Chlorobutanol hemihydrate structure
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Common Name | Chlorobutanol hemihydrate | ||
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CAS Number | 6001-64-5 | Molecular Weight | 372.929 | |
Density | N/A | Boiling Point | 167ºC | |
Molecular Formula | C4H9Cl3O2 | Melting Point | 75-79ºC | |
MSDS | Chinese USA | Flash Point | 100ºC | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of Chlorobutanol hemihydrateChlorobutanol hemihydrate is a pharmaceutical preservative with sedative-hypnotic actions. Chlorobutanol hemihydrate is active against a wide variety of Gram-positive and Gram-negative bacteria, and several mold spores and fungi. Chlorobutanol hemihydrate is widely used in food and cosmetic industry[1][2]. |
Name | 1,1,1-Trichloro-2-Methyl-2-Propanol Hemihydrate |
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Synonym | More Synonyms |
Description | Chlorobutanol hemihydrate is a pharmaceutical preservative with sedative-hypnotic actions. Chlorobutanol hemihydrate is active against a wide variety of Gram-positive and Gram-negative bacteria, and several mold spores and fungi. Chlorobutanol hemihydrate is widely used in food and cosmetic industry[1][2]. |
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Related Catalog | |
References |
Boiling Point | 167ºC |
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Melting Point | 75-79ºC |
Molecular Formula | C4H9Cl3O2 |
Molecular Weight | 372.929 |
Flash Point | 100ºC |
Exact Mass | 369.923065 |
PSA | 29.46000 |
LogP | 2.06320 |
Appearance of Characters | Crystalline Powder, Crystals and/or Chunks | White to almost white |
Storage condition | -20°C |
Stability | Stable. Generates toxic fumes on combustion. Incompatible with strong oxidizing agents. |
Water Solubility | Slightly soluble in water, very soluble in ethanol (96 per cent), soluble in glycerol (85 per cent). | Soluble in ethanol, ether, chloroform, and glycerol. Insoluble in water. |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302 |
Precautionary Statements | P301 + P312 + P330 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xn:Harmful; |
Risk Phrases | R22;R36/37/38 |
Safety Phrases | 26-36/37/39 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | UC0175000 |
An efficient synthesis of a dual PPAR alpha/gamma agonist and the formation of a sterically congested alpha-aryloxyisobutyric acid via a Bargellini reaction.
J. Org. Chem. 70(21) , 8560-3, (2005) A practical synthesis of benzisoxazole 1 and its conversion to alpha-aryloxyisobutyric acid 2 using 1,1,1-trichloro-2-methyl-2-propanol (chloretone) was developed. Benzisoxazole 1 was formed in high y... |
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Application of a capillary electrophoresis method for simultaneous determination of preservatives in pharmaceutical formulations.
J. Sep. Sci. 28(2) , 137-43, (2005) Preservatives are used to protect pharmaceutical formulations from microbial attack during the period of administration to the patient. Because of their biological activity, preservatives have to be i... |
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Freeze-drying above room temperature.
J. Pharm. Sci. 88(5) , 501-6, (1999) This study investigates the use of solid, organic compounds to lyophilize drugs without conventional freeze-drying equipment. The aim of the investigation is to find a pharmaceutically acceptable solv... |
1,1,1-Trichloro-2-methyl-2-propanol hemihydrate |
1,1,1-Trichloro-2-methyl-2-propanol hydrate (2:1) |
MFCD02179352 |
1,1,1-trichloro-2-methyl-2-propanol(hydrate) (2:1) |
Chlorobutanol Hemihydrate |
1,1,1-Trichloro-2-methylpropan-2-ol hydrate (2:1) |
2-Propanol, 1,1,1-trichloro-2-methyl-, hydrate (2:1) |