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  • 4261-67-0 Structure
  • Basic information

    1. Product Name: 3-Dimethylamino-2-methylpropyl chloride hydrochloride
    2. Synonyms: GAMMA-DIMETHYL-AMINO-ISOBUTYL CHLORIDE HCL;DIMETHYLAMINOMETHYLPROPYL CHLORIDE HCL;3-DIMETHYLAMINO-2-METHYLPROPYL CHLORIDE HYDROCHLORIDE;3-CHLORO-N,N,2-TRIMETHYLPROPYLAMINE HYDROCHLORIDE;1-CHLORO-2-METHYL-3-DIMETHYLAMINOPROPANE HYDROCHLORIDE;1-Dimethylamino-2-methyl-3-chloropropane HCL (DMMPC, HCl);3-Chloro-2-methyl-N,N-dimethylpropylamine hydrochloride;3-chloro-2-methylpropyl(dimethyl)ammonium chloride
    3. CAS NO:4261-67-0
    4. Molecular Formula: C6H14ClN*ClH
    5. Molecular Weight: 172.1
    6. EINECS: 224-237-6
    7. Product Categories: Amines;Intermediates & Fine Chemicals;Pharmaceuticals
    8. Mol File: 4261-67-0.mol
    9. Article Data: 1
  • Chemical Properties

    1. Melting Point: 169-173 °C
    2. Boiling Point: 144.5 °C at 760 mmHg
    3. Flash Point: 41.2 °C
    4. Appearance: White to off-white/Powder
    5. Density: N/A
    6. Vapor Pressure: 5.07mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    9. Solubility: N/A
    10. Sensitive: Hygroscopic
    11. BRN: 4444785
    12. CAS DataBase Reference: 3-Dimethylamino-2-methylpropyl chloride hydrochloride(CAS DataBase Reference)
    13. NIST Chemistry Reference: 3-Dimethylamino-2-methylpropyl chloride hydrochloride(4261-67-0)
    14. EPA Substance Registry System: 3-Dimethylamino-2-methylpropyl chloride hydrochloride(4261-67-0)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 37/39-26
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 4261-67-0(Hazardous Substances Data)

4261-67-0 Usage

Chemical Properties

white to off-white powder

Uses

Cyamemazine intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 4261-67-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,6 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4261-67:
(6*4)+(5*2)+(4*6)+(3*1)+(2*6)+(1*7)=80
80 % 10 = 0
So 4261-67-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H14ClN/c1-6(4-7)5-8(2)3/h6H,4-5H2,1-3H3/p+1/t6-/m0/s1

4261-67-0 Well-known Company Product Price

  • Brand
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  • Detail
  • Alfa Aesar

  • (L06091)  3-Dimethylamino-2-methylpropyl chloride hydrochloride, 98%   

  • 4261-67-0

  • 25g

  • 202.0CNY

  • Detail
  • Alfa Aesar

  • (L06091)  3-Dimethylamino-2-methylpropyl chloride hydrochloride, 98%   

  • 4261-67-0

  • 100g

  • 671.0CNY

  • Detail
  • Alfa Aesar

  • (L06091)  3-Dimethylamino-2-methylpropyl chloride hydrochloride, 98%   

  • 4261-67-0

  • 500g

  • 2608.0CNY

  • Detail

4261-67-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Dimethylamino-2-methylpropyl chloride hydrochloride

1.2 Other means of identification

Product number -
Other names 3-chloro-N,N,2-trimethylpropan-1-amine,hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4261-67-0 SDS

4261-67-0Synthetic route

2-methyl-3-dimethylaminopropanol
33622-41-2

2-methyl-3-dimethylaminopropanol

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

Conditions
ConditionsYield
With thionyl chloride In chloroform Reflux; Cooling with ice;
10H-dipyrido[3,4-b:3',4'-e][1,4]thiazine
503321-47-9

10H-dipyrido[3,4-b:3',4'-e][1,4]thiazine

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

10-(3'-dimethylamino-2'-methylpropyl)-2,7-diazaphenothiazine

10-(3'-dimethylamino-2'-methylpropyl)-2,7-diazaphenothiazine

Conditions
ConditionsYield
With sodium hydroxide In 1,4-dioxane for 5h; Heating;84%
5H-dipyrido[2,3-b:4',3'-e][1,4]thiazine

5H-dipyrido[2,3-b:4',3'-e][1,4]thiazine

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

10-(3'-dimethylamino-2'-methylpropyl)-3,6-diazaphenothiazine

10-(3'-dimethylamino-2'-methylpropyl)-3,6-diazaphenothiazine

Conditions
ConditionsYield
Stage #1: 5H-dipyrido[2,3-b:4',3'-e][1,4]thiazine With sodium hydroxide In 1,4-dioxane for 2h; Reflux;
Stage #2: 1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride In 1,4-dioxane for 24h; Reflux;
82%
6H-9-chloroquino[3,2-b]benzo[1,4]thiazine
1192303-44-8

6H-9-chloroquino[3,2-b]benzo[1,4]thiazine

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

6-(3-dimethylamino-2-methylpropyl)-9-chloroquinobenzothiazine
1443133-98-9

6-(3-dimethylamino-2-methylpropyl)-9-chloroquinobenzothiazine

Conditions
ConditionsYield
With sodium hydroxide In 1,4-dioxane for 3h; Reflux;78%
9-methylthio-6H-quinobenzothiazine
1192303-47-1

9-methylthio-6H-quinobenzothiazine

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

6-(3-dimethylamino-2-methylpropyl)-9-methylthioquinobenzothiazine
1443133-99-0

6-(3-dimethylamino-2-methylpropyl)-9-methylthioquinobenzothiazine

Conditions
ConditionsYield
With sodium hydroxide In 1,4-dioxane for 3h; Reflux;76%
6H-quino[3,2-b]benzo[1,4]thiazine
158438-85-8

6H-quino[3,2-b]benzo[1,4]thiazine

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

6-(3-dimethylamino-2-methylpropyl)quinobenzothiazine
1443133-97-8

6-(3-dimethylamino-2-methylpropyl)quinobenzothiazine

Conditions
ConditionsYield
With sodium hydroxide In 1,4-dioxane for 3h; Reflux;74%
6H-9-fluoroquinobenzothiazine
1192303-46-0

6H-9-fluoroquinobenzothiazine

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

C21H22FN3S

C21H22FN3S

Conditions
ConditionsYield
With sodium hydroxide for 3h; Reflux;71%
6H-diquino[3,2-b;2',3'-e][1,4]thiazine
911371-11-4

6H-diquino[3,2-b;2',3'-e][1,4]thiazine

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

6-(3'-dimethylamino-2'-methylpropyl)diquinothiazine
1027333-79-4

6-(3'-dimethylamino-2'-methylpropyl)diquinothiazine

Conditions
ConditionsYield
With sodium hydroxide In 1,4-dioxane for 3h; Heating;62%
1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

1-azido-2-methyl-3-(N,N-dimethylamino)propane

1-azido-2-methyl-3-(N,N-dimethylamino)propane

Conditions
ConditionsYield
With sodium azide In water at 80℃; for 15h;45%
With sodium azide In water at 80℃;45%
1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

1-benzyl-3-hydroxy-1H-indazole
2215-63-6

1-benzyl-3-hydroxy-1H-indazole

[3-(1-benzyl-1H-indazol-3-yloxy)-2-methyl-propyl]-dimethyl-amine

[3-(1-benzyl-1H-indazol-3-yloxy)-2-methyl-propyl]-dimethyl-amine

Conditions
ConditionsYield
Stage #1: 1-benzyl-3-hydroxy-1H-indazole With sodium hydride In N,N-dimethyl-formamide at 20℃; for 0.5h;
Stage #2: 1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride With sodium hydride In N,N-dimethyl-formamide at 100℃; for 12h; Further stages.;
45%
1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

(3-Dimethylamino-2-methyl-propyl)-hydrazin
89600-39-5

(3-Dimethylamino-2-methyl-propyl)-hydrazin

Conditions
ConditionsYield
(i) N2H4*H2O, (ii) K2CO3; Multistep reaction;
1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

1,1-Bis-(3-dimethylamino-2-methyl-propyl)-hydrazin
91695-34-0

1,1-Bis-(3-dimethylamino-2-methyl-propyl)-hydrazin

Conditions
ConditionsYield
(i) N2H4*H2O, (ii) K2CO3; Multistep reaction;
2,7-dihydroxy-9H-fluoren-9-one
42523-29-5

2,7-dihydroxy-9H-fluoren-9-one

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

2,7-Bis-(3-dimethylamino-2-methyl-propoxy)-fluoren-9-one

2,7-Bis-(3-dimethylamino-2-methyl-propoxy)-fluoren-9-one

Conditions
ConditionsYield
With potassium hydroxide In toluene
1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

7-chloro-3-(3,5-dimethylphenyl)-4-hydroxy-1H-quinolin-2-one
142326-67-8

7-chloro-3-(3,5-dimethylphenyl)-4-hydroxy-1H-quinolin-2-one

7-chloro-4-(3-dimethylamino-2-methyl-propoxy)-3-(3,5-dimethyl-phenyl)-1H-quinolin-2-one

7-chloro-4-(3-dimethylamino-2-methyl-propoxy)-3-(3,5-dimethyl-phenyl)-1H-quinolin-2-one

Conditions
ConditionsYield
With potassium carbonate; sodium iodide In N,N-dimethyl-formamide at 80℃; for 16h; Alkylation;
1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

Phenyl-2-propanon-(2-methyl-3-dimethylamino-propylhydrazon)
106458-88-2

Phenyl-2-propanon-(2-methyl-3-dimethylamino-propylhydrazon)

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: (i) N2H4*H2O, (ii) K2CO3
2: benzene / Heating
View Scheme
1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

1-(2-Methyl-3-dimethylaminopropyl)-2-(1-phenyl-2-propyl)hydrazin
92793-44-7

1-(2-Methyl-3-dimethylaminopropyl)-2-(1-phenyl-2-propyl)hydrazin

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: (i) N2H4*H2O, (ii) K2CO3
2: benzene / Heating
3: LiAlH4 / diethyl ether / Heating
View Scheme
2,3-dihydro-3-hydroxy-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one
27068-88-8

2,3-dihydro-3-hydroxy-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one

diethyl ether
60-29-7

diethyl ether

water
7732-18-5

water

potassium carbonate
584-08-7

potassium carbonate

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

Cis(+)-3-acetyloxy-2,3-dihydro-5-(2-methyl-3-dimethylaminopropyl)-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one oxalate

Cis(+)-3-acetyloxy-2,3-dihydro-5-(2-methyl-3-dimethylaminopropyl)-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one oxalate

Conditions
ConditionsYield
With oxalic acid; acetic anhydride In acetone
1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

3-(dimethylamino)-2-methylpropyl carbamimidothioate dihydrochloride
118646-15-4

3-(dimethylamino)-2-methylpropyl carbamimidothioate dihydrochloride

Conditions
ConditionsYield
With thiourea In ethanol; calcium chloride
sodium hydride-mineral oil

sodium hydride-mineral oil

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

4,9-Dihydro-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one
56276-59-6

4,9-Dihydro-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one

9-(3-Dimethylamino-2-methylpropyl)-4,9-dihydro-4-methyl-10H-thieno[3,4-b] [1,5]benzodiazepin-10-one, hydrochloride
59720-16-0

9-(3-Dimethylamino-2-methylpropyl)-4,9-dihydro-4-methyl-10H-thieno[3,4-b] [1,5]benzodiazepin-10-one, hydrochloride

Conditions
ConditionsYield
In N-methyl-acetamide; benzene
1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

m,p-dichloroaniline
95-76-1

m,p-dichloroaniline

N'-(3,4-dichlorophenyl)-N,N,2-trimethylpropane-1,3-diamine

N'-(3,4-dichlorophenyl)-N,N,2-trimethylpropane-1,3-diamine

Conditions
ConditionsYield
With sodium hydroxide
N-(5-chloro-pyrimidin-2-yl)-acetamide
68303-37-7

N-(5-chloro-pyrimidin-2-yl)-acetamide

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

2-(2-methyl-3-dimethylaminopropylamino)-5-chloropyrimidine

2-(2-methyl-3-dimethylaminopropylamino)-5-chloropyrimidine

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

N,N-dimethyl-N'-(2-methyl-3-dimethylaminopropyl)-N'-(5-chloro-2-pyrimidinyl)urea

N,N-dimethyl-N'-(2-methyl-3-dimethylaminopropyl)-N'-(5-chloro-2-pyrimidinyl)urea

maleic anhydride
108-31-6

maleic anhydride

1-dodecyl alcohol
112-53-8

1-dodecyl alcohol

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride
4261-67-0

1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride

C22H41NO4

C22H41NO4

Conditions
ConditionsYield
Stage #1: maleic anhydride; 1-dodecyl alcohol In n-heptane at 15 - 80℃; for 6h;
Stage #2: With 18-crown-6 ether; potassium carbonate In chloroform at 60℃; for 4h;
Stage #3: 1-chloro-2-methyl-3-(dimethylamino)propane hydrochloride In chloroform at 50℃; for 20h;

4261-67-0Relevant articles and documents

Side chain impacts on pH- and thermo-responsiveness of tertiary amine functionalized polypeptides

Xiao, Chunsheng,Cheng, Yilong,Zhang, Yu,Ding, Jianxun,He, Chaoliang,Zhuang, Xiuli,Chen, Xuesi

, p. 671 - 679 (2014)

The systemic investigation of the structural impacts of side chains on the pH- and thermo-responsiveness of tertiary amine functionalized poly(l-glutamate)s (TA-PGs) was carried out. The TA-PGs polymers were effectively synthesized by Cu(I)-catalyzed azide-alkyne cycloaddition click reaction of azido tertiary amines with poly(γ-propargyl-l-glutamate) (PPLG). Turbimetric measurements were performed to characterize the pH- and temperature-induced phase transition of TA-PGs in aqueous solution, which suggested a structural dependence of the properties on the N-substituted groups and the "linkers" between 1,2,3-triazole ring and the tertiary amine groups in the side chains. In detail, the pH responsive properties of TA-PGs were basically determined by the hydrophobicity of the N-substituted groups in the side chains and the pH transition point (pHt) decreased as the increasing hydrophobicity of the N-substituted groups, while the temperature-responsiveness of TA-PGs were affected by either the N-substituted groups or the "linkers." TA-PGs with a moderate N-substituted amine group (e.g., DEA, PR, and PD) or a branched "linker" (e.g., iso-propylene and 2-methylpropylene group) were more likely to express the LCST-type phase transition tuned by pH variation. These structure-property relationships revealed in this study would help to develop the applications of TA-PGs in smart drug delivery systems. Copyright

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