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H7250

Sigma-Aldrich

Histamine dihydrochloride

≥99% (TLC), powder

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Synonym(s):
2-(4-Imidazolyl)ethylamine dihydrochloride
Empirical Formula (Hill Notation):
C5H9N3 · 2HCl
CAS Number:
Molecular Weight:
184.07
Beilstein:
3624116
EC Number:
MDL number:
eCl@ss:
32160406
PubChem Substance ID:

Quality Level

Assay

≥99% (TLC)

form

powder

color

white to off-white

mp

249-252 °C (lit.)

storage temp.

2-8°C

SMILES string

Cl[H].Cl[H].NCCc1c[nH]cn1

InChI

1S/C5H9N3.2ClH/c6-2-1-5-3-7-4-8-5;;/h3-4H,1-2,6H2,(H,7,8);2*1H

InChI key

PPZMYIBUHIPZOS-UHFFFAOYSA-N

Gene Information

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This Item
PHR1357C121509C8707
Histamine dihydrochloride ≥99% (TLC), powder

H7250

Histamine dihydrochloride

-
Supelco

PHR1357

Histamine Dihydrochloride

-
Cystamine dihydrochloride 96%

C121509

Cystamine dihydrochloride

-
Cystamine dihydrochloride BioXtra

C8707

Cystamine dihydrochloride

Premium Grade
assay

≥99% (TLC)

assay

-

assay

96%

assay

≥98% (TLC)

Quality Level

200

Quality Level

300

Quality Level

200

Quality Level

200

storage temp.

2-8°C

storage temp.

2-30°C

storage temp.

-

storage temp.

-

color

white to off-white

color

-

color

-

color

-

mp

249-252 °C (lit.)

mp

-

mp

217-220 °C (dec.) (lit.)

mp

217-220 °C (dec.) (lit.)

General description

Histamine dihydrochloride is a derivative of histamine. It prevents the formation of ROS (reactive oxygen species), which inhibits the activation of T cells and natural killer cells. Histamine dihydrochloride is implicated in tumor cell apoptosis. It prevents the relapse of acute myeloid leukemia in patients.

Application

Histamine dihydrochloride has been used:
  • as a orthograde cotransmitter in producing excitatory postsynaptic potential (EPSP)
  • to determine its level in fish using HPLC (high performance liquid chromatography)
  • to assess the tracheal response to antigens in guinea-pigs

Features and Benefits

This compound is a featured product for Neuroscience research. Click here to discover more featured Neuroscience products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
This compound is featured on the Histamine Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Pictograms

Exclamation markHealth hazard

Signal Word

Danger

Hazard Classifications

Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Customers Also Viewed

Slide 1 of 4

1 of 4

Immunotherapy with histamine dihydrochloride for the prevention of relapse in acute myeloid leukemia
Martner A, et al.
Expert Review of Hematology, 3(4), 381-391 (2010)
Histamine H4 receptor: a Novel Drug Target For Immunoregulation and Inflammation (2013)
Maternal dietary antigens and the immune response in the offspring of the guinea-pig.
Telemo E, et al.
Immunology, 62(1), 35-35 (1987)
Nitric oxide as an orthograde cotransmitter at central synapses of Aplysia: responses of isolated neurons in culture
Jacklet JW and Koh HY
American Zoologist, 41(2), 282-291 (2001)
Andrej Ščavničar et al.
Journal of AOAC International, 101(5), 1542-1547 (2018-03-25)
A new method for determination of underivatized biogenic amines in cheese based on ion exchange chromatography coupled with tandem mass spectrometric detection was proposed. The method was applied to the analysis of 10 biogenic amines (trimethylamine, putrescine, cadaverine, histamine, 2-phenylethylamine

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