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PHENTERMINE HYDROCHLORIDE

Product Name
PHENTERMINE HYDROCHLORIDE
CAS No.
1197-21-3
Chemical Name
PHENTERMINE HYDROCHLORIDE
Synonyms
Fastin;Adipex-p;Oby-Trim;Phenteral;Dea no. 1640;Phentermine HCL;Einecs 214-821-9;wilpohydrochloride;Phentermyl Wyncaps;PHENTERMINE HYDROCHLORIDE
CBNumber
CB9419722
Molecular Formula
C10H16ClN
Formula Weight
185.69
MOL File
1197-21-3.mol
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PHENTERMINE HYDROCHLORIDE Property

Melting point:
200-201℃
solubility 
DMF: 3 mg/ml; DMSO: 5 mg/ml; Ethanol: 20 mg/ml; PBS (pH 7.2): 5 mg/ml
form 
A neat solid
Merck 
13,7346
CAS DataBase Reference
1197-21-3(CAS DataBase Reference)
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Safety

Hazard Codes 
T,Xi
Risk Statements 
25
Safety Statements 
22-26-36/37-45
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
3
RTECS 
SH4950000
Hazard Note 
Irritant
HS Code 
2921460000
Toxicity
mouse,LD50,oral,154mg/kg (154mg/kg),Toxicology and Applied Pharmacology. Vol. 3, Pg. 256, 1961.
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H301Toxic if swalloed

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

P405Store locked up.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
1528501
Product name
Phentermine hydrochloride
Purity
United States Pharmacopeia (USP) Reference Standard
Packaging
200mg
Price
$581
Updated
2024/03/01
Cayman Chemical
Product number
14207
Product name
Phentermine (hydrochloride)
Purity
≥98%
Packaging
1mg
Price
$21
Updated
2024/03/01
Cayman Chemical
Product number
14207
Product name
Phentermine (hydrochloride)
Purity
≥98%
Packaging
10mg
Price
$50
Updated
2024/03/01
Cayman Chemical
Product number
ISO60198
Product name
Phentermine (hydrochloride) (CRM)
Packaging
1mg
Price
$21
Updated
2024/03/01
AK Scientific
Product number
4308CA
Product name
Phentermine hydrochloride
Packaging
1mg
Price
$121
Updated
2021/12/16
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PHENTERMINE HYDROCHLORIDE Chemical Properties,Usage,Production

Chemical Properties

White Solid

Originator

Wilpo ,Dorsey, US,1961

Uses

Controlled substance (stimulant). Anorexic. An Amphetamine derivative.

Manufacturing Process

Preparation of isobutyrophenone: In a 12 liter, 3-necked flask, 1,280 grams of aluminum chloride was covered with 2,000 cc of dry thiophene-free benzene and a solution of 919 grams of isobutyryl chloride, (BP 92°-94°C) in 1 liter of benzene was added slowly with stirring. After heating for 3 hours at reflux, the solution was cooled and poured over a mixture of 1 liter of concentrated hydrochloric acid and 5 kg of ice. The benzene layer was separated, the aqueous layer extracted with benzene, and the combined benzene solutions were washed, dried and concentrated in vacuo. The residue was distilled rapidly to give 1,051 grams of isobutyrophenone, boiling at 81°-89°C at 1 mm, yield 83.4%.
Preparation of 1,3-Diphenyl-2,2-Dimethylpropanone-1: Sodamide was prepared from 12.5 grams of sodium added in small portions to 600 cc of liquid ammonia with 1 gram of hydrous ferric chloride as catalyst. The ammonia was replaced by 200 cc of dry toluene and without delay a solution of 74 grams of isobutyrophenone and 76.5 grams of benzyl bromide in 200 cc of benzene was slowly added with stirring. The reaction mixture was heated on a boiling water bath for 48 hours. Water was then added, the organic layer separated and the product isolated by distillation. The 1,3-diphenyl-2,2 Phentermine dimethylpropanone-1 boiled from 142°-143°C at a pressure of 3 mm, nD201.5652.
Preparation of α,α-Dimethyl-β-Phenylpropionamide: Sodamide was prepared from 7.6 grams of sodium in 350 cc of liquid ammonia with 0.9 gram of hydrous ferric chloride. The ammonia was replaced by 250 cc of toluene, the mixture was heated to 60°C and 71.4 grams of 1,3-diphenyl-2,2-dimethyl propanone-1 dissolved in 150 cc of toluene was added. The mixture was stirred and heated on a steam bath for 5 hours. A clear red color appeared in 15 minutes and disappeared after about an hour. After cooling, water was added, the organic layer was washed, dried, and concentrated to give 36.5 grams of α,α-dimethyl-β-phenyl propionamide which crystallized slowly after the addition of an equal volume of petroleum ether. The product melted at 62°C after crystallization from benzene-petroleum ether.
Preparation of Di-(β-Phenyl-α,α-Dimethylethyl)Urea: 3.5 grams of α,αdimethyl-β-phenylpropionamide in 420 cc of water was added to a solution of 87.5 grams of potassium hydroxide and 35 grams of bromine in 350 cc of water. After 2 hours at 60°C, the product was obtained on crystallization from ethanol, melting at 184°C.
Preparation of ω-Phenyl-tert-Butylamine: 24 grams of the urea derivative obtained as indicated above, were well mixed with 96 grams of calcium hydroxide in a flask immersed in an air bath and provided with a dropping funnel the stem of which reached the bottom of the flask. The mixture was heated to 240°-260°C (inside temperature) for 7 hours during which time 86 cc of water was slowly added. The vapors were collected in a receiver cooled with ice. After extraction with ether and distillation, the product was obtained as a colorless liquid boiling from 80°-84°C at 9 mm according to US Patent 2,590,079.
The ether solution may be dried and saturated with hydrogen chloride and the precipitated hydrochloride recrystallized from a mixture of 50 parts alcohol and 100 parts of acetone.
The pure hydrochloride is thus obtained as a white crystalline substance having a MP of 195°-196°C, according to US Patent 2,408,345.

brand name

Adipex-P(Teva); Fastin (GlaxoSmithKline).

Therapeutic Function

Antiobesity

PHENTERMINE HYDROCHLORIDE Preparation Products And Raw materials

Raw materials

Preparation Products

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PHENTERMINE HYDROCHLORIDE Suppliers

Spectrum Chemical Manufacturing Corp.
Tel
021-021-021-67601398-809-809-809 15221380277
Fax
021-57711696
Email
marketing_china@spectrumchemical.com
Country
China
ProdList
9658
Advantage
60
HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
Chizhou Kailong Import and Export Trade Co., Ltd.
Tel
Fax
-
Email
xg01_gj@163.com
Country
China
ProdList
9484
Advantage
50
Nanjing Peiwill Biotechnology Co.,Ltd.
Tel
025-57027729 15850702895
Fax
025-57027729
Email
15850702895@163.com
Country
China
ProdList
71
Advantage
55
Nanjing crow LuNing pharmaceutical technology co., LTD
Tel
13382066392
Country
CHINA
ProdList
4877
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32063
Advantage
58
Chemwill Asia Co.,Ltd.
Tel
86-21-51086038
Fax
86-21-51861608
Email
chemwill_asia@126.com
Country
CHINA
ProdList
23912
Advantage
58
Changzhou Furuisi Biotechnology Co., Ltd
Tel
0519-85524369
Email
3477467573@qq.com
Country
China
ProdList
8617
Advantage
58
Shandong Tianming Biotechnology Development Co. Ltd
Tel
400-9019001
Country
China
ProdList
15069
Advantage
58
LGC Science (Shanghai) Ltd.
Tel
17717235263
Email
cindy.yang@lgcgroup.com
Country
China
ProdList
14734
Advantage
58

1197-21-3, PHENTERMINE HYDROCHLORIDERelated Search:


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