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ChemicalBook >> CAS DataBase List >>1,3,5-TRIBROMOADAMANTANE

1,3,5-TRIBROMOADAMANTANE

CAS No.
707-34-6
Chemical Name:
1,3,5-TRIBROMOADAMANTANE
Synonyms
SALOR-INT L496510-1EA;LABOTEST-BB LT00077082;1,3,5-Tribromoadamentane;1,3,5-TRIBROMOADAMANTANE;Carboxyamidotriazole Impurity 7;(1s,3s,5s)-1,3,5-tribromoadamantane*;Tricyclo[3.3.1.13,7]decane, 1,3,5-tribromo-
CBNumber:
CB8292777
Molecular Formula:
C10H13Br3
Molecular Weight:
372.92
MDL Number:
MFCD00167847
MOL File:
707-34-6.mol
MSDS File:
SDS
Last updated:2026-05-28 03:46:22
Product description Number Pack Size Price
1,3,5-Tribromoadamantane FT66958 250mg $150
1,3,5-Tribromoadamantane FT66958 100mg $150
1,3,5-Tribromoadamantane FT66958 500mg $175
1,3,5-Tribromoadamantane FT66958 1000mg $520
1,3,5-Tribromoadamantane 311792 50.00mg $65
More product size

1,3,5-TRIBROMOADAMANTANE Properties

Melting point 126-127℃ (hexane )
Boiling point 329.0±22.0 °C(Predicted)
Density 2.235±0.06 g/cm3 (20 ºC 760 Torr)
storage temp. Sealed in dry,Room Temperature
Appearance White to off-white Solid

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P280-P305+P351+P338

1,3,5-TRIBROMOADAMANTANE price More Price(36)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth FT66958 1,3,5-Tribromoadamantane 707-34-6 250mg $150 2026-06-04 Buy
Biosynth FT66958 1,3,5-Tribromoadamantane 707-34-6 100mg $150 2026-06-04 Buy
Biosynth FT66958 1,3,5-Tribromoadamantane 707-34-6 500mg $175 2026-06-04 Buy
Biosynth FT66958 1,3,5-Tribromoadamantane 707-34-6 1000mg $520 2026-06-04 Buy
Matrix Scientific 311792 1,3,5-Tribromoadamantane 707-34-6 50.00mg $65 2026-05-19 Buy
Product number Packaging Price Buy
FT66958 250mg $150 Buy
FT66958 100mg $150 Buy
FT66958 500mg $175 Buy
FT66958 1000mg $520 Buy
311792 50.00mg $65 Buy

1,3,5-TRIBROMOADAMANTANE Chemical Properties,Uses,Production

Uses

1,3,5-Tribromoadamantane is an brominated impurity of Memantine (M218000), an antiparkinsonian and antispasmodic agent.

Synthesis

Adamantane

281-23-2

1,3,5-TRIBROMOADAMANTANE

707-34-6

Step 1: In a 5L four-necked reaction flask equipped with a condenser, thermometer, and tail gas absorption device, slowly add 108 g of iron powder dropwise to 400 mL of anhydrous bromine for about half an hour. After the dropwise addition was completed, stirring was continued for 30 minutes. Step 2: Slowly add the remaining bromine dropwise to the reaction flask. After completion of the dropwise addition, the reaction system was heated to 45-50 °C, and then 600 g of adamantane was slowly added. The reaction temperature was raised to 62-65°C to reflux. The reaction lasted for 65 h, during which time samples were taken for GC analysis to monitor feedstock consumption (control experiment 1). The molar ratio of adamantane, anhydrous bromine and iron powder was 1:10.6:0.44. Step 3: After completion of the reaction, bromine was recovered by distillation. The reaction mixture was poured into ice containing 3.5 L of chloroform, stirred for 10 minutes, and then filtered through a diatomaceous earth pad. Step 4: The filtrate was washed with saturated aqueous sodium bisulfite to consume excess bromine (note cooling). Use 5 kg of solid sodium bisulfite for washing. Step 5: The organic layer was washed twice with water, using 3kg of water each time. After washing, the organic layer was concentrated to dryness to give 1.95kg of crude product. Step 6: The crude product was dissolved in 13L of methanol and heated until dissolved. 65g of activated carbon was added and filtered hot. The filtrate was crystallized with stirring (cooled with ice) and filtered to give 1.19kg of product. The mother liquor was concentrated to about one-third of the original volume, crystallized again with stirring, and filtered to obtain 250g of white fine powder.

References

[1] Chemische Berichte, 1960, vol. 93, p. 1366 - 1371
[2] Journal of Organic Chemistry, 2004, vol. 69, # 4, p. 1010 - 1019
[3] Chemistry - An Asian Journal, 2011, vol. 6, # 6, p. 1450 - 1455
[4] Journal of Organic Chemistry, 2014, vol. 79, # 14, p. 6738 - 6742
[5] Patent: CN104628526, 2016, B. Location in patent: Paragraph 0069-0075

1,3,5-TRIBROMOADAMANTANE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 77)Suppliers
Supplier Tel Email Country ProdList Advantage
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View Lastest Price from 1,3,5-TRIBROMOADAMANTANE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
1,3,5-TRIBROMOADAMANTANE pictures 2020-01-10 1,3,5-TRIBROMOADAMANTANE
707-34-6
1KG 98%; 99% 500g;1kg; 25kg Career Henan Chemical Co

1,3,5-TRIBROMOADAMANTANE Spectrum

SALOR-INT L496510-1EA LABOTEST-BB LT00077082 1,3,5-TRIBROMOADAMANTANE 1,3,5-Tribromoadamentane (1s,3s,5s)-1,3,5-tribromoadamantane* Tricyclo[3.3.1.13,7]decane, 1,3,5-tribromo- Carboxyamidotriazole Impurity 7 707-34-6 C10H13Br3 Adamantane derivatives
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