yield
With sodium hydride In N,N-dimethyl-formamide at 25 - 90℃; for 21h;	100%

: 10599-69-6
5-methyl-2-propionylfuran

: 75-29-6
isopropyl chloride

: 1000993-74-7
1-(4-isopropyl-5-methyl-2-furyl)propan-1-one

Conditions

Conditions	Yield
Stage #1: 5-methyl-2-propionylfuran With aluminum (III) chloride at 0 - 30℃; for 0.5h; Neat (no solvent); Stage #2: isopropyl chloride at 0 - 10℃; Product distribution / selectivity; Neat (no solvent);	100%
Stage #1: 5-methyl-2-propionylfuran With aluminum (III) chloride In dichloromethane at 0 - 35℃; for 0.5h; Stage #2: isopropyl chloride In dichloromethane at 0 - 10℃; for 1h; Industry scale; Stage #3: With sodium hydroxide; water at 0℃; pH=1; Product distribution / selectivity;	100%
Stage #1: 5-methyl-2-propionylfuran With aluminum (III) chloride at 0 - 30℃; for 0.5h; Stage #2: isopropyl chloride at 0 - 10℃; Stage #3: With water at 0℃;

: 75-29-6
isopropyl chloride

: 151266-23-8
4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidine

: 862730-04-9
3-iodo-1-(propan-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 200℃; for 0.0833333h; Microwave irradiation; regioselective reaction;	100%

: 75-29-6
isopropyl chloride

: 14143-26-1
4-hydroxy-2-methylbenzonitrile

: 4-iso-propoxy-2-methylbenzonitrile

Conditions

Conditions	Yield
With tetramethyl ammoniumhydroxide; potassium carbonate In toluene at 25 - 55℃; for 10h; Reagent/catalyst; Temperature;	98.9%

: 75-29-6
isopropyl chloride

: 111757-80-3
(-)-(2S)-trifluoromethanesulfonyloxy-propionic acid tert-butyl ester

: 1059043-99-0
(+)-(2S,3)-dimethyl-butyric acid tert-butyl ester

Conditions

Conditions	Yield
Stage #1: isopropyl chloride With magnesium In tetrahydrofuran Inert atmosphere; Stage #2: (-)-(2S)-trifluoromethanesulfonyloxy-propionic acid tert-butyl ester With zinc(II) chloride In tetrahydrofuran at 0℃; for 3h; Inert atmosphere; optical yield given as %ee; enantiospecific reaction;	98%

: 17771-33-4
7-hydroxy-2,2-dimethyl-chroman-4-one

: 75-29-6
isopropyl chloride

: 120046-15-3
7-Isopropoxy-2,2-dimethyl-chroman-4-one

Conditions

Conditions	Yield
With potassium carbonate; potassium iodide In N,N-dimethyl-formamide at 80℃; for 12h;	96%

: 75-29-6
isopropyl chloride

: 85417-41-0
tris(2,6-dimethoxyphenyl)phosphine

: Tris-(2,6-dimethoxy-phenyl)-isopropyl-phosphonium; perchlorate

Conditions

Conditions	Yield
With perchloric acid In ethanol at 65℃; for 15h;	96%

: 75-29-6
isopropyl chloride

: (C5(CH3)5)Ta(C6H5CCC6H5)(CH3)2

: (C5(CH3)5)Ta(C6H5CCC6H5)(CH3)Cl

Conditions

Conditions	Yield
With AlCl3 In tetrahydrofuran under N2; pinch of AlCl3 added to the soln. of the Ta-complex in THF, addn. of excess i-PrCl at room temp., soln. stirred (8 h); removal of volatiles (vac.), elem. anal.;	96%

: 75-29-6
isopropyl chloride

: 93-55-0
1-phenyl-propan-1-one

: 4397-09-5
2-methyl-3-phenyl-3-pentanol

Conditions

Conditions	Yield
Stage #1: isopropyl chloride; zinc(II) chloride In tetrahydrofuran at 20℃; for 1h; Stage #2: 1-phenyl-propan-1-one In tetrahydrofuran at 0℃; for 2h;	95%
(i) Mg, I2, Et2O, (ii) /BRN= 606215/; Multistep reaction;

: 109-74-0
propyl cyanide

: 75-29-6
isopropyl chloride

: N-Isopropylbutanenitrilium hexachloroantimonate

Conditions

Conditions	Yield
With antimonypentachloride In dichloromethane at 23℃; for 1h;	95%

: 75-29-6
isopropyl chloride

: 1068-55-9
isopropylmagnesium chloride

Conditions

Conditions	Yield
With magnesium In tetrahydrofuran-d8 at 80℃; under 5171.62 Torr; Temperature; Concentration; Inert atmosphere; Flow reactor;	95%
With magnesium In tetrahydrofuran at 21 - 29℃; for 0.5h; Inert atmosphere; Flow reactor;	94.5%
With magnesium In tetrahydrofuran

: 75-29-6
isopropyl chloride

: 91608-15-0
tris(2,4,6-trimethoxyphenyl)phosphine

: Isopropyl-tris-(2,4,6-trimethoxy-phenyl)-phosphonium; perchlorate

Conditions

Conditions	Yield
With perchloric acid In ethanol at 65℃; for 15h;	95%

: 75-29-6
isopropyl chloride

: 19722-76-0
methyl-2,6-dihydroxy-4-methoxybenzoate

: 231621-29-7
2-fluoro-6-methoxy-3-pivaloylbenzonitrile

: 2,4-dihydroxy-6,6'-dimethoxy-2'-fluoro-3-methoxycarbonyl-3'-pivaloyl-benzophenone-N-(2-methylethyl)ketimine

Conditions

Conditions	Yield
Stage #1: isopropyl chloride; 2-fluoro-6-methoxy-3-pivaloylbenzonitrile With antimonypentachloride In dichloromethane for 0.666667h; Stage #2: methyl-2,6-dihydroxy-4-methoxybenzoate In dichloromethane at 20℃; for 2h; Further stages.;	95%

...Expand

polypropyleneglycol: polypropyleneglycol

: 75-29-6
isopropyl chloride

: 140-53-4
p-chlorobenzyl cyanide

: 2012-81-9
3-Methyl-2-(4'-chlorophenyl)-butyronitrile

Conditions

Conditions	Yield
With potassium hydroxide In 5,5-dimethyl-1,3-cyclohexadiene; water	95%

...Expand

: 75-29-6
isopropyl chloride

: 151266-23-8
4-amino-3-iodo-pyrazolo[3,4-d]pyrimidine

: 862730-04-9
3-iodo-1-(propan-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 20 - 200℃; Microwave irradiation;	95%

: 75-29-6
isopropyl chloride

: 14235-81-5
4-Ethynylaniline

: 4-(3-methylbut-1-yn-1-yl)aniline

Conditions

Conditions	Yield
With copper(l) iodide; C21H23ClNiP2S; caesium carbonate; sodium iodide In dimethyl sulfoxide at 50℃; for 12h; Sonogashira Cross-Coupling; Schlenk technique; Inert atmosphere;	95%

: 75-29-6
isopropyl chloride

: 156839-06-4
2-methyldithiocarbazic acid isopropyl ester

Conditions

Conditions	Yield
	94%
	94%

: 75-29-6
isopropyl chloride

: 138526-69-9
3,4,5-trifluoro-1-bromobenzene

: 1310112-87-8
1-bromo-3,4,5-trifluoro-2,6-diisopropylbenzene

Conditions

Conditions	Yield
With aluminum (III) chloride at 0℃; for 3h; Inert atmosphere;	94%
aluminum (III) chloride at 20℃; for 2h; Inert atmosphere;

: 75-29-6
isopropyl chloride

: 4,4,5,5-tetramethyl-2-(2-phenylhexan-2-yl)-1,3,2-dioxaborolane

: (2,3-dimethylheptan-3-yl)benzene

Conditions

Conditions	Yield
With potassium tert-butylate In 1,4-dioxane at 100℃; for 3h; Inert atmosphere; Sealed tube;	94%

2-Chloropropane Standards and Recommendations

DOT Classification: Flammable Liquid; Label: Flammable Liquid

2-Chloropropane Specification

2-Chloropropane is an organic compound with the formula C₃H₇Cl, and its systematic name is the same with the product name. With the CAS registry number 75-29-6, it is also named as Isopropyl chloride. It belongs to the product categories of Organics; Chloro Alkane Compounds. Its EINECS number is 209-187-5. In addition, the molecular weight is 78.54. Its classification code is Mutation data. This chemcial should be sealed and stored in a cool, ventilated and dry place. Moreover, it should be protected from light, heat and fire. This chemical is used as raw material in organic synthetic to prepare pesticide propachlor. It is also used as a solvent.

Physical properties of 2-Chloropropane are: (1)ACD/LogP: 1.976; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 1.98; (4)ACD/LogD (pH 7.4): 1.98; (5)ACD/BCF (pH 5.5): 18.70; (6)ACD/BCF (pH 7.4): 18.70; (7)ACD/KOC (pH 5.5): 283.14; (8)ACD/KOC (pH 7.4): 283.14; (9)#H bond acceptors: 0; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 0; (12)Index of Refraction: 1.379; (13)Molar Refractivity: 20.755 cm³; (14)Molar Volume: 89.817 cm³; (15)Polarizability: 8.228×10^-24cm³; (16)Surface Tension: 18.92 dyne/cm; (17)Density: 0.874 g/cm³; (18)Flash Point: -35 °C; (19)Enthalpy of Vaporization: 27.037 kJ/mol; (20)Boiling Point: 37.254 °C at 760 mmHg; (21)Vapour Pressure: 488.79 mmHg at 25°C.

Preparation of 2-Chloropropane: this chemical can be prepared by propan-2-ol at the temperature 20 °C. This reaction will need reagent chlorotriphenylphosphonium dichlorophosphate. The yield is about 84%.

2-Chloropropane can be prepared by propan-2-ol at the temperature 20 °C

Uses of 2-Chloropropane: it can be used to produce chlorodiethylisopropylsilane at the temperature of 50 °C. It will need reagent Li and solvent petroleum ether with the reaction time of 1 hour. The yield is about 92%.

2-Chloropropane can be used to produce chlorodiethylisopropylsilane at the temperature of 50 °C

When you are using this chemical, please be cautious about it as the following:
This chemcial is extremely flammable, so you should keep it away from sources of ignition - No smoking. It is harmful by inhalation, in contact with skin and if swallowed. This substance is irritating to eyes and respiratory system. You should keep the container in a well-ventilated place, and you must not empty it into drains.

You can still convert the following datas into molecular structure:
(1)SMILES: ClC(C)C
(2)Std. InChI: InChI=1S/C3H7Cl/c1-3(2)4/h3H,1-2H3
(3)Std. InChIKey: ULYZAYCEDJDHCC-UHFFFAOYSA-N

The toxicity data is as follows:

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Effect	Source
mouse	LC50	inhalation	119gm/m³ (119000mg/m³)		Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 55(7), Pg. 93, 1990.
mouse	LD50	oral	1300mg/kg (1300mg/kg)	BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) AUTONOMIC NERVOUS SYSTEM: OTHER (DIRECT) PARASYMPATHOMIMETIC LUNGS, THORAX, OR RESPIRATION: CYANOSIS	Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 55(7), Pg. 93, 1990.
rat	LC50	inhalation	120gm/m³ (120000mg/m³)		Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 55(7), Pg. 93, 1990.
rat	LC50	inhalation	120gm/m³ (120000mg/m³)	BLOOD: CHANGES IN LEUCOCYTE (WBC) COUNT	Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 55(7), Pg. 93, 1990.
rat	LD50	oral	5gm/kg (5000mg/kg)	BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) AUTONOMIC NERVOUS SYSTEM: OTHER (DIRECT) PARASYMPATHOMIMETIC LUNGS, THORAX, OR RESPIRATION: CYANOSIS	Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 55(7), Pg. 93, 1990.

Product Name

Isopropyl chloride

Synthetic route

2-Chloropropane Standards and Recommendations

2-Chloropropane Specification

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