Thiamine hydrochloride
tested according to Ph. Eur.
Manufacturer: Sigma Aldrich
CAS Number: 67-03-8
Synonym(S): Thiamio hydrochloridum, Aneurine hydrochloride, Vitamin B1 hydrochloride
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 50 G | 04573-50-G | In Stock | ₹ 5,986.23 |
04573 - 50 G
In Stock
Quantity
1
Base Price: ₹ 5,986.23
GST (18%): ₹ 1,077.521
Total Price: ₹ 7,063.751
biological source
synthetic
Quality Level
200
Agency
USP/NFtested according to Ph. Eur.
Assay
98.5-101.0% anhydrous basis
form
solid
mp
250 °C (dec.) (lit.)
solubility
alcohol: soluble 1 gm in 100 ml (95%)alcohol: soluble 1 gm in 315 ml (Absolute)glycerol: soluble 1 gm in 18 mlwater: soluble 1 g/mLbenzene: insolublechloroform: insolublediethyl ether: insolublehexane: insolublemethanol: very solublepropylene glycol: soluble
storage temp.
2-8°C
SMILES string
CC1=NC(N)=C(C[N+]2=CSC(CCO)=C2C)C=N1.Cl.[Cl-]
InChI
1S/C12H17N4OS.2ClH/c1-8-11(3-4-17)18-7-16(8)6-10-5-14-9(2)15-12(10)13;;/h5,7,17H,3-4,6H2,1-2H3,(H2,13,14,15);2*1H/q+1;;/p-1
Other Options
Related Products
Description
- Application: Thiamine hydrochloride has been used as a keratin salts medium supplement for culturing log-phase fungus.[1] It has also been used as a supplement of VB medium the minimal medium of Vogel and Bonner.[2]
- Biochem/physiol Actions: Thiamine hydrochloride is a cheap, non-toxic and efficient catalyst for the synthesis of amidoalkyl naphthols.[3] It inhibits the production of shikonin derivatives by suspension cultures of Lithospermum erythrorhizon.[4] Additionally, thiamine hydrochloride addition to apple juice concentrates reduces its patulin content.[5]
SAFETY INFORMATION
Pictograms
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Compare Similar Items
Show Difference
biological source: synthetic
Quality Level: 200
Agency: USP/NFtested according to Ph. Eur.
Assay: 98.5-101.0% anhydrous basis
form: solid
mp: 250 °C (dec.) (lit.)
solubility: alcohol: soluble 1 gm in 100 ml (95%)alcohol: soluble 1 gm in 315 ml (Absolute)glycerol: soluble 1 gm in 18 mlwater: soluble 1 g/mLbenzene: insolublechloroform: insolublediethyl ether: insolublehexane: insolublemethanol: very solublepropylene glycol: soluble
storage temp.: 2-8°C
SMILES string: CC1=NC(N)=C(C[N+]2=CSC(CCO)=C2C)C=N1.Cl.[Cl-]
InChI: 1S/C12H17N4OS.2ClH/c1-8-11(3-4-17)18-7-16(8)6-10-5-14-9(2)15-12(10)13;;/h5,7,17H,3-4,6H2,1-2H3,(H2,13,14,15);2*1H/q+1;;/p-1
biological source: __
Quality Level: __
Agency: __
Assay: __
form: __
mp: __
solubility: __
storage temp.: −20°C
SMILES string: C[C@@H]1CCc2c(C)coc2C1
InChI: 1S/C10H14O/c1-7-3-4-9-8(2)6-11-10(9)5-7/h6-7H,3-5H2,1-2H3/t7-/m1/s1
biological source: __
Quality Level: 300
Agency: __
Assay: __
form: powder
mp: __
solubility: __
storage temp.: __
SMILES string: C[C@H]1O[C@H](C[C@H](O)[C@@H]1O)O[C@H]2[C@@H](O)C[C@@H](O[C@@H]2C)O[C@H]3[C@@H](O)C[C@@H](O[C@@H]3C)O[C@H]4CC[C@@]5(C)[C@H](CC[C@@H]6[C@@H]5C[C@@H](O)[C@]7(C)[C@H](CC[C@]67O)C8=CC(=O)OC8)C4
InChI: 1S/C41H64O14/c1-19-36(47)28(42)15-34(50-19)54-38-21(3)52-35(17-30(38)44)55-37-20(2)51-33(16-29(37)43)53-24-8-10-39(4)23(13-24)6-7-26-27(39)14-31(45)40(5)25(9-11-41(26,40)48)22-12-32(46)49-18-22/h12,19-21,23-31,33-38,42-45,47-48H,6-11,13-18H2,1-5H3/t19-,20-,21-,23-,24+,25-,26-,27+,28+,29+,30+,31-,33+,34+,35+,36-,37-,38-,39+,40+,41+/m1/s1